The document provides details about an in-plant training conducted by students at Sula Vineyards Pvt. Ltd. The key points covered include:
1. The objectives of the training were to expose students to real-world work, learn new industrial methods, and improve their skills.
2. An overview of Sula Vineyards' wine preparation process, quality control checks, packaging materials analysis, and wine canning line is presented.
3. The training concluded that the students gained work experience, learned teamwork, and improved their problem-solving abilities.
Cost efficient Quality Management in Microbreweries can be achieved with basic, inexpensive instruments and measurements.
Many microbrewers face challenges with lack of time, money, and technical/QA knowledge. Quality is important to meet customer needs and expectations. Basic but useful measurements include original gravity, pH, alcohol content, color, bitterness, microbiology, raw materials, packaging quality, and customer satisfaction.
Simple logs of raw materials, mashing, fermentation and samples can provide quality control. Basic instruments under €2000 like refractometers, saccharometers, pH meters and microscopes can measure key parameters. Taste testing is also a powerful diagnostic tool. With limited investment, microbrewers can manage quality and consistency.
Sulphuric acid solution……..1.25g H2SO4/100ml. Concentration must be checked by titration.
Sodium hydroxide solution………1.25g NaOH/100ml. Concentration must be checked by titration.
Caution: Dust mask and gloves must be worn while handling chemicals. Always add acid to water and not the reverse.
validation of solid presentation by ahsan khanDRx Ahsan Khan
This document discusses validation of solid dosage forms such as tablets and capsules. It covers the key aspects of validation including validation of raw materials, analytical methods, equipment, and manufacturing processes. The manufacturing process involves various unit operations for tablets such as mixing, granulation, drying, lubrication, compression, and coating. In-process and finished product testing are also important parts of validation. Validation ensures a reproducible product that meets specifications.
The document provides guidance on good practices for HEB packaging quality processes. It outlines several golden rules for video meetings. It then details recommendations for various stages of quality control for HEB packaging, from reception of materials to online checks, release checks, and shelf life of materials. Specific tests are recommended, such as leak tests, dye penetrant tests, and seal strength tests. Record keeping, material specifications, supplier audits, and WFP compliance testing are also discussed. The overall aim is to ensure proper packaging integrity in order to increase shelf life of HEBs to 18 months.
Uttara Knitting & Dyeing Ltd. is a knit composite dyeing industry located in Gazipur, Bangladesh. It has 14 dyeing machines from Japan with a total dyeing capacity of over 3,000 kg. The dyeing machines include high temperature jet dyeing machines and atmospheric dyeing machines. The company also has laboratory facilities for dye testing including a light box, balances, iron, sample dyeing machine, washing machine, and pH tester. However, the dyeing laboratory is not very developed.
This document discusses the key stages in processing and packaging sterile products, including:
1) Processing, cleaning equipment, sterilization, compounding products, filtration, filling, sealing, and packaging.
2) The main processing stages include cleaning equipment thoroughly, sterilizing using methods like autoclaving, carefully compounding products, filtering solutions, precisely filling containers, sealing containers to maintain sterility, and final packaging.
3) Filling equipment is designed to precisely fill liquids and solids while maintaining sterility, and may include gravity fillers, pressure pump fillers, and vacuum fillers. Containers are sealed using methods like melting glass for ampoules or inserting rubber stoppers for vials.
Complete Information and knowledge about the selection criteria for packaging material and different test used for them .
All this material data is , Collected for seminar in QA SEM 2 , in the Subject of Pharmaceutical Manufacturing Technology .
Which also explain the How Quality control for Filling an pharmaceutical equipment is done.
Gap Inc. is a leading global apparel retailer founded in 1969 in San Francisco. It operates brands like Gap, Banana Republic, Old Navy, and Athleta. The document outlines Gap Inc.'s quality assurance policies and procedures for vendors, including standards for defects, inspection methods for materials, production processes, and final products. Vendors must meet Gap's requirements for safety, measurements, visual quality, and packaging to ship orders.
Cost efficient Quality Management in Microbreweries can be achieved with basic, inexpensive instruments and measurements.
Many microbrewers face challenges with lack of time, money, and technical/QA knowledge. Quality is important to meet customer needs and expectations. Basic but useful measurements include original gravity, pH, alcohol content, color, bitterness, microbiology, raw materials, packaging quality, and customer satisfaction.
