Swati Spentose Pvt. Ltd. is a manufacturer of APIs located in Vapi, Gujarat, India. The company was established in 1952 as Euresian Chemicals & Equipment and began API manufacturing in 1970 under the leadership of Late Chairman Shri Narayan Jajodia. The factory is located on a 58,168 square foot site and produces non-sterile APIs and intermediates. The company has an effluent treatment plant that treats wastewater to below GPCB and CPCB discharge limits before sending it to the local CETP. Safety, health, and environmental policies and procedures are in place to manage hazardous waste, monitor emissions, and protect personnel and the environment at the facility
A Review on Step-by-Step Analytical Method Validationiosrphr_editor
When analytical method is utilized to generate results about the characteristics of drug related samples it is essential that the results are trustworthy. They may be utilized as the basis for decisions relating to administering the drug to patients. Analytical method validation required during drug development and manufacturing and these analytical methods are fit for their intended purpose. To comply with the requirements of GMP pharmaceutical industries should have an overall validation policy which documents how validation will be performed. The purpose of this validation is to show that processes involved in the development and manufacture of drug, production and analytical testing can be performed in an effective and reproducible manner. This review article provides guidance on how to perform validation characteristics for the analytical method which are utilized in pharmaceutical analysis.
This document discusses cleaning validation, which provides documented evidence that approved cleaning procedures will produce equipment suitable for processing pharmaceutical products. It defines different levels of cleaning validation based on risk. Key aspects covered include cleaning techniques, establishing acceptance criteria, sampling methods, analytical methods, and documentation requirements. The goal of cleaning validation is to achieve an appropriate level of cleanliness to avoid contamination between product batches.
General Principles of Analytical Method of Validation.pdfTamannaKumari8
Validation is the process of establishing documentary evidence demonstrating that a procedure, process, activity carried out in
testing and then production maintain the desirable level of compliance all stages.
The process of providing the analytical procedure is acceptable or its intended us.(ICH Q
Analytical Method Development by High Performance Liquid Chromatographyijtsrd
HPLC is the dominant separation technique in modern pharmaceutical and biomedical analysis because it results in highly efficient separations and in most cases provides high detection sensitivity. Most of the drugs in multi component dosage forms can be analyzed by HPLC method because of the several advantages like rapidity, specificity, accuracy, precision and ease of automation in this method. HPLC methods development and validation plays an important role in new discovery, development, manufacture of pharmaceutical drugs and various other studies related to humans and animals. This review gives information regarding various stages involved in development and validation of HPLC method. Validation of HPLC method as per ICH Guidelines covers all the performance characteristics of validation, like Accuracy, Precision, Specificity, Linearity, Range and Limit of detection, Limit of quantification, Robustness and system suitability testing. Tanmayi Kalamkar | Tejaswini Kande | Naziya Sayyad | Dipti Patil "Analytical Method Development by High Performance Liquid Chromatography" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-6 | Issue-4 , June 2022, URL: https://www.ijtsrd.com/papers/ijtsrd50177.pdf Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/50177/analytical-method-development-by-high-performance-liquid-chromatography/tanmayi-kalamkar
This document discusses the qualification of UV-visible spectrophotometry. It begins by defining qualification as an act or process to ensure something complies with conditions, standards, or requirements. There are four types of qualification: design, installation, operational, and performance. UV-visible spectroscopy is concerned with the ultraviolet and visible regions ranging from 200-780 nm. The document outlines parameters for acceptance procedures and performance qualification of a UV-visible spectrophotometer, including wavelength accuracy, stray light, resolution power, noise, baseline flatness, stability, photometric accuracy, and linearity.
This document discusses manufacturing and dosage control in the pharmaceutical industry. It appears to be lecture notes or course material for an M.Pharm student in the first semester studying quality assurance. The document focuses on producing pharmaceutical dosage forms while maintaining proper dosage levels and consistency in manufacturing.
A Review on Step-by-Step Analytical Method Validationiosrphr_editor
When analytical method is utilized to generate results about the characteristics of drug related samples it is essential that the results are trustworthy. They may be utilized as the basis for decisions relating to administering the drug to patients. Analytical method validation required during drug development and manufacturing and these analytical methods are fit for their intended purpose. To comply with the requirements of GMP pharmaceutical industries should have an overall validation policy which documents how validation will be performed. The purpose of this validation is to show that processes involved in the development and manufacture of drug, production and analytical testing can be performed in an effective and reproducible manner. This review article provides guidance on how to perform validation characteristics for the analytical method which are utilized in pharmaceutical analysis.
This document discusses cleaning validation, which provides documented evidence that approved cleaning procedures will produce equipment suitable for processing pharmaceutical products. It defines different levels of cleaning validation based on risk. Key aspects covered include cleaning techniques, establishing acceptance criteria, sampling methods, analytical methods, and documentation requirements. The goal of cleaning validation is to achieve an appropriate level of cleanliness to avoid contamination between product batches.
General Principles of Analytical Method of Validation.pdfTamannaKumari8
Validation is the process of establishing documentary evidence demonstrating that a procedure, process, activity carried out in
testing and then production maintain the desirable level of compliance all stages.
The process of providing the analytical procedure is acceptable or its intended us.(ICH Q
Analytical Method Development by High Performance Liquid Chromatographyijtsrd
HPLC is the dominant separation technique in modern pharmaceutical and biomedical analysis because it results in highly efficient separations and in most cases provides high detection sensitivity. Most of the drugs in multi component dosage forms can be analyzed by HPLC method because of the several advantages like rapidity, specificity, accuracy, precision and ease of automation in this method. HPLC methods development and validation plays an important role in new discovery, development, manufacture of pharmaceutical drugs and various other studies related to humans and animals. This review gives information regarding various stages involved in development and validation of HPLC method. Validation of HPLC method as per ICH Guidelines covers all the performance characteristics of validation, like Accuracy, Precision, Specificity, Linearity, Range and Limit of detection, Limit of quantification, Robustness and system suitability testing. Tanmayi Kalamkar | Tejaswini Kande | Naziya Sayyad | Dipti Patil "Analytical Method Development by High Performance Liquid Chromatography" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-6 | Issue-4 , June 2022, URL: https://www.ijtsrd.com/papers/ijtsrd50177.pdf Paper URL: https://www.ijtsrd.com/pharmacy/analytical-chemistry/50177/analytical-method-development-by-high-performance-liquid-chromatography/tanmayi-kalamkar
This document discusses the qualification of UV-visible spectrophotometry. It begins by defining qualification as an act or process to ensure something complies with conditions, standards, or requirements. There are four types of qualification: design, installation, operational, and performance. UV-visible spectroscopy is concerned with the ultraviolet and visible regions ranging from 200-780 nm. The document outlines parameters for acceptance procedures and performance qualification of a UV-visible spectrophotometer, including wavelength accuracy, stray light, resolution power, noise, baseline flatness, stability, photometric accuracy, and linearity.
