This document discusses various air-based hazards and methods for managing critical hazards. It begins by listing sources of air pollution such as various industries, households, agricultural practices, construction activities, volcanic eruptions, and more. It then discusses heating, ventilation, and air conditioning (HVAC) systems for pharmaceutical plants. Next, it covers preliminary hazard analysis and its purpose and benefits. It also discusses the fire prevention triangle of heat, oxygen, and fuel. The document provides advice on managing each of these elements to prevent fires. It describes various types of fire extinguishers and their appropriate uses. Finally, it discusses the key elements of a critical hazard management system including identifying hazards, risk assessment, and implementing control measures.
Effective process validation contributes significantly to assuring drug quality. The basic
principle of quality assurance is that a drug should be produced that is fit for its intended use.
This principle incorporates the understanding that the following conditions exist:
• Quality, safety, and efficacy are designed or built into the product.
• Quality cannot be adequately assured merely by in-process and finished-product
inspection or testing
This presentation explains about qualifications of HPTLC, types of qualifications, design qualification , installation qualification ,operational qualification, performance qualification ,documentation of qualification .
This document discusses the qualification of manufacturing equipment. It explains that equipment qualification is necessary to ensure equipment works correctly and produces reliable results. There are four types of qualification: design, installation, operational, and performance. Design qualification defines equipment specifications. Installation qualification confirms proper installation. Operational qualification verifies equipment functions as specified. Performance qualification demonstrates consistent performance under routine use. The document then provides details on specific qualification procedures for dry powder mixers and fluidized bed dryers.
Role of quality system and audits in pharmamaceuticalganpat420
Introduction
cGMP Regulations
Quality Assurance Function
Quality Systems Approach
Management Responsibilities
Resources
Manufacturing Operations
Evaluation Activities
Transitioning to Quality Systems Approach
Audit Checklist for Drug Industry
The document discusses the qualification of high performance thin layer chromatography (HPTLC). It describes the four types of qualification: design qualification, installation qualification, operation qualification, and performance qualification. Design qualification verifies specifications and review methods. Installation qualification documents compliance at installation. Operation qualification documents consistent performance within operating ranges. Performance qualification ascertains the instrument is suitable for specific analytical tasks. The document then provides examples of tests to check HPTLC performance, including linearity of spotting, reproducibility of spotting, and detection capacity.
Auditing of Granulation Operation in Dry Production AreaPritam Kolge
Auditing of Granulation Operation in Dry Production Area.....
This topic comes under Audits and Regulatory Compliance....
This is useful for M.Pharm (Pharaceutical Quality Assurance) Students who studying in First year sem II....
This Presentation Contain following...
#Objectives
#Fundamentals of Granulation
#Reasons for Granulation
#Methods of Granulation
#Agglomeration
#Fundamentals and Audit of Dry Granulation
#Steps in Dry Granulation
#Fundamentals and Audit of Fluid Bed Granulation
#Scale-Up of Fluid bed Granulation
#High share granulation-Fundamentals, Audit and Scale-Up
#Overview and Comparison of Different Granulating Techniques
#Audit of Mixing and Blending, Wet granulation, Wet milling, Drying, Milling
#Conclusion
#References
Thanks For Help and Guidance of Mr. D.P.Mali Sir
Effective process validation contributes significantly to assuring drug quality. The basic
principle of quality assurance is that a drug should be produced that is fit for its intended use.
This principle incorporates the understanding that the following conditions exist:
• Quality, safety, and efficacy are designed or built into the product.
• Quality cannot be adequately assured merely by in-process and finished-product
inspection or testing
This presentation explains about qualifications of HPTLC, types of qualifications, design qualification , installation qualification ,operational qualification, performance qualification ,documentation of qualification .
This document discusses the qualification of manufacturing equipment. It explains that equipment qualification is necessary to ensure equipment works correctly and produces reliable results. There are four types of qualification: design, installation, operational, and performance. Design qualification defines equipment specifications. Installation qualification confirms proper installation. Operational qualification verifies equipment functions as specified. Performance qualification demonstrates consistent performance under routine use. The document then provides details on specific qualification procedures for dry powder mixers and fluidized bed dryers.
Role of quality system and audits in pharmamaceuticalganpat420
Introduction
cGMP Regulations
Quality Assurance Function
Quality Systems Approach
Management Responsibilities
Resources
Manufacturing Operations
Evaluation Activities
Transitioning to Quality Systems Approach
Audit Checklist for Drug Industry
The document discusses the qualification of high performance thin layer chromatography (HPTLC). It describes the four types of qualification: design qualification, installation qualification, operation qualification, and performance qualification. Design qualification verifies specifications and review methods. Installation qualification documents compliance at installation. Operation qualification documents consistent performance within operating ranges. Performance qualification ascertains the instrument is suitable for specific analytical tasks. The document then provides examples of tests to check HPTLC performance, including linearity of spotting, reproducibility of spotting, and detection capacity.
Auditing of Granulation Operation in Dry Production AreaPritam Kolge
Auditing of Granulation Operation in Dry Production Area.....
This topic comes under Audits and Regulatory Compliance....
This is useful for M.Pharm (Pharaceutical Quality Assurance) Students who studying in First year sem II....
This Presentation Contain following...
#Objectives
#Fundamentals of Granulation
#Reasons for Granulation
#Methods of Granulation
#Agglomeration
#Fundamentals and Audit of Dry Granulation
#Steps in Dry Granulation
#Fundamentals and Audit of Fluid Bed Granulation
#Scale-Up of Fluid bed Granulation
#High share granulation-Fundamentals, Audit and Scale-Up
#Overview and Comparison of Different Granulating Techniques
#Audit of Mixing and Blending, Wet granulation, Wet milling, Drying, Milling
#Conclusion
#References
Thanks For Help and Guidance of Mr. D.P.Mali Sir
The document summarizes validation of an HVAC system for a pharmaceutical facility. It discusses the importance of HVAC systems in cleanrooms and outlines some key validation parameters to test, including:
1. Airflow pattern, velocity, and changes per hour to ensure proper airflow.
2. Filter leak testing and particulate counting to check filter performance and air quality.
3. Pressure differential, temperature, humidity, and sound level testing to validate environmental controls.
Validation of the HVAC system is necessary to demonstrate that it can consistently supply air meeting quality standards to maintain aseptic manufacturing conditions.
The document discusses air-based hazards and fire protection. It describes various sources of air pollution like combustion of fuels, industrial processes, and natural sources. Specific pollutants from these sources like carbon monoxide, heavy metals, nitrogen oxides, and particulate matter are discussed. The effects of air hazards like smog, soot, greenhouse gases, and pollen are also summarized. The document then covers air circulation maintenance in sterile and non-sterile areas, preliminary hazard analysis procedures, and classifications of fire.