Simple logs of raw materials, mashing, fermentation and samples can provide quality control. Basic instruments under €2000 like refractometers, saccharometers, pH meters and microscopes can measure key parameters. Taste testing is also a powerful diagnostic tool. With limited investment, microbrewers can manage quality and consistency.
Sulphuric acid solution……..1.25g H2SO4/100ml. Concentration must be checked by titration.
Sodium hydroxide solution………1.25g NaOH/100ml. Concentration must be checked by titration.
Caution: Dust mask and gloves must be worn while handling chemicals. Always add acid to water and not the reverse.
validation of solid presentation by ahsan khanDRx Ahsan Khan
This document discusses validation of solid dosage forms such as tablets and capsules. It covers the key aspects of validation including validation of raw materials, analytical methods, equipment, and manufacturing processes. The manufacturing process involves various unit operations for tablets such as mixing, granulation, drying, lubrication, compression, and coating. In-process and finished product testing are also important parts of validation. Validation ensures a reproducible product that meets specifications.
The document provides guidance on good practices for HEB packaging quality processes. It outlines several golden rules for video meetings. It then details recommendations for various stages of quality control for HEB packaging, from reception of materials to online checks, release checks, and shelf life of materials. Specific tests are recommended, such as leak tests, dye penetrant tests, and seal strength tests. Record keeping, material specifications, supplier audits, and WFP compliance testing are also discussed. The overall aim is to ensure proper packaging integrity in order to increase shelf life of HEBs to 18 months.
Uttara Knitting & Dyeing Ltd. is a knit composite dyeing industry located in Gazipur, Bangladesh. It has 14 dyeing machines from Japan with a total dyeing capacity of over 3,000 kg. The dyeing machines include high temperature jet dyeing machines and atmospheric dyeing machines. The company also has laboratory facilities for dye testing including a light box, balances, iron, sample dyeing machine, washing machine, and pH tester. However, the dyeing laboratory is not very developed.
This document discusses the key stages in processing and packaging sterile products, including:
1) Processing, cleaning equipment, sterilization, compounding products, filtration, filling, sealing, and packaging.
2) The main processing stages include cleaning equipment thoroughly, sterilizing using methods like autoclaving, carefully compounding products, filtering solutions, precisely filling containers, sealing containers to maintain sterility, and final packaging.
3) Filling equipment is designed to precisely fill liquids and solids while maintaining sterility, and may include gravity fillers, pressure pump fillers, and vacuum fillers. Containers are sealed using methods like melting glass for ampoules or inserting rubber stoppers for vials.
Complete Information and knowledge about the selection criteria for packaging material and different test used for them .
All this material data is , Collected for seminar in QA SEM 2 , in the Subject of Pharmaceutical Manufacturing Technology .
Which also explain the How Quality control for Filling an pharmaceutical equipment is done.
Gap Inc. is a leading global apparel retailer founded in 1969 in San Francisco. It operates brands like Gap, Banana Republic, Old Navy, and Athleta. The document outlines Gap Inc.'s quality assurance policies and procedures for vendors, including standards for defects, inspection methods for materials, production processes, and final products. Vendors must meet Gap's requirements for safety, measurements, visual quality, and packaging to ship orders.
PROCESS VALIDATION- AMPOULES, VIALS, ORAL PREPARATIONSalmanLatif14
This document discusses process validation for various pharmaceutical dosage forms and operations. It begins by defining process validation and its importance. It then provides details on validating different steps for products like ampoules, ointments, and liquid orals. These include validating washing, filling, sealing, sterilization, inspection, packaging, sampling, testing, and monitoring critical process parameters. The document also discusses validation protocols, reports, and references. The overall purpose is to establish documented evidence that specific processes will consistently produce pharmaceutical products meeting quality standards.
SMALL VOLUME PARENTRALS , MANUFACTURING AND QUALITY CONTROLDivya Thakur
This document discusses the formulation, manufacturing, and quality control of small volume parenterals (SVPs). It defines SVPs as injections packaged in containers of 100ml or less. The key points are:
SVPs can be single dose ampoules, multiple dose vials, or prefilled syringes. Their formulations typically include an aqueous, water-miscible, or non-aqueous vehicle along with buffers, preservatives, antioxidants, and tonicity adjusters. Manufacturing involves preparation, sterilization, filling, and sealing in clean rooms with proper air filtration and personnel flow. Quality control tests include particulate matter, leakage, clarity, sterility, pyrogen and endotoxin tests.