This document discusses manufacturing and dosage control in the pharmaceutical industry. It appears to be lecture notes or course material for an M.Pharm student in the first semester studying quality assurance. The document focuses on producing pharmaceutical dosage forms while maintaining proper dosage levels and consistency in manufacturing.
Sterility Testing is defined as a testing which confirms that products are free from the presence of viable microorganisms. Sterility testing is very important for medical devices, pharmaceuticals, preparations, tissue materials and other materials that claim to be sterile or free from viable microorganisms.
ICH is an international organization that brings together regulatory authorities and pharmaceutical companies from Europe, Japan and the US to discuss guidelines for drug approval. The purpose is to harmonize technical requirements to reduce redundant testing and delays in approval processes while maintaining standards of quality, safety and efficacy. Stability testing provides evidence of how a drug's quality changes over time under different environmental conditions like temperature and humidity to establish appropriate storage conditions and shelf life. [/SUMMARY]
Quality Assurance and Quality Control (MQA 103T)SAVITHA S
This document provides a summary of in-process quality control (IPQC) tests for various semisolid dosage forms including ointments, suppositories, and creams. It describes tests to evaluate properties such as content uniformity, penetration, rate of release, absorption, irritancy for ointments. For suppositories, it outlines tests for appearance, uniformity of weight, melting range, liquefaction time, breaking strength, and dissolution. For creams, rheology and sensitivity testing are discussed. The purpose of these IPQC tests is to ensure quality and performance of semisolid dosage forms during manufacturing.
NABL provides accreditation to laboratories in India based on international standards like ISO 15189 and ISO 17025. It ensures laboratories are properly qualified and provides benefits like increased confidence in test reports and worldwide acceptance. The accreditation process involves an application, document review, assessment of the laboratory's management system and technical competence, and surveillance after accreditation is granted. If qualified, NABL issues an accreditation certificate valid for two years.
The presentation describes types advantages, disadvantages of parenteral preparations, route of administration, general requirement, evaluation, labeling & packaging, containers & their types etc
WHAT IS PHARMACOPOEIA?
HISTORY OF PHARMACOPOEIA
CONTENT OF PHARMACOPOEIA
WHAT IS MONOGRAPH?
PURPOSE OF MONOGRAPH
TYPES OF MONOGRAPH
IMPORTANCE OF CONTENT OF MONOGRAPH
MONOGRAPH DEVELOPMENT PROCESS
INDIAN PHARMACOPOEIA
format of monograph
AYURVEDIC PHARMACOPOEIA
format of monograph
UNNANI PHARMACOPOEIA
format of monograph
SIDDHA PHARMACOPOEIA
format of monograph
GERMAN HOMOEPATHIC PHARMACOPOEIA
format of monograph
US PHARMACOPOEIA
format of monograph
JAPANESE PHARMACOPOEIA
format of monograph
BRITISH PHARMACOPOEIA
format of monograph
EUROPEAN PHARMACOPOEIA
format of monograph
COMPARATIVE STUDY
CONCLUSION
Reference
High Performance Liquid Chromatography (HPLC) is a technique used to separate compounds dissolved in solution using high pressure to push a mobile phase through a column containing a stationary phase. HPLC instruments consist of pumps to deliver the mobile phase, an injector to introduce the sample, a separation column, and detectors. Compounds are separated based on differences in how they partition between the mobile and stationary phases. HPLC provides high resolution separation of complex mixtures and is characterized by its reproducibility, high pressure operation, and ability to use small particle sizes in the column.
This document discusses pharmaceutical packaging materials and quality control testing. It defines primary, secondary, and tertiary packaging. Common packaging materials include glass, plastic, paper, and boards. Quality control tests for glass containers include chemical resistance via powdered glass and water attack tests. Tests are also described for plastic containers, including clarity of extract and non-volatile residue. The document concludes that testing packaging materials is important to ensure the quality, stability, and efficacy of drug products.
Calibration of infrared (IR) spectroscopy ensures the instrument provides accurate measurements. The calibration process involves using a polystyrene film standard to produce an IR spectrum. The spectrum is compared to a reference standard to check if the strongest peak is within 95% of the maximum. If not, adjustments are made to correct the signal. Periodic calibration is needed to account for instrument drift over time and ensure precise results.
The document discusses NABL accreditation, which is provided by the National Accreditation Board for Testing and Calibration Laboratories (NABL) in India. NABL accredits laboratories to ensure they meet technical standards for competence. The accreditation process involves assessments of a laboratory's management system, technical performance, and participation in proficiency testing. Receiving NABL accreditation improves customer confidence and allows access to domestic and international markets by demonstrating a laboratory's technical competence meets international standards.
GMP refers to the integrated management control system and facilities used for manufacturing drugs intended for human use to ensure they are safe and effective. Key aspects of GMP include clearly defined and validated manufacturing processes, trained operators, comprehensive record keeping, quality control, and compliance with regulations. GMP guidelines specify requirements for facilities, equipment, production, packaging, testing, distribution, and quality management.
IPQC and FPQC tests are important quality control steps for creams from raw materials to finished product. Creams are topical semisolid preparations used to deliver drugs to the skin. They can be oil-in-water or water-in-oil emulsions. Evaluation of creams includes tests for physical properties, pH, viscosity, spreadability, irritancy, microbial growth, and preservative efficacy. Creams are packaged in jars or tubes and stored properly to ensure stability.
This document discusses stability studies and drug kinetics. It defines stability as how a product maintains its quality over time. Stability testing is used to determine shelf life, recommended storage conditions, and container suitability. Kinetics deals with the rates of chemical reactions and processes. The order of a reaction determines how concentration influences the reaction rate. Common orders seen in drug degradation are zero order (rate is constant), first order (rate depends on concentration of one reactant), and second order (rate depends on concentrations of two reactants). Understanding reaction kinetics helps predict degradation over time and ensure drug quality.
A brief presentation on the current good manufacturing practices employed in the manufacture of pharmaceuticals in the US.