This document provides information on aseptic processing technology and quality control testing for various sterile pharmaceutical dosage forms including ointments, suspensions, emulsions, and sterile solutions. It discusses cleanroom classifications, manufacturing processes, and in-process quality control tests for content uniformity, clarity, leakage, extractable volume, sterility, consistency, penetration, irritation potential, sedimentation, redispersibility, particle size, viscosity, and zeta potential.
This document provides information about vendor qualification procedures in the pharmaceutical industry. It begins with definitions of key terms like vendor and qualification. It then describes the types of vendors, including business-to-business and business-to-customer. It outlines a classification system for vendors from Category 1 to 4 based on risk. The document details the seven steps for vendor selection and qualification procedures for raw material and packaging material vendors. It provides guidance on inclusion of vendors in the approved vendor list and reasons for exclusion from the list, along with corrective actions.
In this slide contains details about Pharmaceutical validation of water system
Presented by: K VENKATSAI PRASAD (Department of pharmaceutical analysis and quality assurance).RIPER, anantapur
This document discusses in-process quality control (IPQC) tests for ointments. It describes IPQC as the process of controlling quality parameters during manufacturing from raw materials to final packaging. It then lists and describes 11 common IPQC tests conducted on ointments, including tests for appearance, drug content, pH, sensitivity, spreadability, absorption rate, extrudability, sterility, viscosity, medicament release rate, and uniformity of weight. The tests are designed to ensure the quality, safety and efficacy of ointment products during production.
USFDA guidelines on process validation a life cycle approachRx Ayush Sharma
The document summarizes the US FDA's 2011 guidance on process validation, which outlines a lifecycle approach. It discusses the three stages of process validation according to the guidance: (1) Process Design which defines the commercial process based on development, (2) Process Qualification which evaluates the process's capability for commercial manufacturing, and (3) Continued Process Verification which gains ongoing assurance that the process remains in control during routine production. The lifecycle approach integrates validation strategies from previous guidelines and emphasizes continual process improvement, understanding sources of variation, and controlling variation to ensure consistent quality.
The document discusses the qualification of analytical equipment like electronic balances and pH meters. It explains that qualification includes design, installation, operational and performance qualification to ensure equipment is properly installed and functioning accurately. Specific steps for qualifying balances, such as daily calibration checks with internal weights and yearly checks with external weights, are provided. The two-point calibration method for pH meters using buffer solutions is also described. Acceptance limits and record keeping procedures are outlined to ensure equipment remains calibrated over time.
Quality by Design and Process Analytical TechnologyMANIKANDAN V
This document discusses Quality by Design (QbD) and Process Analytical Technology (PAT) as applied to the pharmaceutical industry. It defines key QbD concepts like Quality Target Product Profile, Critical Quality Attributes, Critical Material Attributes, Critical Process Parameters, and design space. It explains how QbD involves systematic development through risk assessment and control strategies to consistently deliver quality products. PAT is described as using real-time measurements and process monitoring to ensure quality and facilitate continuous improvement. The roles of QbD and PAT in drug development and manufacturing are also summarized.
This document discusses the process validation of capsules. It begins by providing background on validation and defining process validation according to the FDA. It then describes the three main types of process validation: prospective, concurrent, and retrospective. Key documents used in validation like the validation master plan, validation protocols and reports, and standard operating procedures are also outlined. The validation process for capsules is then detailed, including evaluating the capsule composition, selecting the encapsulation process and equipment, and testing the encapsulation step. Critical factors considered during encapsulation like the technique used and encapsulation speed are also summarized.
Fluidized Bed Dryer
Principle of FBD
Construction of FBD
Working of FBD
Steps of Fluidization
Qualification of FBD
Design Qualification
Installation Qualification
Operational Qualification
Performance Qualification
References
This document discusses the validation of processes for manufacturing oral liquid dosage forms such as solutions, suspensions, and emulsions. It covers the stages of process validation, objectives of validation for liquids which include ensuring the product meets specifications. Key aspects that are validated include equipment, raw materials, the manufacturing process, product specifications, stability, and packaging. Parameters tested include appearance, pH, viscosity, specific gravity, microbial count, content uniformity, and dissolution. The document provides details on validation of these parameters and criteria for acceptance.
This document discusses the qualification of dissolution test apparatus and validation of utility systems. It covers the installation qualification, operational qualification, and performance qualification of dissolution test apparatus. This includes procedures, acceptance criteria, and maintenance schedules for qualifying the apparatus. It also summarizes validation test functions and acceptance criteria for key utility systems like plant steam, pure steam, water for injection, and emergency power generators. The goal is to ensure dissolution testing provides reliable and reproducible results for assessing drug release and bioavailability.
Air circulation maintenance industry for sterile and non sterile areaGNIPST
The document discusses the importance of air circulation maintenance systems in the pharmaceutical manufacturing industry. Properly designed and maintained air handling systems are critical to ensuring sterile and non-sterile manufacturing areas meet quality standards by controlling airborne particulates, temperature, humidity and air pressure. Various filters are used to clean air entering production rooms from either fresh external air sources or re-circulated internal air. Documentation of installation, operation, maintenance and monitoring of air handling systems is required as part of validation and compliance with cGMP regulations.
This document provides an overview of facility design considerations for advanced sterile product manufacturing. It discusses key areas like area planning based on product type, facility classification, environmental control zones, wall and floor treatments, change rooms, personnel flow, and utility locations. Proper facility design with controlled environments and aseptic practices is necessary to ensure sterility of pharmaceutical products like APIs, antibiotics, and biological products during manufacturing.
It is process of “Establishing documentary evidence that provide a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality attributes”.
In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products, it is also assured that the process will consistently produce the expected results.
Validation is action of proving in accordance with the principles of good manufacturing practices, that any procedure, process, equipment, material, activity or system actually leads to expected results.
Cleaning validation is documented evidence with a high degree assurance that one can consistently clean a system or a piece of equipment to predetermined and acceptable limits.
The primary regulatory concern driving the need for cleaning validation is cross contamination of the desired drug substance either by other API from previous batch runs or by residues from the cleaning agents used.
The prime purpose of validating a cleaning process is to ensure compliance with federal and other standard regulations
1. Cross contamination with active ingredients
Contamination of one batch of product with significant levels of residual active ingredients from previous batch cannot be tolerated.