Varun Beverages Pvt. Ltd. is a franchisee of PepsiCo beverages in Nepal. It has a manufacturing plant in Kathmandu with 500 employees. The plant produces carbonated drinks like Pepsi, 7Up, and Mountain Dew as well as non-carbonated drinks like Tropicana and Mirinda. The internship summary describes the company's production processes including syrup preparation, blowing, filling, and packaging lines. It also discusses the plant's utilities like water treatment, power generation, air compression, and quality control procedures. The intern makes recommendations to improve production tracking, health and safety, and maintenance management.
Ammonia Plant Technology
Pre-Commissioning Best Practices
GBHE-APT-0102
PICKLING & PASSIVATION
CONTENTS
1 PURPOSE OF THE WORK
2 CHEMICAL CONCEPT
3 TECHNICAL CONCEPT
4 WASTES & SAFETY CONCEPT
5 TARGET RESULTS
6 THE GENERAL CLEANING SEQUENCE MANAGEMENT
6.6.1 Pre-cleaning or “Physical Cleaning
6.6.2 Pre-rinsing
6.6.3 Chemical Cleaning
6.6.4 Critical Factors in Cleaning Success
6.6.5 Rinsing
6.6.6 Inspection and Re-Cleaning, if Necessary
7 Systems to be treated by Pickling/Passivation
This document discusses cleaning and hygiene in the brewery, specifically focusing on Clean-In-Place (CIP) systems. It begins by acknowledging sources for some of its material and noting that content is based on the author's current opinion. The document then outlines its contents which include sections on the importance of hygiene, global brewing standards, definitions and types of CIP, cleaning verification tests, CIP plant design, and cleaning regime optimization.
The document discusses in-process quality control (IPQC) during pharmaceutical packaging operations. It describes various IPQC tests that should be performed at the start of each packaging batch, including protruding product sensor tests, pin hole detector tests, and leak tests. It also discusses barcode sensor tests that should be done every half hour to check cartons and leaflets. The key goal of IPQC is to provide early warnings for any quality issues during packaging and help ensure the packaged drugs maintain standards of identity, strength, quality and purity until consumption.
This document discusses in-process quality control. It defines quality and describes the in-process quality control process which includes understanding production parameters, creating control plans, monitoring parameters, reporting results, identifying defects, providing feedback, and correcting issues. It describes different types of in-process inspections and factors affecting inspections. The "4M's" of inspection - machine, method, material, and man - are also discussed as well as final inspections, sampling plans, quality control in distribution, acceptance quality limits, common defect types, and the importance of quality control.
This document outlines a Hazard Analysis and Critical Control Point (HACCP) plan for chocolate production. It identifies the key processing steps in chocolate making and potential physical, chemical, and biological hazards at each step. Critical control points are established to monitor for hazards, along with critical limits, monitoring procedures, corrective actions, and documentation requirements. The goal is to implement food safety controls to maximize product safety throughout the chocolate making process.
This document summarizes innovations at Grifols, a leading plasma fractionation company. It discusses Grifols' divisions and recent acquisitions. It then focuses on innovations across the plasma fractionation process, including automated plasma collection and bottle opening, large-scale pooling and fractionation using horizontal vessels, highly automated separation using centrifuges, modular skid-based purification, and a continuous sterile filling line. The innovations aim to improve efficiency, yields, quality and safety across the fractionation process.
Garments production process & quality assuranceKhalid Mehmood
The document describes the quality assurance process in garment production. It involves inspecting fabrics and accessories at various stages of production. This includes fabric inspection, testing of materials, and checking at key points like cutting, stitching, washing, finishing, and packing. The quality assurance team aims to ensure the right product is delivered on time while meeting customer requirements and standards through continuous monitoring and improvement.
The document provides details about setting up a packaged drinking water plant called Puro Water Plant. It discusses the three phases of setting up the plant over 12 months, including site engineering, infrastructure acquisition, and construction. It also outlines the plant's purification process, key management positions, marketing plan, target markets, promotional strategies, pricing strategy, and financial appraisal with projected costs and profits. The overall goal is to establish a trusted brand of packaged drinking water in Jammu, India.