Comprises of all aspects of good manufacturing practices
This document discusses guidelines for handling Out of Specification (OOS) test results in the pharmaceutical industry. It provides an overview of the history of OOS guidelines, including FDA audits in the 1980s-90s that identified issues like "testing until pass", which led the FDA to publish formal OOS guidelines in 2006. The document outlines the OOS investigation process, which should first thoroughly check for laboratory errors and assign a cause, then may proceed to extended investigations including retesting or plant investigations if no error is found. Tools like 5M analysis and the five whys technique can be used to identify and analyze the root cause.
Contamination control and sterile manufacturingGeorge Wild
Microorganisms like bacteria, viruses, and fungal spores pose a contamination risk in sterile manufacturing. Cleanrooms with strict particle and airflow controls are needed. Personnel procedures aim to minimize shedding of microbes. Sterilization methods like heat aim to achieve a sterility assurance level of 1 in 1 million by killing all microbes or reducing their number below acceptable levels. Key factors in sterilization include the bioburden level and resistance of the most durable microorganism strain present.
The document summarizes the key events and legislation related to pharmaceutical regulation in India. It discusses the origins of pharmacy in India in the early 1900s and the reasons for establishing the Chopra Committee in 1931 to recommend comprehensive drug legislation. The Chopra Committee's recommendations led to the passage of the Drugs Act in 1940. Subsequent legislation included the Pharmacy Act of 1948, Drugs and Magic Remedies Act of 1954, and Narcotic Drugs and Psychotropic Substances Act of 1985. The Hathi Committee was formed in 1975 to analyze the drug industry and recommend measures to improve quality, reduce prices, and ensure drug availability. The Mashelkar Committee was appointed in 2003 to examine drug regulatory issues and suggest improvements
The document discusses pilot plant scale-up techniques. A pilot plant allows examination of a product and process on an intermediate scale before committing to full-scale production. It is important for identifying critical process parameters, producing samples for evaluation, and providing data to determine feasibility of full-scale production. The document outlines general considerations for pilot plant setup and operation including personnel requirements, equipment needs, production rates, process evaluation, and GMP compliance.
This document discusses quality control tests for suppositories. It describes the different types of suppositories and various tests conducted during quality control, including visual examination, uniformity of weight and texture, melting point determination, breaking strength, dissolution testing, content uniformity, and disintegration testing. The goals of these tests are to ensure suppositories meet specifications for attributes like appearance, consistency, and ability to dissolve or disintegrate properly when administered.
The document provides an overview of effluent treatment plants (ETPs) with a focus on requirements for pharmaceutical companies. It discusses what an ETP is, guidelines from WHO GMP and other organizations, why ETPs are necessary, factors to consider in planning one, common treatment methods, and standards in Bangladesh. The presentation aims to educate on proper ETP design and operation to safely treat wastewater before discharge.
Review paper on operation and maintenance of effluent treatment plant of pape...IRJET Journal
This document summarizes a review paper on the operation and maintenance of the effluent treatment plant at a paper industry in India. It describes the company and production processes that generate wastewater effluent. The effluent treatment plant uses a 5-stage process including primary and secondary clarification, aeration, filtration, and chlorination to treat over 22,500 cubic meters of wastewater per day before discharge or reuse. Monitoring shows the treated effluent meets standards for parameters like pH, BOD, COD and TSS. The plant helps minimize environmental impacts and pollution from the industry's operations.
Sterility Testing is defined as a testing which confirms that products are free from the presence of viable microorganisms. Sterility testing is very important for medical devices, pharmaceuticals, preparations, tissue materials and other materials that claim to be sterile or free from viable microorganisms.
ICH is an international organization that brings together regulatory authorities and pharmaceutical companies from Europe, Japan and the US to discuss guidelines for drug approval. The purpose is to harmonize technical requirements to reduce redundant testing and delays in approval processes while maintaining standards of quality, safety and efficacy. Stability testing provides evidence of how a drug's quality changes over time under different environmental conditions like temperature and humidity to establish appropriate storage conditions and shelf life. [/SUMMARY]
Quality Assurance and Quality Control (MQA 103T)SAVITHA S
This document provides a summary of in-process quality control (IPQC) tests for various semisolid dosage forms including ointments, suppositories, and creams. It describes tests to evaluate properties such as content uniformity, penetration, rate of release, absorption, irritancy for ointments. For suppositories, it outlines tests for appearance, uniformity of weight, melting range, liquefaction time, breaking strength, and dissolution. For creams, rheology and sensitivity testing are discussed. The purpose of these IPQC tests is to ensure quality and performance of semisolid dosage forms during manufacturing.
NABL provides accreditation to laboratories in India based on international standards like ISO 15189 and ISO 17025. It ensures laboratories are properly qualified and provides benefits like increased confidence in test reports and worldwide acceptance. The accreditation process involves an application, document review, assessment of the laboratory's management system and technical competence, and surveillance after accreditation is granted. If qualified, NABL issues an accreditation certificate valid for two years.
The presentation describes types advantages, disadvantages of parenteral preparations, route of administration, general requirement, evaluation, labeling & packaging, containers & their types etc
WHAT IS PHARMACOPOEIA?
HISTORY OF PHARMACOPOEIA
CONTENT OF PHARMACOPOEIA
WHAT IS MONOGRAPH?
PURPOSE OF MONOGRAPH
TYPES OF MONOGRAPH
IMPORTANCE OF CONTENT OF MONOGRAPH
MONOGRAPH DEVELOPMENT PROCESS
INDIAN PHARMACOPOEIA
format of monograph
AYURVEDIC PHARMACOPOEIA
format of monograph
UNNANI PHARMACOPOEIA
format of monograph
SIDDHA PHARMACOPOEIA
format of monograph
GERMAN HOMOEPATHIC PHARMACOPOEIA
format of monograph
US PHARMACOPOEIA
format of monograph
JAPANESE PHARMACOPOEIA
format of monograph
BRITISH PHARMACOPOEIA
format of monograph
EUROPEAN PHARMACOPOEIA
format of monograph
COMPARATIVE STUDY
CONCLUSION
Reference
High Performance Liquid Chromatography (HPLC) is a technique used to separate compounds dissolved in solution using high pressure to push a mobile phase through a column containing a stationary phase. HPLC instruments consist of pumps to deliver the mobile phase, an injector to introduce the sample, a separation column, and detectors. Compounds are separated based on differences in how they partition between the mobile and stationary phases. HPLC provides high resolution separation of complex mixtures and is characterized by its reproducibility, high pressure operation, and ability to use small particle sizes in the column.
