This document provides an overview of the key plant support services required for a pharmaceutical manufacturing facility. It discusses the need for services related to both manufacturing (e.g. security office, fuel storage, scrap yard, toilet facility) and employees (e.g. vehicle parking, canteen, administrative block, sports facilities, residences). For each service, the document outlines design considerations like location, size and key features. It emphasizes that support areas must be separate from production but easily accessible. The document aims to guide planning of ancillary infrastructure required for successful pharmaceutical operations.
This document provides an overview of key plant support services required for a pharmaceutical manufacturing facility. It discusses services related to manufacturing such as security offices, fuel storage, scrap yards, and toilets. It also covers services for employees like vehicle parking, canteens, gardens, administrative blocks, and training centers. The document includes descriptions and considerations for designing each of these important support areas to ensure successful operations.
This document discusses key aspects in designing food processing plants, including plant layout and feasibility studies. It covers:
1) Distinct design considerations for food industries due to seasonal raw materials, stringent hygiene, and social cost-benefit analysis.
2) Components of a feasibility study including market potential, technical requirements, and financial projections.
3) Key factors in plant layout including flow patterns, equipment arrangement to minimize costs, and secondary considerations like climate and waste disposal.
This document discusses the layout and design of buildings and equipment for parenteral manufacturing facilities. It covers various topics like plant layout, types of layout, area planning with different zones of environmental control, design of filling areas, wall and floor treatments, classification of clean rooms, air flow patterns, and types of equipment used. The key aspects addressed are maintaining aseptic conditions, minimizing contamination, and ensuring smooth material flow.
Industrial management
M.Phamacy
PRODUCTION MANAGEMENT
PRODUCTION CONTROL
PLANNING CONTROL
MATERIAL MANAGEMENT
INVENTORY MANAGEMENT
SALES FORECASTING
BUDGET & COST CONTROL
INDUSTRIAL AND PERSONAL RELATIONSHIP
CONCEPT OF TOTAL QUALITY MANAGEMENT
This document discusses plant layout for pharmaceutical manufacturing. It describes the objectives of plant layout being to integrate machinery, materials, and personnel for efficient production. The main types of layouts are process/functional and product/straight line. Key factors that influence layout include the type of process, space available, operational convenience, and health/safety considerations. Special provisions for pharmaceutical plants include preventing mixing of substances and permitting hygienic production. Storage areas for raw materials and finished goods are also discussed.
The document discusses the bakery industry. It covers topics like the types of bakeries, factors to consider for location selection, food plant layout design, labor facilities, production methods, safety, maintenance, waste management, modernization, and transportation. The key points are that the bakery industry has grown due to changing consumption patterns and westernization. Location selection requires consideration of marketing, infrastructure, and labor. Production involves processes like mixing, proving, baking and cooling. Safety risks include machinery, burns, and hazardous substances. Wastewater treatment may involve pretreatment, screening, and coagulation-flocculation. Modernization and transportation help improve quality and connect producers to consumers.
Prepared by
Er. B. SREENIVASULA REDDY
Assistant Professor (Food Engineering)
College of Food Science and Technology
Chinnarangapuram, Pulivendula – 516390
YSR (KADAPA) District, Andhra Pradesh
Premises - Part of Good Manufacturing PracticesTeny Thomas
This document discusses good manufacturing practices for pharmaceutical premises. It covers factors to consider for location, design, construction, sanitation, maintenance, utilities, and environmental control of premises to prevent contamination. The premises must have defined areas for receiving, sampling, storage, production, packaging, and quality control. Cleaning procedures and environmental monitoring programs are important to control contamination. Grade A or B areas for sterile products require additional controls like air quality standards and maintenance of sterile conditions.
This document provides an overview of key plant support services required for a pharmaceutical manufacturing facility. It discusses services related to manufacturing such as security offices, fuel storage, scrap yards, and toilets. It also covers services for employees like vehicle parking, canteens, gardens, administrative blocks, and training centers. The document includes descriptions and considerations for designing each of these important support areas to ensure successful operations.
This document discusses key aspects in designing food processing plants, including plant layout and feasibility studies. It covers:
1) Distinct design considerations for food industries due to seasonal raw materials, stringent hygiene, and social cost-benefit analysis.
2) Components of a feasibility study including market potential, technical requirements, and financial projections.
3) Key factors in plant layout including flow patterns, equipment arrangement to minimize costs, and secondary considerations like climate and waste disposal.
This document discusses the layout and design of buildings and equipment for parenteral manufacturing facilities. It covers various topics like plant layout, types of layout, area planning with different zones of environmental control, design of filling areas, wall and floor treatments, classification of clean rooms, air flow patterns, and types of equipment used. The key aspects addressed are maintaining aseptic conditions, minimizing contamination, and ensuring smooth material flow.
Industrial management
M.Phamacy
PRODUCTION MANAGEMENT
PRODUCTION CONTROL
PLANNING CONTROL
MATERIAL MANAGEMENT
INVENTORY MANAGEMENT
SALES FORECASTING
BUDGET & COST CONTROL
INDUSTRIAL AND PERSONAL RELATIONSHIP
CONCEPT OF TOTAL QUALITY MANAGEMENT
This document discusses plant layout for pharmaceutical manufacturing. It describes the objectives of plant layout being to integrate machinery, materials, and personnel for efficient production. The main types of layouts are process/functional and product/straight line. Key factors that influence layout include the type of process, space available, operational convenience, and health/safety considerations. Special provisions for pharmaceutical plants include preventing mixing of substances and permitting hygienic production. Storage areas for raw materials and finished goods are also discussed.
The document discusses the bakery industry. It covers topics like the types of bakeries, factors to consider for location selection, food plant layout design, labor facilities, production methods, safety, maintenance, waste management, modernization, and transportation. The key points are that the bakery industry has grown due to changing consumption patterns and westernization. Location selection requires consideration of marketing, infrastructure, and labor. Production involves processes like mixing, proving, baking and cooling. Safety risks include machinery, burns, and hazardous substances. Wastewater treatment may involve pretreatment, screening, and coagulation-flocculation. Modernization and transportation help improve quality and connect producers to consumers.