In addition to the obvious problems posed by subjecting consumers or patients to unintended contaminants, potential clinically significant synergistic interactions between pharmacologically active chemicals are a real concern.
2. Contamination with unintended materials or compounds
While inert ingredients used in drug products are generally recognized as safe for human consumption, the routine use, maintenance and cleaning of equipment's provide the potential contamination with such items as equipment parts, lubricants and chemical cleaning agents3. Microbiological contamination
Maintenance , cleaning and storage conditions may provide adventitious microorganisms with the opportunity to proliferate within the processing equipment.
The document discusses fire safety and prevention. It covers developing an emergency action plan and fire prevention plan as required by OSHA. The emergency action plan must include procedures for evacuation, accounting for employees, and reporting emergencies. The fire prevention plan must identify hazards and responsibilities. Fire hazards discussed include electrical, office equipment, cutting and welding, and flammable materials. It also outlines requirements for alarm systems, fixed extinguishing systems, and portable fire extinguishers. Management and employees must be trained on the plans and equipment maintained.
The document summarizes validation of an HVAC system for a pharmaceutical facility. It discusses the importance of HVAC systems in cleanrooms and outlines some key validation parameters to test, including:
1. Airflow pattern, velocity, and changes per hour to ensure proper airflow.
2. Filter leak testing and particulate counting to check filter performance and air quality.
3. Pressure differential, temperature, humidity, and sound level testing to validate environmental controls.
Validation of the HVAC system is necessary to demonstrate that it can consistently supply air meeting quality standards to maintain aseptic manufacturing conditions.
The document discusses air-based hazards and fire protection. It describes various sources of air pollution like combustion of fuels, industrial processes, and natural sources. Specific pollutants from these sources like carbon monoxide, heavy metals, nitrogen oxides, and particulate matter are discussed. The effects of air hazards like smog, soot, greenhouse gases, and pollen are also summarized. The document then covers air circulation maintenance in sterile and non-sterile areas, preliminary hazard analysis procedures, and classifications of fire.
This document provides information on aseptic processing technology and quality control testing for various sterile pharmaceutical dosage forms including ointments, suspensions, emulsions, and sterile solutions. It discusses cleanroom classifications, manufacturing processes, and in-process quality control tests for content uniformity, clarity, leakage, extractable volume, sterility, consistency, penetration, irritation potential, sedimentation, redispersibility, particle size, viscosity, and zeta potential.
This document provides information about vendor qualification procedures in the pharmaceutical industry. It begins with definitions of key terms like vendor and qualification. It then describes the types of vendors, including business-to-business and business-to-customer. It outlines a classification system for vendors from Category 1 to 4 based on risk. The document details the seven steps for vendor selection and qualification procedures for raw material and packaging material vendors. It provides guidance on inclusion of vendors in the approved vendor list and reasons for exclusion from the list, along with corrective actions.
In this slide contains details about Pharmaceutical validation of water system
Presented by: K VENKATSAI PRASAD (Department of pharmaceutical analysis and quality assurance).RIPER, anantapur
This document discusses in-process quality control (IPQC) tests for ointments. It describes IPQC as the process of controlling quality parameters during manufacturing from raw materials to final packaging. It then lists and describes 11 common IPQC tests conducted on ointments, including tests for appearance, drug content, pH, sensitivity, spreadability, absorption rate, extrudability, sterility, viscosity, medicament release rate, and uniformity of weight. The tests are designed to ensure the quality, safety and efficacy of ointment products during production.
USFDA guidelines on process validation a life cycle approachRx Ayush Sharma
The document summarizes the US FDA's 2011 guidance on process validation, which outlines a lifecycle approach. It discusses the three stages of process validation according to the guidance: (1) Process Design which defines the commercial process based on development, (2) Process Qualification which evaluates the process's capability for commercial manufacturing, and (3) Continued Process Verification which gains ongoing assurance that the process remains in control during routine production. The lifecycle approach integrates validation strategies from previous guidelines and emphasizes continual process improvement, understanding sources of variation, and controlling variation to ensure consistent quality.
The document discusses the qualification of analytical equipment like electronic balances and pH meters. It explains that qualification includes design, installation, operational and performance qualification to ensure equipment is properly installed and functioning accurately. Specific steps for qualifying balances, such as daily calibration checks with internal weights and yearly checks with external weights, are provided. The two-point calibration method for pH meters using buffer solutions is also described. Acceptance limits and record keeping procedures are outlined to ensure equipment remains calibrated over time.
Quality by Design and Process Analytical TechnologyMANIKANDAN V
This document discusses Quality by Design (QbD) and Process Analytical Technology (PAT) as applied to the pharmaceutical industry. It defines key QbD concepts like Quality Target Product Profile, Critical Quality Attributes, Critical Material Attributes, Critical Process Parameters, and design space. It explains how QbD involves systematic development through risk assessment and control strategies to consistently deliver quality products. PAT is described as using real-time measurements and process monitoring to ensure quality and facilitate continuous improvement. The roles of QbD and PAT in drug development and manufacturing are also summarized.
This document discusses the process validation of capsules. It begins by providing background on validation and defining process validation according to the FDA. It then describes the three main types of process validation: prospective, concurrent, and retrospective. Key documents used in validation like the validation master plan, validation protocols and reports, and standard operating procedures are also outlined. The validation process for capsules is then detailed, including evaluating the capsule composition, selecting the encapsulation process and equipment, and testing the encapsulation step. Critical factors considered during encapsulation like the technique used and encapsulation speed are also summarized.
Fluidized Bed Dryer
Principle of FBD
Construction of FBD
Working of FBD
Steps of Fluidization
Qualification of FBD
Design Qualification
Installation Qualification
Operational Qualification
Performance Qualification
References
This document discusses the validation of processes for manufacturing oral liquid dosage forms such as solutions, suspensions, and emulsions. It covers the stages of process validation, objectives of validation for liquids which include ensuring the product meets specifications. Key aspects that are validated include equipment, raw materials, the manufacturing process, product specifications, stability, and packaging. Parameters tested include appearance, pH, viscosity, specific gravity, microbial count, content uniformity, and dissolution. The document provides details on validation of these parameters and criteria for acceptance.
This document discusses the qualification of dissolution test apparatus and validation of utility systems. It covers the installation qualification, operational qualification, and performance qualification of dissolution test apparatus. This includes procedures, acceptance criteria, and maintenance schedules for qualifying the apparatus. It also summarizes validation test functions and acceptance criteria for key utility systems like plant steam, pure steam, water for injection, and emergency power generators. The goal is to ensure dissolution testing provides reliable and reproducible results for assessing drug release and bioavailability.