This document provides an overview of the manufacturing process and export procedures for glass refills produced by Firozabad Glass Shell Industries. It begins with an executive summary and table of contents. It then discusses the company profile, history, manufacturing process involving 11 steps, quality procedures, environmental practices, and awards received. The document also outlines the key documents involved in export like the bill of lading and commercial invoice. It provides a high-level view of the glass refill production and export workflow of the company.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have strict quality control systems in place and certifications like ISO 9001, cGMP, and BRC. PET Power uses an injection stretch blow moulding process to produce bottles and jars in a cleanroom facility, and can provide gamma irradiation for sterilization. They offer various bottle and jar styles, sizes, and colors for pharmaceutical and medical applications.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow moulding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various laboratory services to support product development and regulatory requirements for their pharmaceutical customers.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow molding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various bottle styles, closures, and lab services to support customers' packaging needs.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have strict quality control systems in place and certifications like ISO 9001, cGMP, and BRC. PET Power uses an injection stretch blow moulding process to produce bottles and jars from PET resin in a cleanroom facility classified as ISO Class 7. Finished products undergo sterilization with gamma radiation to achieve a sterility assurance level of 10^-6.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow moulding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various laboratory services to support product development and regulatory requirements for their customers in the healthcare industry.
The document summarizes an internship project to improve operational efficiency at Hector Beverages Pvt Ltd. Data was collected on defects occurring after the filler station, primarily date coding issues. Analysis found date coding misalignment and missing codes were major defects, largely due to lack of synchronization between filling and coding speeds. Suggestions included fixing the sensor position and ensuring smooth filler flow to address misalignment, and sensor maintenance and manual checks to address missing codes.
Grifols is the third largest producer of plasma-derived medicines worldwide. They have developed novel technologies for plasma fractionation processes like pooling, fractionation, purification, and filling. Their innovations minimize clean room space and cold processing requirements while maximizing automation, closed processing, and natural lighting. Recent projects include expanding facilities in Clayton, North Carolina and Parets del Valles, Spain to incorporate these technologies and increase production capacity.
Heritage Conservation.Strategies and Options for Preserving India HeritageJIT KUMAR GUPTA
Presentation looks at the role , relevance and importance of built and natural heritage, issues faced by heritage in the Indian context and options which can be leveraged to preserve and conserve the heritage.It also lists the challenges faced by the heritage due to rapid urbanisation, land speculation and commercialisation in the urban areas. In addition, ppt lays down the roadmap for the preservation, conservation and making value addition to the available heritage by making it integral part of the planning , designing and management of the human settlements.
PROCESS VALIDATION- AMPOULES, VIALS, ORAL PREPARATIONSalmanLatif14
This document discusses process validation for various pharmaceutical dosage forms and operations. It begins by defining process validation and its importance. It then provides details on validating different steps for products like ampoules, ointments, and liquid orals. These include validating washing, filling, sealing, sterilization, inspection, packaging, sampling, testing, and monitoring critical process parameters. The document also discusses validation protocols, reports, and references. The overall purpose is to establish documented evidence that specific processes will consistently produce pharmaceutical products meeting quality standards.
SMALL VOLUME PARENTRALS , MANUFACTURING AND QUALITY CONTROLDivya Thakur
This document discusses the formulation, manufacturing, and quality control of small volume parenterals (SVPs). It defines SVPs as injections packaged in containers of 100ml or less. The key points are:
SVPs can be single dose ampoules, multiple dose vials, or prefilled syringes. Their formulations typically include an aqueous, water-miscible, or non-aqueous vehicle along with buffers, preservatives, antioxidants, and tonicity adjusters. Manufacturing involves preparation, sterilization, filling, and sealing in clean rooms with proper air filtration and personnel flow. Quality control tests include particulate matter, leakage, clarity, sterility, pyrogen and endotoxin tests.
Varun Beverages Pvt. Ltd. is a franchisee of PepsiCo beverages in Nepal. It has a manufacturing plant in Kathmandu with 500 employees. The plant produces carbonated drinks like Pepsi, 7Up, and Mountain Dew as well as non-carbonated drinks like Tropicana and Mirinda. The internship summary describes the company's production processes including syrup preparation, blowing, filling, and packaging lines. It also discusses the plant's utilities like water treatment, power generation, air compression, and quality control procedures. The intern makes recommendations to improve production tracking, health and safety, and maintenance management.