This document discusses pharmaceutical packaging materials and quality control testing. It defines primary, secondary, and tertiary packaging. Common packaging materials include glass, plastic, paper, and boards. Quality control tests for glass containers include chemical resistance via powdered glass and water attack tests. Tests are also described for plastic containers, including clarity of extract and non-volatile residue. The document concludes that testing packaging materials is important to ensure the quality, stability, and efficacy of drug products.
Calibration of infrared (IR) spectroscopy ensures the instrument provides accurate measurements. The calibration process involves using a polystyrene film standard to produce an IR spectrum. The spectrum is compared to a reference standard to check if the strongest peak is within 95% of the maximum. If not, adjustments are made to correct the signal. Periodic calibration is needed to account for instrument drift over time and ensure precise results.
The document discusses NABL accreditation, which is provided by the National Accreditation Board for Testing and Calibration Laboratories (NABL) in India. NABL accredits laboratories to ensure they meet technical standards for competence. The accreditation process involves assessments of a laboratory's management system, technical performance, and participation in proficiency testing. Receiving NABL accreditation improves customer confidence and allows access to domestic and international markets by demonstrating a laboratory's technical competence meets international standards.
GMP refers to the integrated management control system and facilities used for manufacturing drugs intended for human use to ensure they are safe and effective. Key aspects of GMP include clearly defined and validated manufacturing processes, trained operators, comprehensive record keeping, quality control, and compliance with regulations. GMP guidelines specify requirements for facilities, equipment, production, packaging, testing, distribution, and quality management.
IPQC and FPQC tests are important quality control steps for creams from raw materials to finished product. Creams are topical semisolid preparations used to deliver drugs to the skin. They can be oil-in-water or water-in-oil emulsions. Evaluation of creams includes tests for physical properties, pH, viscosity, spreadability, irritancy, microbial growth, and preservative efficacy. Creams are packaged in jars or tubes and stored properly to ensure stability.
This document discusses stability studies and drug kinetics. It defines stability as how a product maintains its quality over time. Stability testing is used to determine shelf life, recommended storage conditions, and container suitability. Kinetics deals with the rates of chemical reactions and processes. The order of a reaction determines how concentration influences the reaction rate. Common orders seen in drug degradation are zero order (rate is constant), first order (rate depends on concentration of one reactant), and second order (rate depends on concentrations of two reactants). Understanding reaction kinetics helps predict degradation over time and ensure drug quality.
A brief presentation on the current good manufacturing practices employed in the manufacture of pharmaceuticals in the US.
Comprises of all aspects of good manufacturing practices
This document discusses guidelines for handling Out of Specification (OOS) test results in the pharmaceutical industry. It provides an overview of the history of OOS guidelines, including FDA audits in the 1980s-90s that identified issues like "testing until pass", which led the FDA to publish formal OOS guidelines in 2006. The document outlines the OOS investigation process, which should first thoroughly check for laboratory errors and assign a cause, then may proceed to extended investigations including retesting or plant investigations if no error is found. Tools like 5M analysis and the five whys technique can be used to identify and analyze the root cause.
Contamination control and sterile manufacturingGeorge Wild
Microorganisms like bacteria, viruses, and fungal spores pose a contamination risk in sterile manufacturing. Cleanrooms with strict particle and airflow controls are needed. Personnel procedures aim to minimize shedding of microbes. Sterilization methods like heat aim to achieve a sterility assurance level of 1 in 1 million by killing all microbes or reducing their number below acceptable levels. Key factors in sterilization include the bioburden level and resistance of the most durable microorganism strain present.
The document summarizes the key events and legislation related to pharmaceutical regulation in India. It discusses the origins of pharmacy in India in the early 1900s and the reasons for establishing the Chopra Committee in 1931 to recommend comprehensive drug legislation. The Chopra Committee's recommendations led to the passage of the Drugs Act in 1940. Subsequent legislation included the Pharmacy Act of 1948, Drugs and Magic Remedies Act of 1954, and Narcotic Drugs and Psychotropic Substances Act of 1985. The Hathi Committee was formed in 1975 to analyze the drug industry and recommend measures to improve quality, reduce prices, and ensure drug availability. The Mashelkar Committee was appointed in 2003 to examine drug regulatory issues and suggest improvements
The document discusses pilot plant scale-up techniques. A pilot plant allows examination of a product and process on an intermediate scale before committing to full-scale production. It is important for identifying critical process parameters, producing samples for evaluation, and providing data to determine feasibility of full-scale production. The document outlines general considerations for pilot plant setup and operation including personnel requirements, equipment needs, production rates, process evaluation, and GMP compliance.
This document discusses quality control tests for suppositories. It describes the different types of suppositories and various tests conducted during quality control, including visual examination, uniformity of weight and texture, melting point determination, breaking strength, dissolution testing, content uniformity, and disintegration testing. The goals of these tests are to ensure suppositories meet specifications for attributes like appearance, consistency, and ability to dissolve or disintegrate properly when administered.
The document provides an overview of effluent treatment plants (ETPs) with a focus on requirements for pharmaceutical companies. It discusses what an ETP is, guidelines from WHO GMP and other organizations, why ETPs are necessary, factors to consider in planning one, common treatment methods, and standards in Bangladesh. The presentation aims to educate on proper ETP design and operation to safely treat wastewater before discharge.
Review paper on operation and maintenance of effluent treatment plant of pape...IRJET Journal
This document summarizes a review paper on the operation and maintenance of the effluent treatment plant at a paper industry in India. It describes the company and production processes that generate wastewater effluent. The effluent treatment plant uses a 5-stage process including primary and secondary clarification, aeration, filtration, and chlorination to treat over 22,500 cubic meters of wastewater per day before discharge or reuse. Monitoring shows the treated effluent meets standards for parameters like pH, BOD, COD and TSS. The plant helps minimize environmental impacts and pollution from the industry's operations.
Performance Evaluation of Dairy Wastewater Treatment PlantIRJET Journal
1) The document analyzes the performance of a dairy wastewater treatment plant in Jaipur, India.
2) It evaluates various water quality parameters (BOD, COD, TSS, oil/grease) at the plant's inlet and outlet to assess the plant's ability to treat wastewater to regulatory standards.
3) The results show that the plant significantly reduces all parameters measured (BOD reduced from 1477 mg/L to 12 mg/L) and meets regulatory limits for treated water discharge.