Air circulation maintenance industry for sterile and non sterile areaGNIPST
The document discusses the importance of air circulation maintenance systems in the pharmaceutical manufacturing industry. Properly designed and maintained air handling systems are critical to ensuring sterile and non-sterile manufacturing areas meet quality standards by controlling airborne particulates, temperature, humidity and air pressure. Various filters are used to clean air entering production rooms from either fresh external air sources or re-circulated internal air. Documentation of installation, operation, maintenance and monitoring of air handling systems is required as part of validation and compliance with cGMP regulations.
This document provides an overview of facility design considerations for advanced sterile product manufacturing. It discusses key areas like area planning based on product type, facility classification, environmental control zones, wall and floor treatments, change rooms, personnel flow, and utility locations. Proper facility design with controlled environments and aseptic practices is necessary to ensure sterility of pharmaceutical products like APIs, antibiotics, and biological products during manufacturing.
It is process of “Establishing documentary evidence that provide a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality attributes”.
In the pharmaceutical industry, it is very important that in addition to final testing and compliance of products, it is also assured that the process will consistently produce the expected results.
Validation is action of proving in accordance with the principles of good manufacturing practices, that any procedure, process, equipment, material, activity or system actually leads to expected results.
Cleaning validation is documented evidence with a high degree assurance that one can consistently clean a system or a piece of equipment to predetermined and acceptable limits.
The primary regulatory concern driving the need for cleaning validation is cross contamination of the desired drug substance either by other API from previous batch runs or by residues from the cleaning agents used.
The prime purpose of validating a cleaning process is to ensure compliance with federal and other standard regulations
1. Cross contamination with active ingredients
Contamination of one batch of product with significant levels of residual active ingredients from previous batch cannot be tolerated.
In addition to the obvious problems posed by subjecting consumers or patients to unintended contaminants, potential clinically significant synergistic interactions between pharmacologically active chemicals are a real concern.
2. Contamination with unintended materials or compounds
While inert ingredients used in drug products are generally recognized as safe for human consumption, the routine use, maintenance and cleaning of equipment's provide the potential contamination with such items as equipment parts, lubricants and chemical cleaning agents3. Microbiological contamination
Maintenance , cleaning and storage conditions may provide adventitious microorganisms with the opportunity to proliferate within the processing equipment.
The document discusses fire safety and prevention. It covers developing an emergency action plan and fire prevention plan as required by OSHA. The emergency action plan must include procedures for evacuation, accounting for employees, and reporting emergencies. The fire prevention plan must identify hazards and responsibilities. Fire hazards discussed include electrical, office equipment, cutting and welding, and flammable materials. It also outlines requirements for alarm systems, fixed extinguishing systems, and portable fire extinguishers. Management and employees must be trained on the plans and equipment maintained.
This document summarizes key information about managing hazardous chemicals in the workplace according to Australian legislation. It outlines duties of various parties to identify hazards, implement controls, safely handle, store and dispose of chemicals. Specific requirements around classification, labeling, safety data sheets, registers and health monitoring are discussed. The goals are to increase understanding of chemical hazards and ensure appropriate safety controls are in place.
Toxic materials can harm the body if they enter through skin absorption, inhalation, ingestion, or injection. Effects may be acute like immediate reactions, or chronic like delayed health issues. Common toxic groups include dusts, fumes, gases, solvents, metals, acids, bases, and pesticides. To minimize hazards, proper storage, handling, ventilation, protective equipment, worker training, and waste disposal are needed. Hazard identification numbers and symbols communicate toxicity dangers.
Laura Engells completed an internship with the Environment, Health and Safety (EHS) Department at Freescale Semiconductor. Over the summer of 2015, she worked on several projects under the guidance of her mentor Troy Wappler. These projects included creating training materials on chemical handling, developing emergency response charts, drafting a fire impairment checklist, writing a process safety management report, and organizing documents for an air permit. Engells gained experience in areas like hazards analysis, manufacturing processes, and technical writing from her work on these projects.
The document outlines a site-specific environmental management plan (SSEMP) for a construction project. The SSEMP aims to identify potential environmental impacts from construction activities and put in place measures to control or avoid them. It defines roles and responsibilities for environmental management and procedures for reporting, training, auditing and site management. The SSEMP also covers hazard identification and mitigation measures for different hazard types, an emergency response plan, and a traffic management plan to ensure safety during construction vehicle movement.
The document discusses various topics related to process plant safety including material handling safety, chemical plant design, piping and instrumentation diagrams, control systems, alarms, equipment and piping design, passive and active protections, emergency shutdown systems, and inherent safety techniques. It provides details on factors to consider for safe material handling, guidelines for chemical plant layout and design, symbols used in P&IDs, designing alarm and control systems, and methods to build safety into chemical plant design.
This document discusses safety and loss prevention in process design. It identifies potential hazards associated with chemical processes such as toxicity, flammability, pressure, temperature deviation, noise, and sources of ignition. It discusses measuring and controlling hazards to prevent dangerous deviations. Methods to control hazards include containment, ventilation, disposal, and emergency equipment. Hazard and Operability Studies (HAZOP) are introduced as a way to identify hazards and operability problems in a process design or operating plant. Intrinsic and extrinsic safety are also discussed.
1) Firefighting involves extinguishing fires to protect lives and property. It requires professional training to develop skills in firefighting techniques and specialist operations.
2) Hotels must have basic safety equipment like smoke detectors, fire extinguishers, carbon monoxide detectors, and accident prevention signs to protect guests. This includes smoke detectors in all rooms and public areas, appropriately classified fire extinguishers, and signs clearly indicating dangers and emergency exits.
3) Proper organization, training, equipment, and protective clothing are needed for effective fire brigade operations in hotels. Fire brigades must be trained prior to assignment and regularly to perform interior structural firefighting safely.
This document summarizes key safety policies and procedures for working in a laboratory setting. It outlines hazards like chemicals, electricity, fire, and machinery. It emphasizes having proper training and using personal protective equipment. The document also provides guidance on chemical hygiene plans, material safety data sheets, chemical storage, handling spills, first aid for exposures, and safe practices for compressed gas cylinders. The overall goal is to prevent accidents and injuries by making safety the top priority in laboratory work.
The document discusses various workplace safety regulations and hazards. It covers proper procedures for dealing with accidents, fires and emergencies. Personal protective equipment should be used correctly according to organizational policies. The top industries for workplace accidents are listed as service, construction, retail and manufacturing. Job hazards like tripping, electrical, and chemical risks should be addressed. Health hazards from illness spread and proper hygiene are also covered. The document outlines policies for reporting incidents, evacuation, decontamination, waste disposal and management, and electrical and fire safety. Ensuring safety regulations, training, and professionalism can help protect workers.