Ammonia Plant Technology
Pre-Commissioning Best Practices
GBHE-APT-0102
PICKLING & PASSIVATION
CONTENTS
1 PURPOSE OF THE WORK
2 CHEMICAL CONCEPT
3 TECHNICAL CONCEPT
4 WASTES & SAFETY CONCEPT
5 TARGET RESULTS
6 THE GENERAL CLEANING SEQUENCE MANAGEMENT
6.6.1 Pre-cleaning or “Physical Cleaning
6.6.2 Pre-rinsing
6.6.3 Chemical Cleaning
6.6.4 Critical Factors in Cleaning Success
6.6.5 Rinsing
6.6.6 Inspection and Re-Cleaning, if Necessary
7 Systems to be treated by Pickling/Passivation
This document discusses cleaning and hygiene in the brewery, specifically focusing on Clean-In-Place (CIP) systems. It begins by acknowledging sources for some of its material and noting that content is based on the author's current opinion. The document then outlines its contents which include sections on the importance of hygiene, global brewing standards, definitions and types of CIP, cleaning verification tests, CIP plant design, and cleaning regime optimization.
The document discusses in-process quality control (IPQC) during pharmaceutical packaging operations. It describes various IPQC tests that should be performed at the start of each packaging batch, including protruding product sensor tests, pin hole detector tests, and leak tests. It also discusses barcode sensor tests that should be done every half hour to check cartons and leaflets. The key goal of IPQC is to provide early warnings for any quality issues during packaging and help ensure the packaged drugs maintain standards of identity, strength, quality and purity until consumption.
This document discusses in-process quality control. It defines quality and describes the in-process quality control process which includes understanding production parameters, creating control plans, monitoring parameters, reporting results, identifying defects, providing feedback, and correcting issues. It describes different types of in-process inspections and factors affecting inspections. The "4M's" of inspection - machine, method, material, and man - are also discussed as well as final inspections, sampling plans, quality control in distribution, acceptance quality limits, common defect types, and the importance of quality control.
This document outlines a Hazard Analysis and Critical Control Point (HACCP) plan for chocolate production. It identifies the key processing steps in chocolate making and potential physical, chemical, and biological hazards at each step. Critical control points are established to monitor for hazards, along with critical limits, monitoring procedures, corrective actions, and documentation requirements. The goal is to implement food safety controls to maximize product safety throughout the chocolate making process.
This document summarizes innovations at Grifols, a leading plasma fractionation company. It discusses Grifols' divisions and recent acquisitions. It then focuses on innovations across the plasma fractionation process, including automated plasma collection and bottle opening, large-scale pooling and fractionation using horizontal vessels, highly automated separation using centrifuges, modular skid-based purification, and a continuous sterile filling line. The innovations aim to improve efficiency, yields, quality and safety across the fractionation process.
Garments production process & quality assuranceKhalid Mehmood
The document describes the quality assurance process in garment production. It involves inspecting fabrics and accessories at various stages of production. This includes fabric inspection, testing of materials, and checking at key points like cutting, stitching, washing, finishing, and packing. The quality assurance team aims to ensure the right product is delivered on time while meeting customer requirements and standards through continuous monitoring and improvement.
The document provides details about setting up a packaged drinking water plant called Puro Water Plant. It discusses the three phases of setting up the plant over 12 months, including site engineering, infrastructure acquisition, and construction. It also outlines the plant's purification process, key management positions, marketing plan, target markets, promotional strategies, pricing strategy, and financial appraisal with projected costs and profits. The overall goal is to establish a trusted brand of packaged drinking water in Jammu, India.