Prepared by
Er. B. SREENIVASULA REDDY
Assistant Professor (Food Engineering)
College of Food Science and Technology
Chinnarangapuram, Pulivendula – 516390
YSR (KADAPA) District, Andhra Pradesh
Premises - Part of Good Manufacturing PracticesTeny Thomas
This document discusses good manufacturing practices for pharmaceutical premises. It covers factors to consider for location, design, construction, sanitation, maintenance, utilities, and environmental control of premises to prevent contamination. The premises must have defined areas for receiving, sampling, storage, production, packaging, and quality control. Cleaning procedures and environmental monitoring programs are important to control contamination. Grade A or B areas for sterile products require additional controls like air quality standards and maintenance of sterile conditions.
This document discusses cGMP (current good manufacturing practices) regulations enforced by the US FDA. It covers the objectives of cGMP which are to ensure consistent quality and specified standards in manufacturing. It also discusses layout considerations for buildings, services, equipment and maintenance that must meet cGMP requirements. Specifically, it outlines factors for proper plant layout and storage area layout. It details cGMP requirements for lighting, ventilation, plumbing, sanitation and other facility services. It also addresses equipment design, installation, cleaning and maintenance practices.
This document discusses Good Manufacturing Practices (GMP) for sterile pharmaceutical products. It provides an agenda that covers requirements for facilities, equipment, processes, and documentation for sterile manufacturing. Key points include maintaining proper air handling systems with appropriate air classification grades for different areas. Environmental monitoring, garment requirements, sanitation procedures, equipment specifications, and detailed manufacturing and batch documentation standards are also outlined to ensure sterile products are consistently manufactured and controlled to quality standards.
The document provides guidelines for GMP compliance related to premises, buildings, and facilities used for pharmaceutical manufacturing. It addresses requirements for design, construction, and maintenance of premises to minimize risks of contamination and ensure cleaning and maintenance. Specific areas covered include storage, production, quality control, and ancillary facilities. It also provides guidance on air handling, plumbing, lighting, sanitation, and other infrastructure.
This document summarizes the key regulatory requirements for pharmaceutical facilities with reference to cGMP. It begins with an introduction on the regulatory requirements for constructing pharmaceutical plants, which are divided into GMP requirements and factory act rules. It then discusses additional regulations related to pollution, hazardous materials storage, and more. The rest of the document outlines specific cGMP requirements related to areas like surroundings, buildings, water systems, waste disposal, personnel, equipment, raw materials, and more. It provides details on what is required for different departmental areas like storage, production, quality control, and sterile product areas. The document concludes with references.
Feasibility study involves an analysis and evaluation of the design concept from all the relevant angles.
The study provides an immediate indication of the probable success of the enterprise and also shows what additional information is necessary to make a complete evaluation.
It gives an insight in to: requirements of human, financial and material resources; plant and machinery, technology; and economic gains or profitability of the proposed venture.
The document discusses good warehousing practices for pharmaceutical products. It outlines the WHO guidelines which include 6 key areas: 1) personnel requirements to properly staff and train warehouse employees, 2) premises and facility standards regarding storage areas, conditions and security, 3) storage requirements such as documentation, labeling and container standards, 4) handling returned goods with established procedures, 5) dispatch and transportation standards to maintain product quality during delivery, and 6) product recall protocols for defective goods. Following good warehousing practices helps ensure the quality of pharmaceutical products is maintained throughout the storage and distribution process.
InstantGMP Compliance Series - Facility AreasInstantGMP™
This document discusses facility area requirements for cGMP compliant dietary supplement manufacturing. It states that areas should be separated by function, such as receiving, storage, packaging, weighing, and production. Specific areas are then described in more detail, including receiving/shipping, storage, packaging, weighing, production, and ancillary areas. Proper airflow, cleaning, and separation of areas is emphasized to prevent cross-contamination and ensure compliance.
This document provides an overview of Good Manufacturing Practices (GMP) and current GMP (cGMP). It discusses what GMP and cGMP are, the key aspects they cover, the ten principles of GMP, important GMP documents, and Schedule M which outlines GMP requirements for pharmaceutical manufacturing in India. Schedule M includes requirements for factory premises, production areas, warehousing, personnel, sanitation and other key aspects to help ensure quality standards during manufacturing.
This document provides information on current good manufacturing practices (CGMP) regulations enforced by the FDA to ensure quality in pharmaceutical manufacturing. It discusses the importance of CGMP for quality products, customer satisfaction, consistency and company reputation. The objectives are to understand regulatory requirements and minimize risks that can't be detected by final testing. The document outlines various CGMP guidelines related to facilities, equipment, personnel, documentation, batch records, quality control and more. It provides details on specific areas like premises, warehousing, water systems, waste disposal, production areas and equipment cleaning/validation.
This document provides information on the requirements for factory premises for manufacturing homeopathic preparations, cosmetics, and medical devices. It discusses the general requirements for location, buildings, water supply, waste disposal, and staff hygiene. It also outlines the specific plant and equipment needed for producing different types of homeopathic preparations like syrups and ointments, various cosmetic products like powders and creams, and medical devices like perfusion sets, syringes, and their component areas for molding, assembling, storage, washing, drying, sealing, sterilization, and testing.
A detailed study of the organisation and personnel involved in the pharmaceutical industry. These are involved in the guidelines of Good Manufacturing Practices.