The presentation is about hazard identification as against hazard assessment. The need to comply with all standard safety procedures as outlined by OSHA
Like manufacturers in all industries, pharmaceutical manufacturers and their employees face real and serious health and safety issues. In some cases, the hazards are the same ones we find in most manufacturing facilities. In other cases, the hazards are more specific to pharmaceutical manufacturing. Likewise, pharmaceutical manufacturers use hazard controls and risk mitigations that are common to many industries as well as more specific to pharmaceutical manufacturing, including all levels of the hierarchy of controls, from elimination down to administrative controls such as training for pharmaceutical safety and the use of PPE.
This document provides an overview of key laboratory safety topics, including:
- The hierarchy of controls for hazards and types of engineering, administrative and personal protective controls.
- Chemical, biological and physical hazards like noise, radiation and ergonomics. It outlines exposure limits and safety measures.
- Requirements for chemical hygiene plans, exposure monitoring, medical exams, hazard communication, and more.
- Best practices for working with research animals, managing change, conducting safety training, and chemical inventory control.
- Examples of incidents involving water-reactive chemicals and lack of proper protective equipment emphasize importance of compliance.
The document provides information on environmental management plans (EMPs), including their objectives, elements, and principles. An EMP is required to formulate, implement, and monitor environmental protection measures for projects. It must include details on proposed/implemented mitigation measures and associated costs. Environmental aspects should be considered at all project stages from conceptualization to operation. The management plan should be based on resource conservation and pollution prevention considerations like effluents, air/noise pollution, wastes, health and safety, and more. Monitoring programs are also established to track environmental parameters. Overall, the EMP helps ensure regulatory compliance and continuous improvement of environmental performance.
Industrial technology and Accidents, clean technology, Clean Development Mech...H. M. Touhidul Islam
Industrial Technology, Technological development in industry, Industrial Accidents in Factory, Types of Accident in Factory, Causes of Accidents in factory, Monitoring and protecting measure of Industrial Accidents, Safe Toxic Waste management, Waste Disposal Technology, What is clean technology, Clean Development Mechanism (CDM) & CDM Scenario in Bangladesh, mitigation and adaptation measures in CDM concept, National plan on sustainable habitual action concept of CDM, Green Architecture Issues of energy security
This document discusses reaction progress kinetic analysis and strategies for selecting optimal and cost-effective routes for scale-up synthesis. It notes that route selection considers environmental impact, legal intellectual property, economics, control over product quality specifications, and throughput. Expedient routes are employed early in drug development to expedite material for testing and consider familiarity, technical feasibility, and equipment availability. Characteristics of cost-effective routes include technical feasibility, suitable equipment, and availability of inexpensive reagents and starting materials. The document provides examples of reagent and solvent selection strategies and families of reagents useful for scale-up, such as bases, oxidations, and catalytic reagents.
The document summarizes various health and safety hazards associated with the marijuana production industry. It discusses biological, chemical, physical, and other risks to workers and recommends safety precautions. With legalization expanding, it is important to properly train workers and implement regulations to protect them, as in other industries. A Colorado committee published a guide to help marijuana employers recognize hazards and establish safety programs.
The technology uses reclaimed CO₂ as the dyeing medium in a closed loop process. When pressurized, CO₂ becomes supercritical (SC-CO₂). In this state CO₂ has a very high solvent power, allowing the dye to dissolve easily.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/
The debris of the ‘last major merger’ is dynamically youngSérgio Sacani
The Milky Way’s (MW) inner stellar halo contains an [Fe/H]-rich component with highly eccentric orbits, often referred to as the
‘last major merger.’ Hypotheses for the origin of this component include Gaia-Sausage/Enceladus (GSE), where the progenitor
collided with the MW proto-disc 8–11 Gyr ago, and the Virgo Radial Merger (VRM), where the progenitor collided with the
MW disc within the last 3 Gyr. These two scenarios make different predictions about observable structure in local phase space,
because the morphology of debris depends on how long it has had to phase mix. The recently identified phase-space folds in Gaia
DR3 have positive caustic velocities, making them fundamentally different than the phase-mixed chevrons found in simulations
at late times. Roughly 20 per cent of the stars in the prograde local stellar halo are associated with the observed caustics. Based
on a simple phase-mixing model, the observed number of caustics are consistent with a merger that occurred 1–2 Gyr ago.
We also compare the observed phase-space distribution to FIRE-2 Latte simulations of GSE-like mergers, using a quantitative
measurement of phase mixing (2D causticality). The observed local phase-space distribution best matches the simulated data
1–2 Gyr after collision, and certainly not later than 3 Gyr. This is further evidence that the progenitor of the ‘last major merger’
did not collide with the MW proto-disc at early times, as is thought for the GSE, but instead collided with the MW disc within
the last few Gyr, consistent with the body of work surrounding the VRM.
Unlocking the mysteries of reproduction: Exploring fecundity and gonadosomati...AbdullaAlAsif1
The pygmy halfbeak Dermogenys colletei, is known for its viviparous nature, this presents an intriguing case of relatively low fecundity, raising questions about potential compensatory reproductive strategies employed by this species. Our study delves into the examination of fecundity and the Gonadosomatic Index (GSI) in the Pygmy Halfbeak, D. colletei (Meisner, 2001), an intriguing viviparous fish indigenous to Sarawak, Borneo. We hypothesize that the Pygmy halfbeak, D. colletei, may exhibit unique reproductive adaptations to offset its low fecundity, thus enhancing its survival and fitness. To address this, we conducted a comprehensive study utilizing 28 mature female specimens of D. colletei, carefully measuring fecundity and GSI to shed light on the reproductive adaptations of this species. Our findings reveal that D. colletei indeed exhibits low fecundity, with a mean of 16.76 ± 2.01, and a mean GSI of 12.83 ± 1.27, providing crucial insights into the reproductive mechanisms at play in this species. These results underscore the existence of unique reproductive strategies in D. colletei, enabling its adaptation and persistence in Borneo's diverse aquatic ecosystems, and call for further ecological research to elucidate these mechanisms. This study lends to a better understanding of viviparous fish in Borneo and contributes to the broader field of aquatic ecology, enhancing our knowledge of species adaptations to unique ecological challenges.
Or: Beyond linear.
Abstract: Equivariant neural networks are neural networks that incorporate symmetries. The nonlinear activation functions in these networks result in interesting nonlinear equivariant maps between simple representations, and motivate the key player of this talk: piecewise linear representation theory.