This report details an EMS audit conducted at Reliance Industries by DDU and provides exposure to EMS system implementation in the petrochemical industry. The audit assessed parameters like air, water, effluent and waste to ensure compliance with GPCB guidelines. Reliance has implemented an effective EMS based on the PDCA cycle and monitors parameters daily to meet targets and legal requirements. Key aspects of the EMS include an air and effluent monitoring system, landsink ladder for waste management, and a secured landfill site for hazardous waste disposal. The training exposure provided insight into Reliance's EMS procedures and a visit to the effluent treatment plant.
Implementing A Socially Responsible Environmental Management System.pptxJuanCamilo166759
The document discusses the requirements for achieving ISO 14001 certification for environmental management. It outlines the main requirements of the ISO 14001 standard which are scope, leadership, planning, support, operation, performance evaluation, and improvement. The standard requires organizations to identify environmental aspects, impacts, and risks of their activities and put plans in place to reduce negative impacts. It also discusses performing a life cycle assessment according to ISO 14040 which involves defining the goal and scope, inventory analysis, impact assessment, and interpretation phases. Finally, the document provides an example of an agricultural and industrial company conducting an environmental management system analysis of its processes according to the ISO 14001 requirements.
This document provides information about an environmental performance assessment study of the alcohol industry conducted in Uttar Pradesh, India. It lists the study team which included members from the Uttar Pradesh Pollution Control Board and an environmental consultancy. The document outlines the analytical framework used in the study, which evaluated distilleries based on their plant performance, regulatory compliance, and environmental initiatives. It provides details on the evaluation criteria and weightings used to calculate environmental performance ratings for each distillery. Summary statistics and rankings are also given for some of the key plant performance indicators analyzed in the study.
This document provides details on an environmental management plan project conducted in 1999-2000 for the CIB Refinery of ECOPETROL in Colombia. The project developed an environmental impact study and instructions to improve the refinery's environmental performance from 2000-2010. It involved assessing waste management practices and developing recommendations to align them with national and international standards. The author was contracted to build an environmental index to monitor waste disposal management at the refinery.
This document provides information on the production of single superphosphate (SSP) fertilizer. It discusses the raw materials used, including rock phosphate and sulfuric acid. The production process involves acidulation of rock phosphate using sulfuric acid in a den, followed by scrubbing, granulation, drying, and screening. Process flow diagrams and material balances are presented. Equipment used is also described. The document evaluates capital costs, production costs, profitability, and provides a HAZOP analysis for the feeder.
Report on Effluent Treatment Plant (ETP) Operation and Maintenance of Interst...Kowshick Sen
Interstoff Apparels Ltd (IAL) comprises of the latest, most technologically advanced 100% export oriented private limited company with composite knitting, dyeing, finishing and apparel manufacturing plants situated in Chandra, Kaliyakoir, Gazipur, Bangladesh. IAL installed an Effluent Treatment Plant of 75 m3/Hr capacity which is running 24 Hr in a day. By nature, our ETP is Bio-logical with Chemical namely Bio-Chemical plant. This treatment is done by four stages such as preliminary, primary, secondary and tertiary treatment. Waste water comes from mainly dyeing and washing through a trench to equalization tank so for preliminary treatment is done by screening by using net or sieve for removal of large solids such as rags, sticks, grit and grease that may result in damage to equipment or operational problems at different stages of trench.
The Waste Pickling Liquor (WPL) generated in the galvanizing industries is a hazardous waste (Cat.12.2) as per the Hazardous and Other Waste (Management and Transbounary Movement) Rules, 2016 (HW Rules 2016). Hazardous and Other Wastes in the country are required to be managed as per the methods, technologies and Standard Operating Procedures (SOPs) notified by the Govt of India under these Rules. These Rules also provide scope for utilization of the wastes generated from one source in various other applications. The interested users of the hazardous and other wastes are required to obtain permission from the Central Pollution Control Board (CPCB) for this purpose. The grant of permission by CPCB involves conducting of trial runs to study and confirm the environmentally safe use of the intended waste in the proposed activity. In case of the use is found to be environmentally safe, CPCB prepares the SOP for the use and grants permission on a case to case basis. There has not been any application made so far for obtaining such permission for the use of the spent acid that is generated in galvanizing industries. Also, the cheap and easy availability of the hydrochloric Acid (HCl) in the country does not leave much scope for a viable recovery of the virgin HCl from WPL. The galvanizing industries therefore have a limited option of treating the WPL in their premises. The treatment of WPL by lime is an effective and widely practiced method. However, the lime treatment of the WPL leaves a very high concentration of the Total Dissolved Solids (TDS) in the treated waste water. The installation of RO/MEE systems at the industry level does not seem to be viable. Solar evaporation system also requires lot of open to sky area in the industry. The treated effluent with high TDS can be either discharged as such in coastal areas or to be treated at a common facility. However, there is lot of scope for the segregation of the spent HCl and its use in other industries/activities after obtaining the required permission from the CPCB. The segregation of the spent HCl also eliminates the problem of TDS in the waste water resulting from the treatment of the rest of the WPL. The galvanizing industry therefore needs to explore the possible uses of the spent HCl in other industrial activities and obtain permissions from CPCB for such uses instead of allowing to it to become part of the WPL. The presentation gives details of the relevant provisions of the HW Rules 2016, the status of the SOPs prepared so far by the CPCB, the limitations of acid recovery from the WPL and the recommendations for an environmentally sound management of the WPL.
ENVIRONMENT MANAGEMENT IN MINES env_act_1986Jignesh Ruperi
The document summarizes the Environment Protection Act of 1986 in India. It was enacted after the Bhopal gas tragedy to provide a framework for protecting the environment. The key objectives of the act are to implement international agreements on the environment, coordinate regulatory agencies, punish those endangering the environment, and ensure sustainable development. It gives powers to the central government to constitute authorities to enforce standards and restrict pollution. It also outlines penalties for non-compliance. The case study of the Bhopal gas tragedy that prompted the law is also summarized.
This document provides information about an environmental performance assessment study of the alcohol industry conducted in Uttar Pradesh, India. It lists the study team which included members from the Uttar Pradesh Pollution Control Board and an environmental consultancy. The document outlines the analytical framework used in the study, which evaluated distilleries based on their plant performance, regulatory compliance, and environmental initiatives. Various environmental performance criteria were identified and weighted to calculate scores. The results of the study included ratings of distilleries and identification of opportunities for improved environmental performance.