The document provides an overview of the history and development of the textile industry in India. It discusses how the first modern cotton textile mill was established in 1818 in Kolkata but failed. The first successful mill was set up in 1854 in Mumbai. The industry expanded rapidly from the 1870s onwards, with 271 mills operating by 1914. After partition in 1947, the industry struggled due to loss of cotton-growing areas but was able to increase domestic production. Today, India is the second largest textile producer and exporter, contributing significantly to GDP and exports. The document also outlines the various processes involved in textile production.
This document outlines Good Manufacturing Practices (GMP) guidelines for drug manufacturing facilities. It addresses requirements for facility premises, materials, production areas, quality control, personnel, and sanitation. Key requirements include preventing contamination risks through proper building/area design, segregation of incompatible operations, control of air handling systems, cleaning procedures, personnel training, and health/hygiene practices. The guidelines are intended to ensure consistent high quality drug production under hygienic conditions.
Facility requirements for Hazardous drug Manufacturingehab mohamed
The document provides guidance for ensuring safety throughout the manufacturing process of hormonal drugs. It emphasizes the importance of personnel safety, environmental safety, and patient safety by following current good manufacturing practice guidelines. This includes minimizing risks of contamination and cross-contamination. The document then lists numerous regulatory and industry standards that should be referred to for sterile drug production.
The document presents a plan for the Mehran Spinning Mill project in Thatta, Pakistan. The proposed 20,000 spindle spinning unit will produce over 54,000 kg of yarn per day for domestic and international markets. Key aspects of the plan include a plant layout, production targets, marketing strategy, organizational structure, infrastructure requirements, and financial projections. The total project cost is estimated at 1.07 billion Pakistani rupees to be funded through promoter equity and bank loans. The internal rate of return is projected to be positive.
This document outlines good manufacturing practices (GMP) for premises, materials, equipment, and documentation used in pharmaceutical manufacturing. It discusses requirements for building location and design, waste disposal, water systems, storage areas, production areas, personnel, and sanitation. Specific guidelines are provided for raw material receipt and storage, manufacturing operations, equipment use and maintenance, and documentation and record keeping. The goal is to ensure proper conditions and controls are in place to prevent mix-ups, contamination, and to allow for efficient production of quality pharmaceutical products.
GMP, Goods manufacturer Practices, Drug and Cosmetic actDrSampuranSuahg
GMP (good manufacturing practices) regulations ensure that pharmaceutical products are consistently manufactured and controlled according to quality standards. Key aspects of GMP include maintaining high standards for facilities, equipment, production processes, packaging and labeling, quality control testing, record keeping, and personnel qualifications. GMP helps to minimize risks of contamination and ensures that products meet specifications for identity, strength, quality, purity and safety.
1. The document discusses Good Manufacturing Practices (GMP) regulations for Schedule M drugs and cosmetics in India.
2. It covers GMP requirements for premises, equipment, sanitation, personnel, production, quality control, documentation and other areas to ensure consistent high quality of pharmaceutical products.
3. Key aspects include requirements for manufacturing facilities, warehouses, equipment calibration, personnel training, hygiene, production supervision, validation of cleaning procedures, and maintenance of records to allow traceability of all manufacturing steps.
This document provides information on food processing plant layout and design. It discusses the objectives of plant layout which include minimizing material handling costs and maximizing space utilization. It also describes different types of layouts like product layout, process layout, and combination layout. Additional topics covered include principles of layout, location factors for industries, facility layout, and specific layouts for different food processing units like potato chips, soft drinks, and instant breakfasts. The document emphasizes hygienic design of facilities along with efficient material and information flow.
The document discusses the design and layout considerations for pharmaceutical manufacturing facilities. It states that premises should be located to minimize risks of cross-contamination from external sources. The interior surfaces should be smooth and allow for easy cleaning. Specific areas for different processes like manufacturing, packaging, laboratories should be separated but laid out in a logical flow. Material and personnel flow should be organized to prevent mix-ups and cross-contamination. Tables and figures provide examples of suitable layouts for manufacturing tablets and liquid oral preparations.
Michel Debes: la gestione del combustibile esaurito e dei rifiuti radioattivi...Forum Nucleare Italiano
Intervento di MIchel Debes ( Head of International Relations, EDF Engineering and Generation Division) al convegno "La gestione dei rifiuti radioattivi" organizzato il 10 Marzo 2011 dal Forum Nucleare Italiano
http://www.forumnucleare.it
This document discusses cGMP (current good manufacturing practices) regulations enforced by the US FDA. It covers the objectives of cGMP which are to ensure consistent quality and specified standards in manufacturing. It also discusses layout considerations for buildings, services, equipment and maintenance that must meet cGMP requirements. Specifically, it outlines factors for proper plant layout and storage area layout. It details cGMP requirements for lighting, ventilation, plumbing, sanitation and other facility services. It also addresses equipment design, installation, cleaning and maintenance practices.
This document discusses Good Manufacturing Practices (GMP) for sterile pharmaceutical products. It provides an agenda that covers requirements for facilities, equipment, processes, and documentation for sterile manufacturing. Key points include maintaining proper air handling systems with appropriate air classification grades for different areas. Environmental monitoring, garment requirements, sanitation procedures, equipment specifications, and detailed manufacturing and batch documentation standards are also outlined to ensure sterile products are consistently manufactured and controlled to quality standards.
The document provides guidelines for GMP compliance related to premises, buildings, and facilities used for pharmaceutical manufacturing. It addresses requirements for design, construction, and maintenance of premises to minimize risks of contamination and ensure cleaning and maintenance. Specific areas covered include storage, production, quality control, and ancillary facilities. It also provides guidance on air handling, plumbing, lighting, sanitation, and other infrastructure.
This document summarizes the key regulatory requirements for pharmaceutical facilities with reference to cGMP. It begins with an introduction on the regulatory requirements for constructing pharmaceutical plants, which are divided into GMP requirements and factory act rules. It then discusses additional regulations related to pollution, hazardous materials storage, and more. The rest of the document outlines specific cGMP requirements related to areas like surroundings, buildings, water systems, waste disposal, personnel, equipment, raw materials, and more. It provides details on what is required for different departmental areas like storage, production, quality control, and sterile product areas. The document concludes with references.