Disclaimer: No one is perfect, so please mind that there might be mistakes and typos.
dtubbenhauer@gmail.com
Corrected slides: dtubbenhauer.com/talks.html
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
ESPP presentation to EU Waste Water Network, 4th June 2024 “EU policies driving nutrient removal and recycling
and the revised UWWTD (Urban Waste Water Treatment Directive)”
ESR spectroscopy in liquid food and beverages.pptxPRIYANKA PATEL
With increasing population, people need to rely on packaged food stuffs. Packaging of food materials requires the preservation of food. There are various methods for the treatment of food to preserve them and irradiation treatment of food is one of them. It is the most common and the most harmless method for the food preservation as it does not alter the necessary micronutrients of food materials. Although irradiated food doesn’t cause any harm to the human health but still the quality assessment of food is required to provide consumers with necessary information about the food. ESR spectroscopy is the most sophisticated way to investigate the quality of the food and the free radicals induced during the processing of the food. ESR spin trapping technique is useful for the detection of highly unstable radicals in the food. The antioxidant capability of liquid food and beverages in mainly performed by spin trapping technique.
Immersive Learning That Works: Research Grounding and Paths ForwardLeonel Morgado
We will metaverse into the essence of immersive learning, into its three dimensions and conceptual models. This approach encompasses elements from teaching methodologies to social involvement, through organizational concerns and technologies. Challenging the perception of learning as knowledge transfer, we introduce a 'Uses, Practices & Strategies' model operationalized by the 'Immersive Learning Brain' and ‘Immersion Cube’ frameworks. This approach offers a comprehensive guide through the intricacies of immersive educational experiences and spotlighting research frontiers, along the immersion dimensions of system, narrative, and agency. Our discourse extends to stakeholders beyond the academic sphere, addressing the interests of technologists, instructional designers, and policymakers. We span various contexts, from formal education to organizational transformation to the new horizon of an AI-pervasive society. This keynote aims to unite the iLRN community in a collaborative journey towards a future where immersive learning research and practice coalesce, paving the way for innovative educational research and practice landscapes.
Describing and Interpreting an Immersive Learning Case with the Immersion Cub...Leonel Morgado
Current descriptions of immersive learning cases are often difficult or impossible to compare. This is due to a myriad of different options on what details to include, which aspects are relevant, and on the descriptive approaches employed. Also, these aspects often combine very specific details with more general guidelines or indicate intents and rationales without clarifying their implementation. In this paper we provide a method to describe immersive learning cases that is structured to enable comparisons, yet flexible enough to allow researchers and practitioners to decide which aspects to include. This method leverages a taxonomy that classifies educational aspects at three levels (uses, practices, and strategies) and then utilizes two frameworks, the Immersive Learning Brain and the Immersion Cube, to enable a structured description and interpretation of immersive learning cases. The method is then demonstrated on a published immersive learning case on training for wind turbine maintenance using virtual reality. Applying the method results in a structured artifact, the Immersive Learning Case Sheet, that tags the case with its proximal uses, practices, and strategies, and refines the free text case description to ensure that matching details are included. This contribution is thus a case description method in support of future comparative research of immersive learning cases. We then discuss how the resulting description and interpretation can be leveraged to change immersion learning cases, by enriching them (considering low-effort changes or additions) or innovating (exploring more challenging avenues of transformation). The method holds significant promise to support better-grounded research in immersive learning.
1. UNIT:2 AIR BASED
HAZARDS(EHTESHAM)
SOURCES:-
1. Industry: The majority of industries depend on fossil fuels in one way or another, and as a result, they
generate CO and CO2, sulphar hexafluoride, and particulate matter. The main source of environmental
particulate matter emissions is the cement industry. A variety of dangerous volatile substances are
released from paint, electronics, dry cleaning products, and decrying agents. Moreover, the use of HFC,
Nitrogen Oxides, and Sulfur produces pollutants.
2. Households: Here, it is possible to take into account carbon and soot emissions from cooking with
fossil fuels. Permethrin molecules from insecticides, for example, are volatile toxicants that can
contaminate food or the air and cause poisoning.
3. Agricultural practises:- Practices in agriculture, like the usage of organic fertilizer , contribute to the
emission of greenhouse gases. POP are pollutants that are released by pesticides. Methane is the
primary greenhouse gas produced during enteric fermentation in the cattle ranching industry. Air quality
is also reduced by the toxic chemicals present in herbicides and pesticides.
4. Land mining, earth moving activity, and quarrying: These processes include extracting substantial
mineral resources from the earth, which results in the release of toxic compounds such as dust
Blasphemy and limestone quarrying Dust particles are produced during the manufacture of cement.
simplest particles.
5. Construction and repair projects:- Activities including drilling, blasting, transporting, loading, and
unloading frequently result in the production of dust. Other non-point anthropogenic sources of dust
include welding, painting, vehicle maintenance, etc.
6. Compounds emitted during volcanic activity:- such as black smoke, ash, and metals. Release of SO 2,
CO 2, and methane from wetlands, sanitary landfills, and permafrost locations in the northern
hemisphere Dust storms caused by forest and bush fires, land use changes, and the production of
isoprenes and terpenes by forests (precursors to low-level ozone) in the sea as well as forest fires.
Air Circulation Maintenance Industry :
HAVC SYSTEM:-(Heat,ventilation and air condition)
• Heating, ventilation, and air conditioning (HVAC) are essential for producing pharmaceutical items of
high quality.
The operators will also enjoy comfortable surroundings thanks to a well-designed HVAC system.
2. The majority of WHO recommendations are made for systems for solid dosage forms .This may help to
provide a comparison between the criteria for solid dosage form plants and other systems. The
recommendations also make reference to other systems or components that are not relevant to solid
dosage form plants.
• Airlock placements, entrances, and lobby layouts are affected by HVAC system design.
• Room pressure, differential cascades, and cross-contamination management are impacted by
architectural elements.
• Contamination and cross-contamination prevention are crucial design factors.
•At the concept design stage, the HVAC system design should be taken into account.
• The environment's temperature, relative humidity, and ventilation must be suitable.
• The aforementioned shouldn't have a negative impact on the manufacturing and storage of
pharmaceutical items, or on the precise operation of machinery.
The WHO recommendations concentrate on HVAC system design, installation, qualification, and
maintenance.
PRELIMINARY HAZARD ANALYSIS(PHA):-
A semi-quantitative technique known as preliminary hazard analysis is used to: -Identify all potential
dangers and accidental occurrences that may cause an accident.
• Determine the severity of the discovered accidental occurrences.
• Determine the necessary hazard controls and follow-up procedures.