This document provides information about an environmental performance assessment study of the alcohol industry conducted in Uttar Pradesh, India. It lists the study team which included members from the Uttar Pradesh Pollution Control Board and an environmental consultancy. The document outlines the analytical framework used in the study, which evaluated distilleries based on their plant performance, regulatory compliance, and environmental initiatives. It provides details on the environmental performance criteria and weightings used to rate the distilleries in each category. Summary statistics and rankings of the top and bottom performing distilleries are also presented for several plant performance indicators.
This document provides information about an environmental performance assessment study of the alcohol industry conducted in Uttar Pradesh, India. It outlines the study team which coordinated and executed the study. The study developed an analytical framework to evaluate distilleries based on their plant performance, regulatory compliance, and environmental initiatives. Various environmental performance criteria were identified and weighted to calculate scores for distilleries. The document presents some results of the study, including ranges and top/bottom performers for metrics like capacity utilization and molasses consumption. The overall aim was to provide ratings to increase awareness and encourage improvements in environmental performance.
Quick Reference Guide to Relevant Industrial Standards of Sri LankaB.K.T. Samarasiri
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Vishal Shivprasad Purohit is seeking new career opportunities. He has over 15 years of experience in environmental roles, including operating effluent treatment plants, stripper plants, and incinerators. His experience includes roles at Alembic Pharmaceuticals, Alembic Ltd., Tonira Pharma, and Narmada Chematur Petrochemicals, where he managed staff and was responsible for plant operations, compliance reporting, and process optimization. He holds an MSc in Ecology and Environment and is currently a Senior Executive at Alembic Ltd., earning 5 lakhs annually.
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3. 1952 the Group established under the name of Euresian Chemicals &
equipment in Kolkata (trading in steel, chemicals &
pharmaceuticals).
1970 Late chairman Shri Narayan Jajodia, arrived in Mumbai to
specialize the business of the API.
1970 Distribution business within India & across 30 countries.
Extraordinary skills and networks globally in sourcing new
molecules .Representing some of the best pharmaceutical
manufacturers in Europe.
1996 Logical backward integration into manufacturing of bulk
drugs having a strong market position.
Swati Spentose Pvt. Ltd.
History of the Organization
4. General Information
Swati Spentose Pvt. Ltd. Unit – I,
the API Division of Euresian
group, a well – diversified business
group in India is engaged in the
manufacturing and marketing of
non-sterile API/Intermediate.
The Plant is located at Vapi, GIDC,
180 kms from Mumbai, in the
western part of India. Mumbai is
well connected by road, rail and
air. The site is housed in a 5404 M²
area (58,168 ft²) with 4,852 M²
(52,226 ft²) manufacturing &
storage area.
Registered & Corporate Office
Swati Spentose Private Limited
114 Marine Chambers,
11, New Marines Lines,
Mumbai 400 020,
Maharashtra, India
Tel : 91 22 61505222
Fax : 91 22 22071955
Manufacturing Facility
Swati Spentose Private Limited
A-1/2102& 3, Phase III, GIDC
Vapi , 396 195 Gujarat, India
Tel : 91 -260- 2433133
Fax : 91-260-2431572
Swati Spentose Pvt. Ltd.
8. Background of VAPI CETP
CETP was commissioned in 1997. In 2001, All wastewater generated in the estate
were linked to CETP to ensure that environment is protected.
VWEMCL set up a common solid waste management site in 1999 and in year 2000
1st moratorium were imposed in 2009 due to critically polluted area Vapi and lifted
out in 2011
VAPI CETP were designed initially 55 MLD. As on today capacity is 85 MLD
Again moratorium were imposed in sept 2013 due to pollutions and still under
Initially CETP were allowing the discharge permission at 1000 COD and 250 BOD
now GPCB is stagnating the COD 250 and 30 BOD, whereas we are already treating the
effluent on said level
9. WASTE WATER MANAGEMENT
Swati Spentose Pvt. Ltd.
Sr.
No.
Parameters Inlet Quality Outlet Quality Required (for
CETP inlet)
1 pH 7 7
2 COD 15000 <1000
3 BOD 5000 <250
4 SS 320 <100
5 Oil and Grease 75 <10
• Effluent treatment plant installed at SSPL is designed according to the
Pollution Board norms and appreciated by CPCB & GPCB.
• Quantity of wastewater generated from the proposed operation is ~ 41
KL/Day.
• Effluent generated will be treated in Effluent Treatment Plant of 60 KL/Day
capacity.
• ETP Design Parameters
10. Safety and Environment
• Method of treatment shall be as follows:
• Primary Treatment
• Bar Screen - To remove coarse material and grid particles.
• Oil & Grease trap - To remove oil and floatable material.
• Equalization Tank - To maintain the pH of the effluent.
• Clariflocculator / Settling tank - To mix the effluent and remove suspended solids.
• Secondary Treatment (Biological Treatment) – 2 Stage
• Activated sludge process shall be used to convert dissolved organic matter by
microorganism into various gases such as CO2 and into cell tissue, which shall be
removed as sludge.
• Tertiary Treatment
• Pressure sand Filter - To remove residual sludge.
• Activated charcoal filter - To remove odor and color of the effluent.
Swati Spentose Pvt. Ltd.
11. Swati Spentose Pvt. Ltd.
Sr. No. Hazardous
Waste
Category No.
Description of
Hazardous Waste
Quantity
Per Month
Treatment
Disposal
1 5.1 Used oil/spent oil 100 Lit Incarnation or sell
to authorized re-
processor
2 28.1 Residues & waste 1650 Kg To be disposed at
TSDF Vapi3 28.2 Spent Carbon 1170 Kg
4 33.3 Discarded containers 30 Nos. To be
decontaminated &
sold to authorized
re-processors
5 34.4 Chemical sludge &
waste from ETP
4500 Kg Dispose at TSDF
Vapi
6 28.1 Used filter cloth 50 Nos.
Hazardous Waste management
12. ALUM DOSING
LIME DOSING
AIR BLOWER
OIL &
25% REDUCTION IN COD
PRIMARY SETTLING TANK
AERATION TANK-I
EQUALISATION TANKS - 2 NOS.