Feasibility study involves an analysis and evaluation of the design concept from all the relevant angles.
The study provides an immediate indication of the probable success of the enterprise and also shows what additional information is necessary to make a complete evaluation.
It gives an insight in to: requirements of human, financial and material resources; plant and machinery, technology; and economic gains or profitability of the proposed venture.
The document discusses good warehousing practices for pharmaceutical products. It outlines the WHO guidelines which include 6 key areas: 1) personnel requirements to properly staff and train warehouse employees, 2) premises and facility standards regarding storage areas, conditions and security, 3) storage requirements such as documentation, labeling and container standards, 4) handling returned goods with established procedures, 5) dispatch and transportation standards to maintain product quality during delivery, and 6) product recall protocols for defective goods. Following good warehousing practices helps ensure the quality of pharmaceutical products is maintained throughout the storage and distribution process.
InstantGMP Compliance Series - Facility AreasInstantGMP™
This document discusses facility area requirements for cGMP compliant dietary supplement manufacturing. It states that areas should be separated by function, such as receiving, storage, packaging, weighing, and production. Specific areas are then described in more detail, including receiving/shipping, storage, packaging, weighing, production, and ancillary areas. Proper airflow, cleaning, and separation of areas is emphasized to prevent cross-contamination and ensure compliance.
This document provides an overview of Good Manufacturing Practices (GMP) and current GMP (cGMP). It discusses what GMP and cGMP are, the key aspects they cover, the ten principles of GMP, important GMP documents, and Schedule M which outlines GMP requirements for pharmaceutical manufacturing in India. Schedule M includes requirements for factory premises, production areas, warehousing, personnel, sanitation and other key aspects to help ensure quality standards during manufacturing.
This document provides information on current good manufacturing practices (CGMP) regulations enforced by the FDA to ensure quality in pharmaceutical manufacturing. It discusses the importance of CGMP for quality products, customer satisfaction, consistency and company reputation. The objectives are to understand regulatory requirements and minimize risks that can't be detected by final testing. The document outlines various CGMP guidelines related to facilities, equipment, personnel, documentation, batch records, quality control and more. It provides details on specific areas like premises, warehousing, water systems, waste disposal, production areas and equipment cleaning/validation.
This document provides information on the requirements for factory premises for manufacturing homeopathic preparations, cosmetics, and medical devices. It discusses the general requirements for location, buildings, water supply, waste disposal, and staff hygiene. It also outlines the specific plant and equipment needed for producing different types of homeopathic preparations like syrups and ointments, various cosmetic products like powders and creams, and medical devices like perfusion sets, syringes, and their component areas for molding, assembling, storage, washing, drying, sealing, sterilization, and testing.
A detailed study of the organisation and personnel involved in the pharmaceutical industry. These are involved in the guidelines of Good Manufacturing Practices.
The document provides an overview of the history and development of the textile industry in India. It discusses how the first modern cotton textile mill was established in 1818 in Kolkata but failed. The first successful mill was set up in 1854 in Mumbai. The industry expanded rapidly from the 1870s onwards, with 271 mills operating by 1914. After partition in 1947, the industry struggled due to loss of cotton-growing areas but was able to increase domestic production. Today, India is the second largest textile producer and exporter, contributing significantly to GDP and exports. The document also outlines the various processes involved in textile production.
This document outlines Good Manufacturing Practices (GMP) guidelines for drug manufacturing facilities. It addresses requirements for facility premises, materials, production areas, quality control, personnel, and sanitation. Key requirements include preventing contamination risks through proper building/area design, segregation of incompatible operations, control of air handling systems, cleaning procedures, personnel training, and health/hygiene practices. The guidelines are intended to ensure consistent high quality drug production under hygienic conditions.
Facility requirements for Hazardous drug Manufacturingehab mohamed
The document provides guidance for ensuring safety throughout the manufacturing process of hormonal drugs. It emphasizes the importance of personnel safety, environmental safety, and patient safety by following current good manufacturing practice guidelines. This includes minimizing risks of contamination and cross-contamination. The document then lists numerous regulatory and industry standards that should be referred to for sterile drug production.
The document presents a plan for the Mehran Spinning Mill project in Thatta, Pakistan. The proposed 20,000 spindle spinning unit will produce over 54,000 kg of yarn per day for domestic and international markets. Key aspects of the plan include a plant layout, production targets, marketing strategy, organizational structure, infrastructure requirements, and financial projections. The total project cost is estimated at 1.07 billion Pakistani rupees to be funded through promoter equity and bank loans. The internal rate of return is projected to be positive.
This document outlines good manufacturing practices (GMP) for premises, materials, equipment, and documentation used in pharmaceutical manufacturing. It discusses requirements for building location and design, waste disposal, water systems, storage areas, production areas, personnel, and sanitation. Specific guidelines are provided for raw material receipt and storage, manufacturing operations, equipment use and maintenance, and documentation and record keeping. The goal is to ensure proper conditions and controls are in place to prevent mix-ups, contamination, and to allow for efficient production of quality pharmaceutical products.
GMP, Goods manufacturer Practices, Drug and Cosmetic actDrSampuranSuahg
GMP (good manufacturing practices) regulations ensure that pharmaceutical products are consistently manufactured and controlled according to quality standards. Key aspects of GMP include maintaining high standards for facilities, equipment, production processes, packaging and labeling, quality control testing, record keeping, and personnel qualifications. GMP helps to minimize risks of contamination and ensures that products meet specifications for identity, strength, quality, purity and safety.
1. The document discusses Good Manufacturing Practices (GMP) regulations for Schedule M drugs and cosmetics in India.
2. It covers GMP requirements for premises, equipment, sanitation, personnel, production, quality control, documentation and other areas to ensure consistent high quality of pharmaceutical products.