PURPOSE|USE OF PHA:-
1. As a preliminary risk study at the beginning of a project (such as a new plant). Accidents are
primarily brought on by energy releases. The PHA identifies potential energy losses, potential
accidental events, and provides a general assessment of the seriousness of each potential
disaster.
The PHA findings are used to: -
• Compare risk ideas;
• Concentrate on key risk issues
2. As the first stage of a thorough risk study of a proposed system or an existing system.
The PHA's goal is to then identify those unintentional incidents that require a deeper and more
thorough risk study.
3.As a thorough risk analysis of a very straight forward system.
3. The complexity of the system and the analysis's goals will determine whether or not a PHA is
sufficient.
4. Used in a process plant's conceptual design or R&D stage.
5. Often employed as a technique for design assessment before a process is created .
The complexity of the system and the analysis's goals will determine whether or not a PHA is
sufficient.
BENEFITS OF PHS:
1. The finished product must be "safe." A PHA aids designers in recognising and addressing
dangers.
2. Changes made earlier in the design process are less expensive and simpler to implement
than those made later in the process.
3. Aids in hazard anticipation, which lowers the likelihood of surprises throughout the design
phase
PHA SCOPE:-
The PHA must take into account of the following:-
• Dangerous plant equipment and materials (fuels, highly reactive chemical, toxic substances, explosive,
high pressure system, etc.).
• Interfaces between plant equipment components and materials that are safety-related (material
interactions, the start-up and spread of fires and explosions, and control and shutdown systems).
• The environment (earthquake, vibration, flooding, extremely high or low temperatures, electrostatic
discharge, and humidity).
• The use of built-in tests, diagnostics, and emergency procedures; and operation and maintenance.
• Infrastructure support (storage, testing equipment, training utilities).
• Safety-related equipment, such as fire suppression systems, mitigation systems, and personal
protective equipment
• The use of built-in tests, diagnostics, and emergency procedures; and operation and maintenance.
• Infrastructure support (storage, testing equipment, training utilities).
• Safety-related equipment, such as fire suppression systems, mitigation systems, and personal
protective equipment.
FIRE PREVENTION SYSTEM:-
4. Several fire departments do the task of fire prevention. The purpose of fire prevention is to inform the
public about the steps they can take to avoid potentially dangerous fires and to prepare them for how to
survive one. It is a preventative strategy for minimizing emergencies and the harm they cause.
FIRE PREVENTION TRIANGLE:-HEAT, OXYGEN AND FUEL
Heat, oxygen, and fuel are the three ingredients required for a fire. A fire cannot begin or spread if it
lacks heat, oxygen, and fuel. Removing heat, oxygen, or fuel is an important fire prevention tactic. For
the risk of a fire starting or spreading to be as low as possible, the risk assessment should go into detail
on each of the three components.
A detailed and thorough analysis of all the issues, including those related to heat, oxygen, and fuel,
should be included in a fire prevention strategy and a fire risk assessment.
ADVICE ON THIS THREE ELEMENTS IS FOLLOW:-
1.Heat: -is a byproduct of labor operations and is necessary for some processes, including cooking. Heat
must be managed and kept away from fuel unless it is carefully managed. The management of heat
produced as a byproduct of a process is crucial.
Protections: Verify that alt-worship equipment is resistant to catching fire or overheating.
Employ a structured maintenance programme to keep your plant and machinery in good working order.
Evaluate your programme for reporting dangers if you already have one.
• Ensure that staff members understand their obligations.
• Limit ignition sources.
• Schedule regular inspections and cleanings of chimneys.
• Consider distinct building uses, such an office above a shop, as separate purpose groups and keep
them apart from one another.
• Ensure that preparation is continuously watched food .
2.OXYGEN :-
Oxygen gas is used,
•in welding, flame cutting and other similar processes
•for helping people with breathing difficulties .
•In hyperbaric chambers as a medical treatment in decompression chambers
•For food preservation and packaging
5. •In steelworks and chemical plants
The main causes of fires and explosions when using oxygen are:
•Oxygen enrichment from leaking equipment.
•Use of material not compatible with oxygen.
•Use of oxygen in equipment not desired for oxygen service.
•Incorrect or careless operation of oxygen equipment.
PREVENTION:-
• Be mindful of the hazards of oxygen; if unsure, ask.
• Avoid oxygen enrichment by checking that all equipment is in good operating order and is leak-tight.
• Verify the ventilation is sufficient.
Always handle oxygen tanks and related equipment sensibly and correctly.
• Always turn the valves on oxygen cylinders slowly. Avoid smoking in areas where oxygen is being used.
• Never replace an item with a part that hasn't been specifically approved for usage with oxygen.
Never use oxygen equipment above the pressure certified by the manufacturer.
•Never use oil or grease to lubricate oxygen equipment.
Never use oxygen in equipment which is not designed for oxygen service.
3. Fuel:- Workplaces with large concentrations of flammable materials on display, in storage, or being
utilised can be more dangerous than those with smaller concentrations. Fuel is made up of flammable
substances when it comes to fire. A substance that easily burns in a typical environment is flammable.
Among flammable substances are flammable liquids (such as gasoline), flammable gases (such as
propane and butane), and flammable solids (e.g., charcoal, paper). To ensure that the right controls are
in place, it is crucial to identify any combustible products in your workplace.
PREVENTION:-
• Check that workers are aware of their obligation to report dangers.
• When it comes to LPG, heed the authority's guidance.
• Do not allow stairways, hallway walls or ceilings, or any type of timber construction.
• Use caution when installing notice boards along escape routes or in exit corridors as any paper on the
board could serve as fuel in the case of a fire.
6. • Follow the code of conduct to stay safe around underground utilities.
• Do a thorough risk analysis and take into account the need for gas detection equipment when the
presence of flammable gas or vapour is a possibility.
• When equipment for gas detection is required, make sure it is installed, maintained, and serviced
properly.
FIRE EXTINGUISHERS:
A fire extinguisher is a device which can be used to control a fire. It can help remove the fire and may
stop it from burning.
TYPES OF FIRE EXTINGUISHERS:-
1. Water based.
2. Dry powder based.
3. Foam based.
4. Wet chemical and water additives based.
5. Carbon dioxide based
1.A water extinguisher: The label on it is Bright red colour. This kind of extinguisher is utilised to put out
fires brought on by a variety of organic materials, including, but not limited to, paper, cardboard, coal,
fabrics, and other materials. It shouldn't be used for flames in the kitchen, fires brought on by flaming
objects or liquid fires, or other types of fires. using water Only class A fires should be put out with water-
based extinguishers. Foam or electrical equipment is required in the majority of premises
2. Dry powder based: Standard dry powder extinguishers are also referred to as ABC extinguishers;
however, these should not be used in enclosed spaces for Class A, Class 1S&B, and Class C fires. 3S It is
simple to breathe in the dry powder in the extinguisher. Moreover, cleaning up the ash after the fire has
been put out is not advised: They can also be applied to electrical equipment fires. Special dry powder
extinguishers are also available; these are often used to put out flames started by combustible metals.