SECONDARY
INTERMEDIATE
SAND
POLY. DOSING
FLOW: 60m3/day
15000 mg/L COD
TREATED EFFLUENT DISPOSED
BACK WASH TO
COLL. SUMP
SCREEN
FINAL COLLECTION SUMP
TO GIDC U/G DRAINAGE
SYSTEM
TUBE SETTLER
COLLECTION
WATER LEVEL
NEUTRALISATION
AERATION TANK-II
FINAL
G
ACTIVATED
OVERFLOW
SLUDGE RE-CIRCULATION LINE
SLUDGE RE-CIRCULATION LINE
SLUDGE COLLECTION SUMP
G
TO FILTER PRESS
PUMP DIFFUSER SYSTEMAIR BLOWER
F.G.L.
ALKLINE
REACTION TANK
NaOCL DOSING
INLET PIPE
11250 mg/L 70% REDUCTION IN COD
3375 mg/L
80% REDUCTION IN COD
675 mg/L
PUMP
WITH COARSE BUBBLE AERATION
PUMP PUMP
COLLECTION TANK
PRESSURE
FILTER
PUMP
F.G.L.
DIFFUSER SYSTEM
F.G.L.
WATER LEVEL
WATER LEVEL
TUBE SETTLER
WATER LEVEL
TUBE SETTLER
WATER LEVEL
WATER LEVEL
G
W.L.
WATER LEVEL
PUMP WATER LEVEL WATER LEVEL
W.L.
CARBON
FILTER
SETTLING TANK
SUMPGREASE TRAP
CHAMBER
CHLORINATION
TREATMENT
SETTLING TANK
TANKS - 2 NOS.
Swati Spentose Pvt. Ltd.
Schematic Drawing of Effluent Treatment Plant
14. Swati Spentose Pvt. Ltd.
Key highlights and appreciation
According to GPCB vigilance team we are only the industries who have such full-
fledged ETP in VAPI
We are complying CPCB norms 250 COD whereas all VAPI CETP members
discharging the effluent as per CETP inlet norms i.e. 1000 COD
We have the dedicated laboratory for ETP
We follow good document practice in ETP
We have dedicated operation team
15. Swati Spentose Pvt. Ltd.
Background of Kadam Environment project
Kadam Environmental Consultants, Vadodara, Gujarat have been entrusted by Swati Spentose Pvt. Ltd. for carrying out the above mentioned study. Kadam
Environmental Consultants (KEC) is one of the oldest and largest environmental consulting firms in Gujarat and India with about 160 personnel deployed in
various activities.
KEC has been active in this field of environment since 1981 and has carried out several assignments in India as well as abroad. KEC has a full-fledged division
for environmental impact assessment and audits with chemical engineers, environmental planners, environmental engineers, civil engineers, microbiologists,
zoologists, botanists, chemists and industrial chemists (including persons specializing in fieldwork pertaining to sampling).
The company has its own air, water, microbiological and soil laboratories for analyzing physicochemical and bacteriological parameters including heavy metals.
The KEC laboratories are certified to ISO 9001-2000 and are inspected by Gujarat Pollution Control Board(GPCB) as well as the Central Pollution Control Board
(CPCB) Regional Office at Vadodara at regular intervals. The KEC laboratory at Vadodara is recognized by the Ministry of Environment and Forests (MoEF)
under the Environment Protection Act, 1986. KEC is registered as a Consultant with the Gujarat Pollution Control Board and also recognized as Environmental
Auditors (under the Environmental Audit scheme propounded by the Honorable High Court of Gujarat) by the Gujarat Pollution Control Board.
16. Swati Spentose Pvt. Ltd.
S. No. Aspects covered Compliance
1 Mitigative Measures All suggested mitigative measures will be
implemented
2 Environmental Monitoring Ambient, stack & water monitoring will
be done as per CPCB/GPCB guidelines
3 Environmental Management
Cell (EMC)
EMC created with allocated
responsibilities (Director responsible for
environ-mental policy and directions)
Environmental Management Plan
17. Swati Spentose Pvt. Ltd.
Environmental Monitoring Plan
Sr.No. Activity Schedule
Air Pollution Monitoring
1. Ambient air monitoring of parameters specified by GPCB in their air
consents from time to time within the Swati Spentose’s premises
Once every Quarter
1. Ambient air monitoring of parameters specified by GPCB in their air
consents from time to time at four stations outside Swati Spentose
Once every season at each station
1. Stack monitoring of all process / flue stacks sets as given in air consent
from time to time
Once every Quarter for each stack
Water Pollution Monitoring
4. Monitoring of wastewater inlet and outlet at ETP plant for the parameters
specified by GPCB in their water consent from time to time
Daily
5. Monitoring of one sample of ground water at plant / nearby location.
Parameters are essential parameters as per IS: 10500:1991.
Once every season
Solid Waste Generation Monitoring / Record Keeping
6. Records of generation of used drums, bags and records of their dispatch
to suppliers for refilling
Daily
7. Records of generation of waste oils and their treatment Daily
8. Records of generation, handling, storage, transportation and disposal of
other solid, aqueous and organic hazardous wastes as required by
hazardous waste authorization
To be updated daily
Environmental Audit
9. Environmental statement under the EP (Act) 1986 Once in a year
18. Sr. no Head Approximate recurring
cost per annum (Rs. in
lacs)
Approximate Capital
cost (Rs. In Lacs)
1. Air pollution control 0.72 20.5
2. Water pollution control 21.9 100
3. Noise pollution
monitoring
0.12 0
4. Solid and hazardous
waste management
3.36 5.5
5. Environment
monitoring and
management
2 0
6. Green belt 0.80 1.26
Total 28.90 127.26
Swati Spentose Pvt. Ltd.
19. Occupational Health and Safety Policy
Swati Spentose Pvt. Ltd. (SSPL) has a strong commitment to Health, Safety and Environmental (HSE)
performance and a core value of our organization. Good HSE performance in health, safety & security of
everyone who works with SSPL which is a critical asset of our business.
It is the responsibility of every employee to strictly follow SHE practices and create a safe and healthy
environment for self and others. Our goals simply stated are – no accidents, no harm to people & no
damage to the environment.
The objectives of our Health and Safety policy are to:-
• Promote safe behavior amongst those who work with for us, openly report all incidents and encourage
those who work for us to stop work that is unsafe.
• Provide training, education & other relevant information required to facilitate safe working.
• Comply with and abide by all relevant Statutory Provisions pertaining to Health, Safety & Environment in
achieving our business objectives.
• Periodically assess statue of Health and Safety risk in operations through audits and risk assessments and
take corrective action as relevant.