3. Key aspects include requirements for manufacturing facilities, warehouses, equipment calibration, personnel training, hygiene, production supervision, validation of cleaning procedures, and maintenance of records to allow traceability of all manufacturing steps.
This document provides information on food processing plant layout and design. It discusses the objectives of plant layout which include minimizing material handling costs and maximizing space utilization. It also describes different types of layouts like product layout, process layout, and combination layout. Additional topics covered include principles of layout, location factors for industries, facility layout, and specific layouts for different food processing units like potato chips, soft drinks, and instant breakfasts. The document emphasizes hygienic design of facilities along with efficient material and information flow.
The document discusses the design and layout considerations for pharmaceutical manufacturing facilities. It states that premises should be located to minimize risks of cross-contamination from external sources. The interior surfaces should be smooth and allow for easy cleaning. Specific areas for different processes like manufacturing, packaging, laboratories should be separated but laid out in a logical flow. Material and personnel flow should be organized to prevent mix-ups and cross-contamination. Tables and figures provide examples of suitable layouts for manufacturing tablets and liquid oral preparations.
Michel Debes: la gestione del combustibile esaurito e dei rifiuti radioattivi...Forum Nucleare Italiano
Intervento di MIchel Debes ( Head of International Relations, EDF Engineering and Generation Division) al convegno "La gestione dei rifiuti radioattivi" organizzato il 10 Marzo 2011 dal Forum Nucleare Italiano
http://www.forumnucleare.it
This document discusses site and plant security at pharmaceutical companies. It outlines the importance of security personnel like a security manager and staff. It describes security measures for entry to the site like perimeter fences, security lights, and armed guards. Entry to plant buildings should have robust doors, good locks, inaccessible windows, and burglar alarms. Internal security involves locking areas, restricting unauthorized access, controlling visitor movement, and searching staff and vehicles. The major current issue is theft during construction projects.
Презентація з дисципліни «Логістика» (для менеджерів). Наведено матеріал «9.2 Фізичний розподіл» (компанії фізичного розподілу, центр консолідації, обліково-договірна одиниця, “палетизація”, “контейнеризація”, «золоті» правила логістики у фізичному розподілі та інше)
Este documento describe una laptop Lenovo Yoga 500-14IHW que tiene una pantalla táctil de 14 pulgadas, un procesador Intel Core i3, 4GB de RAM, 500GB de almacenamiento, y la capacidad de girar la pantalla 360 grados entre los modos portátil, mesa, tienda y tableta. Se ofrece en 24 cuotas de $31.45 o un precio al contado de $642, e incluye características como WiFi, Bluetooth, cámara HD, y puertos USB 3.0 y HDMI.
The document discusses the muscles and joints of the shoulder region. It identifies the major muscles that connect the upper extremity to the scapula, thoracic wall, and shoulder joint. These include the trapezius, deltoid, rotator cuff muscles, and others. It then describes the shoulder joint as a ball-and-socket synovial joint between the humerus and scapula. The joint is stabilized by ligaments and muscles but is also inherently unstable. A wide range of motion is possible at the joint, including flexion, extension, abduction, adduction, and rotation. Blood supply to the region is provided by several arterial anastomoses around the scapula.
The document discusses the 5 most common AdWords fails and how to fix them. The fails are: 1) using broad match keywords without modifiers which can show ads irrelevantly, 2) not using negative keywords which can also show irrelevant ads, 3) not tracking conversions to measure success, 4) not using all available ad extensions to provide more information to users, and 5) not using remarketing to retarget visitors. The document provides tips on how to address each fail such as using modifiers for broad match keywords, implementing negative keywords, setting up conversion tracking, taking advantage of all ad extension types, and following best practices for remarketing ads.
The document discusses factors to consider for plant location and layout planning. For plant location, key factors include availability of raw materials, proximity to markets, labor, transportation, utilities, climate, land, community impact, and environmental regulations. Effective layout planning considers department and workstation arrangement, materials flow, space utilization, supervision, safety, capacity, and future expansion. Common layout types include process, product, group technology, and fixed position layouts, each suited to different production volumes and variety.
Layout of Tablet Manufacturing Section Nitin Kadam
The document discusses the layout and design requirements for a pharmaceutical manufacturing facility. It outlines three main types of layouts - circular flow, parallel flow, and crossover traffic. It emphasizes the importance of proper airflow, temperature control, humidity control, and negative pressure differentials between areas to prevent cross-contamination. It also lists key equipment needed for mixing, granulating, drying, compression, coating, and packaging operations.
The document summarizes key information about fuel cells. It describes that fuel cells directly convert the chemical energy of a fuel, like hydrogen, into electrical energy through electrochemical reactions. It compares the process of fuel cells to ordinary combustion, noting that fuel cells produce electricity and water as products rather than heat. The document then provides details about the components and basic operations of fuel cells, focusing on two commercially important types: phosphoric acid fuel cells and polymer electrolyte membrane fuel cells.
20160923 expocición sobre organigramasElvis U Omar
Este documento presenta información sobre organigramas y diagramas de Gantt. Explica los tipos de organigramas según su naturaleza, finalidad, ámbito, contenido y presentación gráfica. También define el diagrama de Gantt como una herramienta para modelar la planificación de tareas de un proyecto y describe sus pasos de elaboración, ventajas y desventajas. El documento concluye preguntando si hay alguna duda.
Facilities and Location Management
Design of space for Employee Services:
Services related to Employees include
1) Vehicle Parking
2) Canteen and Cooking
3) Garden and Horticulture
4) Administrative Block and Training Centre
5) Sports and Entertainment Block
6) Resident Managers Bungalow
7) Residences for Essential Service Staff
8) Medical Services
The document outlines guidelines for premises and equipment used in the production of traditional medicines and health supplements according to ASEAN standards. It discusses the design, construction, and maintenance of production areas, storage areas, and quality control areas to minimize risks of contamination and permit effective cleaning. Specific requirements for lighting, ventilation, flooring, drainage, and segregated material and personnel flow are provided. The document also addresses changing rooms and storage areas.