This type of extinguisher's labels are blue.
• It can also be used to put out flames started by flammable gases like acetylene and liquid petroleum
gas as well as flammable liquids like paint and gasoline. This fire extinguisher may also be used to put
out flames involving equipment up to 1000V.
Special dry powder extinguishers exist, however they are normally only applied to combustible metals
like magnesium and titanium.
Cooking oil fires and flames involving electrical equipment over 1000 V shouldn't be extinguished with
this kind of extinguisher.
7. 3. Foam-based extinguishers: These are the most typical class B fire extinguisher types. Yet, because
they are water-based, they can also be used to put out class A fires. The label is cream in hue.
These fire extinguishers can put out fires started by combustible liquids like gasoline and paint as well as
other organic materials like wood, coal, textiles, fabrics, cardboard, and paper. Kitchen fires, fires
involving electrical equipment, and flames started by combustible metals should not be extinguished
using this kind of extinguisher.
Businesses and locations where the building is built of different organic materials or where it is possible
that such organic materials would be present, such as warehouses, residential properties, hospitals,
schools, offices, and/or structures storing flammable liquids, must have foam extinguishers.
4. Wet chemical and water additive: extinguishers are made to be used on class F fires that involve
cooking with fats. Although foam or water extinguishers are more typical, the wet chemical fire
extinguisher can be used to put out small-scale fires. Dry powder puts out fires more smoothly by
creating a barrier between the source of oxygen and the fuel. This kind of extinguisher's basic colour is
yellow. Fires started by numerous organic materials, such as wood, coal, textiles, fabrics ‘cardboard, and
per, can also be put out with wet chemical extinguishers.
• location: This kind of fire extinguisher should be put close to the fire risk's source. In canteens and
commercial kitchens.
5. Carbon dioxide-based: Carbon dioxide extinguishers are often the primary fire extinguisher type given
in computer server rooms and are primarily utilized for electrical fire threats. By sucking up the oxygen a
fire requires to burn, they suffocate them. The label on this kind of extinguisher is black.
Location: Orfaon dioxide sprinklers need to be placed close to the fire risk's source or close to the fire
exits, such as in offices, kitchens, server rooms, and locations with electrical equipment and appliances.
CRITICAL HAZARD MANAGEMENT SYSTEM: -
The objective of successfully implementing an HMS is the systematic management of hazards:
identifying them, assessing risks and selecting suitable control measures. Regular testing and
maintenance of those controls is essential to ensure they remain effective and for compliance.
The hazard management process: The key elements of any HMS must include:
• Identification of all hazards.
• Determining whether the hazard can be eliminated or isolated.
Assessing the remaining hazards to determine whether they are principal hazards or significant hazards.
Developing and introducing Principal Hazard Management Plans (PHMPs) for principal hazards.
Developing and introducing Principal Control Plans (PCPs) for all principal control mechanisms.
8. For remaining hazards, where they cannot be eliminated or isolated, conducting a risk
assessment to minimize the likelihood of the hazard to workers by setting controls. This should include
Standard Operating Procedures (SOPs) and/or Trigger Action Plans (TARPS) where applicable.
Participation of workers in the identification, assessment and control of hazards.
The hazard management system involves these three basic principles:-
1. Identifying the hazard
2. Risk assessment
3. Controlling hazard
1. Identify the hazard: In an underground setting, the following criteria are utilised to determine dangers
and the risks they pose:
a) A team with a variety of experience and knowledge, including the pertinent health and safety
representative, should identify hazards.
To guarantee that all potential hazards are identified and the ensuing risks are confidently and
thoroughly understood, a comprehensive approach must be used with appropriate detail.
The following factors need to be taken into account while identifying hazards:
Any potential modifications to the way work is structured, managed, or performed, including "Design of
workspaces, work processes, materials, plant, and equipment,
Fabrication, installation, commissioning, handling, and material disposal prohibit workspaces,
equipment, and machinery.
• Materials handling, fabrication, installation, commissioning, and disposal prevent workspaces,
machinery, and equipment.
• Buying products and services.
• Contracting and subcontracting for labour, services, and other goods and services, including contract
terms and obligations to and for contractors.
• Plant and equipment inspection, upkeep, testing, repairs, and replacement.
2. Risk assessment: Determining which hoards are significant hoards and identifying and evaluating
hoards. If this is not possible, then significant risks must be removed OL. When the employees are
removed, the following process should be used to determine which of the identified hazards are
significant, whether they can be eliminated or isolated, and if not, the controls that are needed:
a) Identify and evaluate the nature and magnitude of all potential sources of a hazard and its associated
risks;
9. b) assess the risks arising from each hazard using a recognized risk management methodology;
c) the assessment should take into account all pertinent information currently available.
d) To identify the priorities to be assigned to each risk, evaluate the risks by comparing the level of risk
to pre-established standards.
e) Add any assumptions. made about the identification and evaluation of the risks and hazards Events
included.
f) Identify, evaluate, and choose the best controls to adopt to reduce the risk of damage.
3.Controlling: Control for principal hazards must be documented in the HMS in the form of a principal
hazard management plan, or a 'principal control plan'. In assessing hazard and selecting controls to
implement, the reasons for adopting or rejecting those controls must also be documented.
It is advisable that controls for all other types of hazards be documented in a similar manner so that
when they are reviewed the supporting information is readily available. If a control is reviewed in such
circumstances, the HMS must also be reviewed and revised, as necessary.
Control measures often require supporting documentation, procedures, information, training, resources
and testing to make and keep them effective.
While choosing the proper controls, the following factors may need to be taken into account:
• Procedure? Implementing control measures during the design stage, and having access to qualified
personnel to confirm that modifications and designs adhere to specifications. -Procedures for receiving
and purchasing to make sure they follow the rules.
• Permit to work systems for high-risk or unidentified risks; training requirements; and adjustments to
work processes.
Person protection equipment (PPE) is necessary, as is instruction in how to properly use and maintain it.
Supervision to ensure that casks are complete and functional Procedures and instructions are followed.
• Documents pertaining to plant maintenance, repairs, and alterations.