This document contains questions from various units of the Industrial Pharmacy course. The units cover topics like preformulation studies, tablets, capsules, parenteral products, ophthalmic products, cosmetics, pharmaceutical aerosols, and packaging material science. The questions are short answer questions assessing key concepts from each unit, such as the definition of polymorphism, methods for tablet manufacturing, types of parenteral products and their formulation considerations, and factors influencing the selection of packaging materials. There are over 250 questions in total assessing knowledge across these important areas of industrial pharmacy.
This document provides information about an examination for B. Pharmacy I semester students at SNVPMV Library Faculty of Pharmacy.
The examination contains 3 parts: Part A contains 10 multiple choice questions worth 3 marks each, Part B contains 1 long answer question worth 14 marks, and Part C contains 5 long answer questions worth 8 marks each.
Part A covers topics like dosage forms, inhalations, posology calculations, eutectic mixtures, syrups vs elixirs, Stokes' law, therapeutic incompatibilities, advantages and disadvantages of suppositories, factors influencing dermal drug penetration, and the formula for simple ointment.
Part B covers definitions and preparation of suspensions, and factors affecting
This document contains 16 questions regarding various aspects of pharmaceutical dosage forms and tablet manufacturing processes. It asks about different types of tablets classified by route of administration and use, as well as the manufacturing process for uncoated tablets. It also inquires about terms related to tablet characterization and their effects on bioavailability. Further questions address topics like solubility, powder flowability, advantages of tablets over capsules, challenges of liquid dosage forms, powder characterization, granulation, factors for regulatory approval of dosage forms, uses of gelatin capsules, challenges of multiple solid forms, reasons for granulation and milling, how particle size and shape affect tablets, how bulk density affects tablets, measuring bulk density, granule manufacture methods, and the manufacture
This document contains information about pharmacy exams for Biopharmaceutics & Pharmacokinetics, Herbal Drug Technology, Medicinal Chemistry - III, Pharmaceutical Biotechnology, and Pharmacology-III.
It includes sample exam questions in multiple choice and short answer format covering topics like drug absorption, bioequivalence studies, herbal drug preparation, antibiotic classification, monoclonal antibodies, and pharmacokinetic parameters.
The document provides exam guidelines including answering all questions in part A, two questions in part B, and seven questions in part C for each subject. Various parts are allotted different mark values for a total exam marks of 75.
This document outlines the exam structure for the Pharmaceutical Microbiology subject for the B. Pharmacy III Semester (PCI) examination in May 2023. It is divided into three parts:
Part A contains 10 short answer questions worth 2 marks each. Part B contains 2 long answer questions worth 10 marks each. Part C contains 7 long answer questions worth 5 marks each. Students must answer all questions in Part A, any two questions in Part B, and any seven questions in Part C. The exam is worth a total of 75 marks and lasts 3 hours.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
This document provides information about an examination for B. Pharmacy I semester students at SNVPMV Library Faculty of Pharmacy.
The examination contains 3 parts: Part A contains 10 multiple choice questions worth 3 marks each, Part B contains 1 long answer question worth 14 marks, and Part C contains 5 long answer questions worth 8 marks each.
Part A covers topics like dosage forms, inhalations, posology calculations, eutectic mixtures, syrups vs elixirs, Stokes' law, therapeutic incompatibilities, advantages and disadvantages of suppositories, factors influencing dermal drug penetration, and the formula for simple ointment.
Part B covers definitions and preparation of suspensions, and factors affecting
This document contains 16 questions regarding various aspects of pharmaceutical dosage forms and tablet manufacturing processes. It asks about different types of tablets classified by route of administration and use, as well as the manufacturing process for uncoated tablets. It also inquires about terms related to tablet characterization and their effects on bioavailability. Further questions address topics like solubility, powder flowability, advantages of tablets over capsules, challenges of liquid dosage forms, powder characterization, granulation, factors for regulatory approval of dosage forms, uses of gelatin capsules, challenges of multiple solid forms, reasons for granulation and milling, how particle size and shape affect tablets, how bulk density affects tablets, measuring bulk density, granule manufacture methods, and the manufacture
This document contains information about pharmacy exams for Biopharmaceutics & Pharmacokinetics, Herbal Drug Technology, Medicinal Chemistry - III, Pharmaceutical Biotechnology, and Pharmacology-III.
It includes sample exam questions in multiple choice and short answer format covering topics like drug absorption, bioequivalence studies, herbal drug preparation, antibiotic classification, monoclonal antibodies, and pharmacokinetic parameters.