Maintainance of Facility & Equipment. pptxThePassenger2
The document discusses key facilities and equipment that require maintenance in the pharmaceutical industry, including HVAC systems, plumbing, drainage, gas systems, and sanitation facilities. It emphasizes that effective maintenance is critical for ensuring product quality and safety, as well as plant reliability and competitiveness. Several specific maintenance best practices are outlined, such as properly training maintenance staff, prioritizing maintenance based on equipment criticality, and implementing total productive maintenance programs.
Sanitary Design An Introduction to Standards of Design Excellence November 2015Bob (Robert L.) Long
This document discusses sanitary design principles for food processing facilities and equipment. It covers several key topics:
- It defines 4 sanitary zones within a facility based on cleanability and risk of contamination.
- It emphasizes that equipment, facilities, and processes must be designed for effective cleaning and maintenance in order to control pathogens. Proper design is important from both food safety and cost perspectives.
- It provides examples of industry standards and guidelines for sanitary design in food processing, including those from 3A Sanitary Standards and EHEDG. Factors like smooth surfaces, drainability, and easy disassembly are important.
- It discusses how to prioritize sanitary risks based on likelihood and impact,
Schedule T: (Schedule T describes the Good Manufacturing Practice for Ayurvedic, Siddha and Unani Medicines.)
The Good Manufacturing Practices (GMP) are prescribed as follows:
Raw materials used in the manufacture of drugs are authentic, of prescribed quality and are free from contamination.
The manufacturing process is as has been prescribed to maintain the standards.
Adequate quality control measures are adopted.
The manufactured drug which is released for sale is of acceptable quality.
"In the food industry, customer experience, food safety, and operational efficiency are of paramount importance. Thus, a well-thought-out site selection and layout design are essential to create a successful and sustainable food-related business.
By following certain process management systems, food industries can significantly minimize the risk of pathogen contamination and uphold the highest food safety standards, ensuring the delivery of safe and wholesome food products to consumers.
Stay at the Cutting Edge of the F&B industry! Discover the Latest Innovations, Trends, and Insights in Our Weekly Newsletter for Food-Tech Enthusiasts."
The document discusses pharmaceutical plant layout and factors that affect layout design. It explains that plant layout refers to the arrangement of machines, equipment, and services within a factory to optimize production processes. Key factors in layout design include the production process, volume, equipment used, and ensuring worker safety. Special provisions are required for sterile and aseptic areas, including controlled airflow and strict access procedures. Proper storage is also important, with raw materials, finished goods, and hazardous materials each requiring dedicated facilities.
THE ROLE OF ENGINEER in Agricultural & FS SectorTandarayen Kevin
The document discusses the role of engineers in the agricultural and food security sector in Mauritius. It outlines that engineers work to meet societal needs through applying scientific knowledge via industry. The engineering division of the Ministry of Agro-Industry and Food Security provides technical support across divisions and undertakes projects related to infrastructure, machinery maintenance, refrigeration, irrigation design and renewable energy. Some challenges faced include ensuring occupational health and safety, sustainable maintenance, and effective training for employees.
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.
Schedule M for Pharmacy Students, Here from Pharmaceutical Jurisprudence 5th Sem.
Make easy in Student language.
Both Pharmacy Students (B Pharm & D Pharmacy
Good Manufacturing Practices (GMP) are a set of guidelines and standards designed to ensure the consistent production and control of high-quality pharmaceutical, food, and medical products. GMPs encompass every aspect of the manufacturing process, from raw materials to finished goods, emphasizing safety, cleanliness, and efficiency. Key elements include proper documentation, employee training, quality management systems, equipment maintenance, and environmental monitoring. By adhering to GMPs, manufacturers can minimize risks, maintain product quality, and ultimately safeguard consumer health.
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Designing of plant support services
1. DESIGNING OF PLANT SUPPORT
SERVICES
Presented by:
Mr. Sonwane S.A
(Roll No: 307)
Under the Guidence of
Mr. Nikam V.K
1
AMRUTVAHINI COLLEGE OF PHARMACY, SANGAMNER
2. CONTENT
Introduction
Plant Support Services
A. Services related to Manufacturing
B. Services related to Employees
Reference
2
3. INTRODUCTION
Definition :- Activity or function required for successful completion of a
process , program or project in the plant is called as plant support services.
Pharmaceutical manufacturing facility required 2 principle areas ;
1) Production Area
2) Support Area
Requirement for the construction of plant :-
1) Requirements related to GMP
2) Requirements related to Factories Act and Rules
3
4. PLANT SUPPORT SERVICES
Plant Support Services includes ;
A. Services related to Manufacturing
B. Services related to Employees
4
5. A. Services related to Manufacturing
1) Security Office
2) Fuel Storage
3) Scrap Yard
4) Toilet Facility
5
6. B. Services related to Employees
1) Vehicle Parking
2) Canteen and Cooking
3) Garden and Horticulture
4) Administrative Block and Training Centre
5) Sports and Entertainment Block
6) Resident Managers Bungalow
7) Residences for Essential Service Staff
8) Medical Services
6
8. SECURITY OFFICE
In every factory 1000 or more workers are ordinarily employed.
Also number of Safety Officers may be specified in factory.
The duties, qualification and conditions of service of Safety
Officers shall be prescribed by the State Government.
Pharmaceutical industry is one of the most diverse fields,
encompassing research, manufacturing, distribution and marketing
with a board range of potential security vulnerabilities.
8
9. Facilities protection requires highest level of security services
related to access control, ingress and egress monitoring, after-
hours protection and alarm monitoring.