• Benchmark and adopt best practices in Health & Safety & endeavor for continual improvement.
• Integrate Safety & Health in all decisions concerning the operations like purchase of equipment, materials
selection & Placement of personnel.
• Demonstrate visible commitment to Safety and Health across all levels of management, starting from the
top.
Toward meeting the above stated goals in Health & Safety, the company encourages reporting any unsafe
work practices or operations by persons so that corrective and preventive actions can be taken
immediately.
Swati Spentose Pvt. Ltd.
20. Personnel
SSPL Unit – I is committed to Good Manufacturing Practices, Quality Systems and Work
Culture backed by highly committed and skilled manpower, continuous R&D activities, modern
manufacturing facilities and tremendous marketing capabilities. “V” group, with its motto, is
leading ahead to provide health care services to the community at large.
There are an adequate number of personnel qualified by appropriate education, training, and/or
experience to perform and supervise the manufacture .
The responsibilities of all personnel engaged in the manufacture of intermediates and APIs are
specified in writing.
Responsibilities of all personnel are engaged in manufacturing activities is specified and his
acceptance of responsibility is kept in.
Training is regularly conducted by qualified individuals and covers, at a minimum, the particular
operations that the employee performs and GMP as it relates to the employee's functions.
Records of training are maintained.
Swati Spentose Pvt. Ltd.
21. Personal Hygiene
At the time of new appointment, Personnel Department arranges the pre-employment medical
examination for newly joined person.
Periodic medical examination is conducted for all employees. The same is filed with the personnel
department. The employees are monitored for any open lesions and infectious disease (common
cold, nausea, fever etc.). Such employee is not allowed to perform the duties in the manufacturing
area unless he recovers from it and is certified by a Medical Practitioner in fitness.
All personnel working in the plant are required to maintain personal hygiene. All the persons
working in the manufacturing area must wear the appropriate protective clothing.
No eatables or drinks are allowed to warehouse or in manufacturing area. Smoking & chewing of
tobacco is strictly prohibited inside the warehouse or in manufacturing area.
A well – defined gowning procedure describing the procedure for gowning and change frequency is
in place. Separate Change Rooms are provided for Workmen and Staff. A laundry facility is used
for cleaning of clothing used for gowning.
Swati Spentose Pvt. Ltd.
22. Emergency Plan
Electrical Backup: The company has one generator for Critical power supply (Capacity
500KVA).
Water Backup for process: Storage tanks for GIDC potable water having the capacity 72 M³
which is capable to provide uninterrupted water supply to water system for more than three
days.
Water Backup in case of fire: Under ground storage tank of 285 M³ capacity in case of any
emergency in the factory consist main and jockey pump to keep the line pressurized for any
time use.
Personnel protective equipment: like helmet, shoe, safety glasses are mandatory in the
manufacturing area.
Emergency Plan: Onsite emergency plan is available in case of any crisis.
24 Hrs. Care: The organization is equipped with the Close circuit cameras (CCV) for the
continuous monitoring. The security and administration department in the premises of
organization gate are accessed by camera system which is continuously monitored to track
any unexpected occurrences of fire, accident and movement of manpower etc.
Safety measures: All the security and the fire safety are taken into action to prevent any loss
of the property and documents in the critical areas like Quality Assurance, RM Warehouse
and Finished goods warehouse.
Swati Spentose Pvt. Ltd.
23. FIRE PROTECTION AND SAFETY MEASURES
• We have adequate fire extinguishers (CO2 & DCP),
• Fire hydrant systems have been installed with 50 HP jockey pump,
• We provide safety trainings time to time to our team
• Fire fighting system is designed as per TAC norms
• We always keep hydrant line pressurized with Auto operation
system
• Adequate water reservoir is provided at list we can do firefighting
for 3 Hrs. until fire tender reached.
• We followed safety work permit system
Swati Spentose Pvt. Ltd.
I wish to extend a warm welcome on behalf of Swati Spentose, hers is a simple presentation about our facility and the policies, hope you will like it.
This is the front view of the unit, you can see two buildings in the picture. The first building having three manufacturing blocks, of which, one is dedicated production block for PPS, second is multipurpose block to run the different products on campaign basis, and third is pilot cum process development block having flexibility to play major roll in technology transfer for big volume products as well as low volume high cost products. Quality Control, Quality Assurance and Administrative Block are situated on the second floor of the same building. The second building is for all the utilities.
The group was started in the year 1952 and well known as Euresian Chemicals & Equipment, in 1970, our late chairman Shri Narayan Jajodia arrived in Mumbai to focus on API business. In 1996, we have started manufacturing of API bulk drug.
The Plant is located at Vapi, GIDC, 180 kms from Mumbai, in the western part of India which is also known as the financial capital of India. Vapi is very well connected by Road and Rail. The total area involves of around 6000 Sq. Meters, out of which about 4852 Sq. Meter is built up area.
This is the layout of VAPI GIDC Industrial estate.
The Effluent Treatment Plant has the capacity to treat 60 KL waste water per day. The quality of the original effluent and the quality of the effluent after the treatment is tabulated in this slide.
This is the method for treatment of the effluent. Effluent Treatment is carried out by removal of oil and grease, Neutralization, mixing and clarification primary, secondary and tertiary, aeration which helps to decrease the COD of waste water. The inorganic waste is disposed to the secure landfill through agency. The organic waste is sent for incineration to GPCB authorized facility. The effluent is periodically tested as per local laws for total dissolved solids, suspended solids, chemical oxygen demand, Biochemical oxygen demand, Chlorides, Sulphate, Ammonical Nitrogen, oil, grease and pH.
Different type of hazardous waste and the tentative generated quantity is given in this slide with disposal procedure.
This is the schematic drawing of the ETP plant, we will see during the facility tour.
Here is the policy for environmental management.
Tentative cost for maintaining the environmental plan.
Here is the Environmental, Health and safety (EHS) policy of the company, according to the policy, we are committed to preventing pollution through efficient use of resources. Greenery is promoted around the plant to get better environment. The environmental management system is in place to improve the overall environmental performance.
There are sufficient number of qualified employees in all the departments and further appropriate training is being provided to everyone. The responsibilities of all personnel engaged in the manufacture of intermediates and APIs are specified in writing. Induction training is compulsory for all the new employee and Periodic medical examination is conducted for each and every member of the company.
All Employees are trained on the requirements of good personal hygiene at the time of their induction Program and QA and department heads on a routine basis to monitor the same.