This document provides an overview of the manufacturing process and export procedures for glass refills produced by Firozabad Glass Shell Industries. It begins with an executive summary and table of contents. It then discusses the company profile, history, manufacturing process involving 11 steps, quality procedures, environmental practices, and awards received. The document also outlines the key documents involved in export like the bill of lading and commercial invoice. It provides a high-level view of the glass refill production and export workflow of the company.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have strict quality control systems in place and certifications like ISO 9001, cGMP, and BRC. PET Power uses an injection stretch blow moulding process to produce bottles and jars in a cleanroom facility, and can provide gamma irradiation for sterilization. They offer various bottle and jar styles, sizes, and colors for pharmaceutical and medical applications.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow moulding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various laboratory services to support product development and regulatory requirements for their pharmaceutical customers.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow molding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various bottle styles, closures, and lab services to support customers' packaging needs.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have strict quality control systems in place and certifications like ISO 9001, cGMP, and BRC. PET Power uses an injection stretch blow moulding process to produce bottles and jars from PET resin in a cleanroom facility classified as ISO Class 7. Finished products undergo sterilization with gamma radiation to achieve a sterility assurance level of 10^-6.
PET Power is a leading specialist in PET packaging that produces bottles and jars for the healthcare industry. They have a quality management system certified to ISO 9001 and cGMP standards. Products are produced using injection stretch blow moulding in a cleanroom classified as ISO Class 7. Finished products undergo quality control testing and can be gamma irradiated for sterilization. PET Power offers various laboratory services to support product development and regulatory requirements for their customers in the healthcare industry.
The document summarizes an internship project to improve operational efficiency at Hector Beverages Pvt Ltd. Data was collected on defects occurring after the filler station, primarily date coding issues. Analysis found date coding misalignment and missing codes were major defects, largely due to lack of synchronization between filling and coding speeds. Suggestions included fixing the sensor position and ensuring smooth filler flow to address misalignment, and sensor maintenance and manual checks to address missing codes.
Grifols is the third largest producer of plasma-derived medicines worldwide. They have developed novel technologies for plasma fractionation processes like pooling, fractionation, purification, and filling. Their innovations minimize clean room space and cold processing requirements while maximizing automation, closed processing, and natural lighting. Recent projects include expanding facilities in Clayton, North Carolina and Parets del Valles, Spain to incorporate these technologies and increase production capacity.
Heritage Conservation.Strategies and Options for Preserving India HeritageJIT KUMAR GUPTA
Presentation looks at the role , relevance and importance of built and natural heritage, issues faced by heritage in the Indian context and options which can be leveraged to preserve and conserve the heritage.It also lists the challenges faced by the heritage due to rapid urbanisation, land speculation and commercialisation in the urban areas. In addition, ppt lays down the roadmap for the preservation, conservation and making value addition to the available heritage by making it integral part of the planning , designing and management of the human settlements.
1. DADASAHEB MOKASHI COLLEGE OF FOOD
TECHNOLOGY, RAJMACHI
(Affiliated to Mahatma Phule Krishi Vidyapeeth, Rahuri)
Tal.- Karad, Dist.-Satara
Course No : FPO-487
STUDENT READY- INPLANT TRAINING
INDUSTRIAL PRESENTATION ON
SULA VINEYARDS PVT. LTD., JAULKE WANI
Presented by
GUNJAL NITIN DNYANESHVAR FTR-/2018
KUMBHAR YASH SUNIL FTR-39/2018
SHEJWAL SHUBHAM SHIVAJI FTR-63/2018
SHIROLE SANKET ANIL FTR-71/2018
Under the Guidance of : Mr. PATIL S.N. (Assistant Professor)
2. CONTENT
» Objectives
» About the company
» Wine Preparation
» Sanitation
» Line Check of Quality Control
» Packaging Material
» Wine in Can
» SAP
» Conclusion
2
3. 3
OBJECTIVES
» To expose students to a real-world working environment.
» To learn about new methods and industrial production.
» To prepare students for a professional career.
» To help students improve their technical, interpersonal and communication skills.
» To recruit new employees.
4. 4
HISTORY
• The name Sula derived from Rajeev Samant’s mother’s name “Sulabha.’’
• First winery set up in Nashik valley – 1998. Started with 5 acres.
• First harvest – 1999.
• First bottle of wine produced – 2000.
• Today 65% market share, sourcing from 3000 acres.
• In INDIA, sula introduced grape varieties namely sauvignon blanc, chenin
blanc for first time.
5. 5
THECOMPANY Company Sula Vineyards Pvt. Ltd.