Security services required;
1) Access control
2) Fire prevention and life safety programs
3) Demonstration mitigation
4) Facilities protection
5) Crisis management
6) Emergency or unusual event response
9
10. Security offices also required Security Guards working in
private organizations have to keep a tab on people which
entering and leaving the building .
Security guards maintain a book which contains name or in and
out time of the person .
Security guards are responsible for safety of people working in
building .
Security guards also check each and every person before
entering the building .
10
11. DESIGNING OF SECURITY OFFICE
Entry to Factory
11
Locker
Document Room
Alarm
Section
Sitting
Table
Waiting Room
Security Cloth
Room
Toilet
Facility
Exit
from
Factory
Entry Exit
12. DESIGN OF FUEL STORAGE
FACILITY
12
C o m m o n P a s s a g e
Receiving Fire Extinguisher
Intermediate
Liquid Fuel
Storage
Final Liquid
Fuel
Storage
Final Gas Fuel
Storage
Intermediate Gas
Fuel
Storage
Fire Extinguisher
13. FUEL STORAGE FACILITY
Fuel is required in pharmaceutical industries for generating power
during interruption of regular power supply .
Generally Coal, Diesel can be used for this purpose and storage of
these material is necessary.
Canteen required gas for cooking purpose, LPG cylinders are
utilized for the activity.
Care has to be taken while storing these substances.
Storage has to be near the generator room.
Constant check has to be kept on the quantity of the material
stored.
13
14. As these substances are highly inflammable, protection from fire
becomes a basic requirement.
Fire safety equipments are to be in vicinity of such facility and
people are to be trained in handling of the same.
All such fuel are to be stored in a secured area, to avoid tampering
or misuse of these substances.
14
15. SCRAP YARDS FACILITY
During working in the industry, large amount of waste material or
scrap is generated.
This includes the empty cartons in with raw material or packaging
material is plastic sheets, discarded powders, discarded or rejected
products, printed packaging materials, machinery/equipments or
parts of machinery/equipments.
The most common method employed for destruction of these
material is incineration.
Monitoring of particulate matter entering the environment is
critical.
15
16. All materials moved to the scrap yard are to be
documented systematically, record of destruction is also
to be maintained.
Precaution during incineration process are necessary
with respect to the material to be destroyed, fumes
generated, toxic gases evolved.
If material is to be discarded then complete procedure for
metal processing is to be used.
Security measures are also important as any material in
scrap yard should not get stolen.
16
17. DESIGN OF SCRAP YARDS
FACILITY
17
Receiving Area Inspection Room
Disposable
scrap
Nondisposabl
e scrap
Scrap
treatment
Scrap
treatment
18. TOILET FACILITY
Objective :- To provide separate toilet facility for male as well as
female .
The area should be well lighted and ventilated .
Sweepers shall be employed to clean latrines, urinals and washing
places .
Facilities for washing shall be provided and maintained for the use
of the male and female workers separately.
Facilities for changing, storing clothes and for washing and toilet
purposes shall be easily accessible and adequate for the number of
users.
18
19. These area shall not be directly connected with production or
storage areas.
There shall be a written instruction for cleaning and
disinfection of these area.
A routine sanitation program shall be drawn up , observed and
properly recorded.
It indicate that :-
1) Specific areas to be cleaned and cleaning intervals.
2) Cleaning procedure to be followed including equipment and
materials to be used for cleaning.
3) Personnel assigned to and responsible for the cleaning
operation.
19
21. VEHICLE PARKING
Parking design is result of various policies and programs which
result in more efficient use of parking resources.
Parking is an essential component of the transportation system.
Parking area is generally located at the periphery of the premises.
Separate area provided for parking vehicles of the employee’s and
the visitors.
Separate are allocated for parking of 2 wheelers and 4 wheelers.
Allottment of parking area depends on industry’s size, scope and
operations.
21
23. Parking Management Benefits :-
1) Facility Cost Saving
2) Improved Quality of Service
3) More Flexible Facility Location and Design
4) Reduces Land Consumption
5) Supports Mobility Management
6) Supports Smart Growth
7) Improved Walkability
8) More Livable Communities
23
24. Criteria for Design of Parking :-
1) Parking Facility for Personnel Vehicle
2) Parking Facility for Commercial Vehicle
Parameters in Design of Vehicle Parking :-
1) No of Personnel
2) Public Transport Services
3) Distance of Factory from City
4) Private Transports Facilities
5) Feasible Land for Design of Vehicle Parking
6) Environment Condition
7) Vehicle Dimension in Parking Design
24
25. DESIGN OF VEHICLE PARKING
Personnel Vehicle
25
Vehicle Parking
Commercial Vehicle
VIP Staff
Other Staff
Workers
Cars
4 Whealer Parking 2 Whealer Parking
Heavy Vehicle
Cars
Cars
26. 26
TYPE I (a) TYPE I (b) TYPE I (c)
TYPE II TYPE III
27. GARDEN AND HORTICULTURE
Horticulture is the industry and science of plant cultivation
including the process of preparing soil for the planting of seeds,
tubers or cutting.
In industry, gardens are maintained surrounding the facility.
Trees are planted at proximity of the facility.
Clarified water from effluent treatment can be used for watering
the gardens.
27
28. CANTEEN AND COOKING
A. Canteen :-
These area shall not lead directly to the manufacturing and storage
areas .
Canteen usually located at the periphery of the industry .
It is included in the ancillary area of the company .
Area of canteen will depend on the number of workers employed .
The canteen furniture will be in accordance to GMP .
Food may be provided by company which will lead to maintaining
a hygienic cooking facility in canteen .
Employees can have their food in the canteen .
Proper safety equipments are to be kept in place.
28
29. B. Cooking :-
Cooking area has to be maintained under total hygienic condition .
People involved in preparation, serving, cleaning of area are to be
well trained in each activity like personal hygiene practices,
washing of utensils, cleaning of food materials.
Personnel working in canteen have to undergo periodic medical
examination.
These personnel are vaccinated for Typhoid periodically.
Sanitation is the general problem associated with canteen facility.
Presence of food creates a potential rodent and insect problem.
29
30. DESIGN OF CANTEEN FACILITY30
Cooking
place
Grain
storage
Wash
area
Cooked
food
storage
Service
counter
area
Hand
wash
34 M
13 M
31. ADMINISTRATIVE BLOCK AND
TRAINING CENTRE
A. Administrative Block :-
Administrative block involves cabin of HOD .
Conference rooms having a capacity of 4 people and 8 people .
Meeting room having capacity of 20 people. There should be
small library. There should be room for tea making and crockery
storage.
Relative location of the administrative area is of importance.
31
33. DESCRIPTION OF ADMINISTRATIVE
BLOCK
Sr. No. Room Name Dimension
(m)
Description
1 Conference Room 4 x 4 4 Peoples
2 Office – 2 3 x 3 Production Head
3 Office –3 3 x 3 Q. A. Head
4 Office - 4 3 x 3 P.A. of loacation
Head
5 Office – 5 4 x 4 Location Head
6 Wash Room-M 7.6 x 4 -
7 Conference Room 12 x 4.5 20 Peoples
8 Office - 8 3 x 3 Engg. Head
33
34. Sr. No. Room Name Dimension(m) Description
9 Office - 9 3 x 3 Q. C. Head
10 Office - 10 3 x 3 Personnel Head
11 Tea Making &
Crockery Storage
3 x 2.5 -
12 Wash Room - F 5 x 4 -
13 Conference Room 6 x 4 8 Peoples
14 Library 8.54 x 4.5 -
15 Office - 15 3 x 3 Finance &
Factory
Administration
16 Office - 16 3 x 3 Prod. Planning &
Control Head
17 Clark Office - 17 6 x 6 -
34
35. B. Training Centre :-
It is the area where training sessions for employees can be
arranged.
Its location is in the administrative block.
It should contain Projector, T. V, White board.
Sitting arrangement of 25 people or it is also depend on capacity
of plant.
Training varies according to the activity of personnel which
carries out in the industry.
35
36. Design Aspects :-
1) Sitting arrangement for a maximum of 30 persons
(30sq.m) .
2) Trainees table and chair (4 x 2 m)
3) White board (2 x 1.5 m)
4) Projection screen (2 x 1.5 m)
5) LCD projector for slide show
6) Flip charts and mounting stand
7) Disposables
8) Speaker phone / TV set with DVD
9) Training manager office
10) Washroom facility
36
37. DESIGN OF TRAINING HALL37
Library
Training
Manager
office
rReception
Wash
room
White board
Table
Speaker
30 chairs
12.50 M
11 M
Lobby
38. RESIDENCE FOR ESSENTIAL
SERVICE STAFF
Essential Services means services that are necessary to enable the
employer to prevent;
1) Danger to life, health or safety.
2) The destruction or serious deterioration of machinery, equipment
or premises.
3) Serious environmental damage.
4) Disruption of the administration of the courts or of legislative
drafting.
38
39. Essential Services Employee means an employees who is required
to work during a work stoppage.
The residences for these employees have to be in vicinity of the
industry.
As they will be required for the said job at any point of time, either
there will be people working in shifts or in vicinity.
So that problems can be resolved immediately without any loss of
time and money in the company.
39
40. SPORTS AND ENTERTAINMENT
BLOCK
Company can have recreation activity facility in their premises .
Employees can use these facilities after their working hours .
Large scale plants depends on company policy of indoor sports
facility .
Facilities can be for sports, gym, etc .
A common area can be utilized for the purpose like gatherings or
meets of the industry .
Generally table tennis and carom board are placed in these area .
40
41. There is a separate room for study to this wash room is attach .
There should be facility for drinking water .
Common toilet should be attached to study room .
41
42. DESIGN OF SPORTS AND
ENTERTAINMENT BLOCK
42
Coridor
Table Tennis
Carom
12 M
14 M
10 M
Study Room
43. DESCRIPTION OF SPORTS &
ENTERTAINMENT BLOCK
Sr. No. Room Name Description Dimension
(m)
1 Table Tennis Room Arrangement for 2
table tennis board
4.44 x 6.8
2 Carom Board Room Arrangement for 2
carom board
4.44 x 3.2
3 Study Room Seating arrangement
for 20 people 5.52 x 5
4 Wash Room - 5.46 x 2.70
43
44. RESIDENT MANAGERS BUNGALOW
Objective :- To provide residence facility for essential staff within
premises.
These area shall not lead directly to the manufacturing and storage
areas.
Bungalows are to be located at the periphery of the industry. These
can be utilized by the managers who have either come from
corporate or other site of company on official duty.
Bungalows ;
Resident Managers Bungalow (about 150 m2)
Staff Quarters (about 75 m2/flats) – 4 block
Workers (about 50 m2/flats) – 6-8 flats
44
45. DESIGN OF RESIDENCE MANAGER’S
BUNGALOW45
Car
Parking
Residence Manager’s
Bungalow
12.5 M
12.5M
15 M
20 M
46. MEDICAL SERVICES
State Government may appoint qualified medical practitioners to be certifying
surgeons .
Duties of Surgeons:-
1) The examination and certification of young persons .
2) The examination of persons engaged in factories in such dangerous
occupations or processes .
3) Supervising the factories .
46
47. Prior to employment, all personnel, shall undergo medical
examination including eye examination.
Also shall be free from Tuberculosis, Skin and other
communicable or contagious diseases.
They should be medically examined periodically at least once a
year.
All records shall be maintained.
The licensee shall provide the services of qualified physician for
assessing the health status of personnel involved in different
activities.
47
48. REFERENCE
1) Manohar A. Potdar, Pharmaceutical Facilities, Pharma Med
Press, Pg No: 241-258.
48