Product Wine
Year of Establishment 1997
Registration no. 139352
Address Gate no. 90, Jaulake Wani,
Tal- Dindori, Dist- Nashik,
Maharashtra 422209
Telephone no. 2261280688
Email ID @sulalawines. com
Total Area 1800 Acres
Type of Ownership Public Company
Category of Processing Large Scale
Total Production/Day 300MT
6. 6
1. Human Resource and Administration
2. Marketing
3. Accounts and Finance
4. Store and Purchase
5. Viticulture
6. Winemaking
7. Quality Control
8. Project and Maintenance
9. Production
10. Effluent Treatment Plant
DEPARTMENTS
WINE PREPARATION
SANITITION
PACKAGING MATERIALS
PACKAGING MATERIALS
7. 7
WINEPREPARATIONPROCESS
Sanitized tank
Taking wine from
cellar
Addition of
nitrogen
Checking free
SO2
(Pre add)
Addition of KMS
Checking DO
(Pre)
Addition of CO2
Checking free
SO2
(Post add)
Checking DO
(Post)
Wine is ready for
bottling
For Still Wine:-
8. 8
For Sparkling Wine:-
Sanitized
pressurised tank
Taking wine from
cellar
Addition of
nitrogen
Checking free SO2
(Pre add)
Addition of KMS
&Citric acid
Checking free SO2
(Post add)
Giving pressure
using CO2
Checking pressure
Until get required
Rest the wine for
48hrs
Wine is ready for
bottling
9. 9
SANITATIONPROCEDURE
Hot water (85°C)
run from the tanks
Caustic soda run for
20 min (0.3%
caustic soda in 200
lit water (40°C)
After 20 min
removal of caustic
soda solution
Again run hot water
in the tanks
Adding citric acid
in tanks (0.3% citric
acid in 200 lit
water)
Running hot water
in tanks again
KMS solution
passed through
tanks (1% KMS in
200 lit water)
Running cold water
Detergents used for cleaning and
sanitation of tanks:
• Caustic soda
• Citric acid
• KMS
Fig: CIP flow chart
FOR TANKS:-
10. » Pre bottling Sanitation:-
• Running of hot water(above 80°C) for 30 min.
» Post bottling Sanitation:-
10
SANITATION PROCEDURE FOR LINES
Hot water (85°C)
run from the tanks
Caustic soda run for
20 min (0.3%
caustic soda in 200
lit water (40°C)
After 20 min
removal of caustic
soda solution
Again run hot water
in the tanks
Adding citric acid
in tanks (0.3% citric
acid in 200 lit
water)
Running hot water
in tanks again
KMS solution
passed through
tanks (1% KMS in
200 lit water)
Running cold water
12. » Examine Sanitation Procedure
» Checking SO2 Before bottling
» Filter Integrity
» Check DO & CO2
» Fill Log Sheets
» Line Audit
» FG Checklist
12
LINECHECKSOFQUALITYCONTROL
13. Linechecklist
» When the start-up line check the line audit before startup of line.
*In that first check the bottle feeding area.
* Then check the bottle wash area i.e nozzle check .
* After that check the bottle filling area and nozzle.
* Check the floor clean or not .
14. FinishGoodSheet
» After start of line fill the FG sheets i.e. Finish Good product check.
» OUTER BOX LABLE BOTTLE
1- State 1-Brand name & Vintage 1-Bottling Code
2-No. Of case 2-Batch no. 2- Screw cap seal & matter on cap
3- Brand name & Volume 3-MRP 3-Bottle condition
4- Batch no. 4- Alcohol 4-Hologram serial number
5- Address on Box 5-specific State 5- Fill height
6- Sula bop tape 6-Custmer care no. 6- Filled bottle inspection for FMC
7- Box condition 7- Label condition 7- Silica gel
8- No. Of staple 8- Remark
9- Bar code
10- Box printing quality
15. Torquecheck
» torque check – After the start up of line check the torque of first 5 bottle by torque machine. To avoid the
leakage of filled bottle & easily open to the customer .
Range of torque is depend on the type of bottle i.e. PET bottle and glass
also depends on size of bottle i.e. 180 ml 375 ml 750 ml .
Check the torque after every half hour and note down in the online
checklist sheet.
16. DPMO
» After start up of line check the DPMO every 2:00 hr.
» DPMO means Defect per million opportunities.
17. Dispatch
» Give the dispatch schedule from production office .
» Check the stock which is available in storage room In that check the box condition, bottle condition and check the lable
as per statutory file.
» After checking the product check vehicle condition and vehicle/driver documents .
» For the export dispatch check the product and vehicle condition as per checklist given by party.
20. » Packaging materials play an important role in quality control.
» Packaging Material used in Sula Vineyards.
1. Bottles.
2. Cartons.
3. Labels.
4. Screw Caps.
5. Tin-Can.
6. Corks.
7. Wire hoods.
20
PackagingMaterialAnalysis
21. » In Beverage Industry 750ml Bottle called as Quart, 375ml Bottles are called Pint and 180ml bottels are called as Nip.
» In Sula Vineyards following types of Bottles are Used.
1. BVS Bordeaux.
2. Burgundy.
3. Hock.
4. Champagne.
5. Dome Pet.
6. Round Pet.
21
Bottles:-
25. AnalysisOfBottle.
Checking all Following parameters as per given Specifications
1. Weight.
2. Height.
3. Neck OD With Threads.
4. Neck OD without Threads.
5. Neck ID.
6. Bore ID.
7. Tuck OD.
8. Below Tuck OD.
9. OD at 55mm.
10. OD at 59.5mm.
11. Body Diameter.
12. Torque.
13. Fill Height.
14. Brim Full Volume.
31. AnalysisofCarton:-
1. Weight.
2. Dimensions. (L×B×H)
3. GSM.
4. Number of Ply.
5. Number of flutes in 30cm.
6. Flute Height
7. Moisture.
8. Bursting Strength and Bursting Factor.
9. De-lamination.
10. Number of Staples.
11. Printing Matter.
12. Actual Fitment.
34. WINEINCAN
1. Feeding of empty can.
2. Rinsing of empty can.
3. Filling of wine.
4. Seaming of can.
5. coding .
6. Online weight check.
7. Box.
34
35. 1. Feeding of can
» In our winery feeding of can is done from manual method .
» Worker can depalletize the can and place it into conveyor .
» After that can travels from depalletized area to rinsing machine.
2. Rinsing of empty can :-
» After depalletization can come to rinsing .
» Rinsing is simply blow or flow water in empty can with pressure 0.75 bar’.
» If can is passed from rinser nozzle then blow air in can with the high pressure for removing all water drops from empty
can.
» After rinsing can goes to filling of wine .
35
36. Before filling precautions
» Before filling of wine it is must to check
DO(dissolve oxygen) & pressure of wine in buffer
tank .
» If wine is red then DO range between : 0.8-1.2
» If wine is white then Do ranges between : >0.8.
» pressure is same in between : 2.8-3.0.
36
Fillingofwine
After filling precaution
» Filling temperature of sparkling wine is :1-3
Celsius.
» After filling of wine DO also measure.
37. Seamingofcan
» Seaming is most important part of canning process.
» Seaming is judge by its seaming parameters like : overlap , wrinkle.
» Overlap is done in two operation
Seam analysis :-
First operation Second operation
37
38. Seamanalysiscalculation
» Seam analysis calculated by video camera method
» Video camera method –
Formula :-
• Actual overlap –
End hook +Body hook+(1.1*End thickness)- Seam length
• Overall seam analysis –
(cover hook + Body hook + 0.24)- seam height = greater than 0.75 then seaming is perfect.
38
39. Coding
» After seaming can passed below from coding machine head.
» coding is nothing but the printing of Batch no, Date of labeling &MRP etc.
» Date of Labeling mention in code format i.e
» 2 1 E 5 2
Year Date month
» 21E52 = 15th May 2022
coding machine
39
40. Onlineweightcheck
» Online check weighed is use for to check filled height or to detect present actual volume in can
» Basic calculation of weight check is :
» Empty can weight – 9.9gm
» seam weight –2.8gm
» Specific Density of Wine – 1
» Filled wine - 330ml
[ Empty can weight+ seam weight + Specific density of wine + Filled wine]
= If greater than or equal to 343.7 then machine pass bottle
Online weight check machine 40
41. SAP-
» SAP are having following modules
» Production –
» Quality –
» Sale –
» Purchasing –
» Dispatch –
1. production –
» Production are having specific movement type authorisation i.e.
1 .101
2. 102
3. Mb-51
4. COR1
5 . MB21
41
42. 42
CONCLUSION
» Gained knowledge and experience
» Learned team work and line handling responsibility
» Performed product analysis
» Working strength and time management
» Problem solving ability and basic SOP