The document provides exam guidelines including answering all questions in part A, two questions in part B, and seven questions in part C for each subject. Various parts are allotted different mark values for a total exam marks of 75.
This document outlines the exam structure for the Pharmaceutical Microbiology subject for the B. Pharmacy III Semester (PCI) examination in May 2023. It is divided into three parts:
Part A contains 10 short answer questions worth 2 marks each. Part B contains 2 long answer questions worth 10 marks each. Part C contains 7 long answer questions worth 5 marks each. Students must answer all questions in Part A, any two questions in Part B, and any seven questions in Part C. The exam is worth a total of 75 marks and lasts 3 hours.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
This document provides an assignment for a research methodology course. It includes 6 questions assessing key concepts in research methods. Question 1 distinguishes between management decision and research problems and asks for examples. Question 2 classifies research designs and their distinguishing features with examples. Question 3 discusses the four levels of measurement and permissible statistical techniques for each. Question 4 explains data processing steps like editing, coding, classifying and tabulating through an example. Question 5 distinguishes between various research concepts in bullet points. Question 6 defines chi-square test of goodness of fit, precautions for its use and provides an example problem to solve.
This document outlines the structure and questions for a pharmaceutical product development exam, including:
- Section A contains 1 compulsory question asking for explanatory definitions of 10 pharmaceutical terms.
- Section B contains 3 questions worth 10 marks each, related to quality control sampling, pharmaceutical optimization techniques, and new drug delivery systems.
- Section C contains 7 questions worth 5 marks each, related topics include excipients for aerosol formulations, regulatory requirements for liquid products, solvents and solubilization, designing heat-sensitive injection formulations, adjusting pH of liquids, increasing stability of hydrolytically unstable parenterals, pharmaceutical applications of binders, and differentiating quality control and quality assurance. The final question discusses direct compression of
Indian standard specification laid down for sampling and testing of skin car...Dhwani Khandhar
This document outlines Indian Standard specifications for sampling and testing of skin care products, including face packs and skin powders. It describes the different types of face packs and their key characteristics. Requirements are provided for ingredients, description, testing, packaging and marking. Test methods are included in annexes for determining parameters like pH, stability, residue on evaporation, loss on drying, ash content and microbial purity. Requirements for skin powders include classification into body and face powders, with limits for solubility, ingredients and other quality parameters. Additional requirements are given for products seeking the ECO Mark for environment friendliness.
In this webinar, you will learn:
- The key issues in continuous manufacturing concerning excipients
- How those issues can be addressed
Detailed description:
Continuous manufacturing is a major trend in solid dose formulation. It shows economic and quality benefits, however, hurdles and challenges need to be tackled before getting there. This webinar will address these hurdles and challenges as they relate to excipients.
We will present how continuous manufacturing lines are set up and the benefits users have experienced from them. Feeding of especially small components of formulation combined with bad flow is a major challenge, as well as having a high number of components leading to many feeders. Our answer to these challenges are threefold: betting on multifunctional excipients, and on premixes, either as finished products or as customized projects.
Continuous Manufacturing - Issues and AnswersMilliporeSigma
The document discusses continuous manufacturing in the pharmaceutical industry. It begins with an overview of continuous manufacturing and examples of companies that have adopted the technology. It then discusses some of the challenges that excipients may face with continuous manufacturing, such as quality constraints and ensuring content uniformity and flow. The document proposes some solutions for these challenges, including using mannitol as a multifunctional excipient and developing binary premixes and customized premixes of excipients ready for continuous manufacturing processes. It argues that mannitol and particle engineered grades like Parteck® M are well-suited as enabling excipients for continuous manufacturing due to their properties like compressibility, disintegration, and low hygroscopicity
1
Name: Chem 9, Section:
Lab Partner: Experiment Date:
Synthetic Polymers and Plastics
Part A: Physical Characteristics
Find or choose one type of each of the following plastic polymers, and report the following
characteristics:
Plastic
number
Short Name
(HDPE,
LDPE, etc)
Clear
(yes or no)
Opaque
(yes or no)
Flexibility
(can be
bent?)
Durability
(hard or
soft)
Breakability
(can be
cracked?)
Recyclable
(yes or no)
1
2
3
4
5
6
7
Part B: Density Tests
Report for plastic samples in each liquid: sinks rapidly, sinks slowly, floats on top, floats below surface
Plastic
number
1:1 ethanol/water
density = 0.94 g/cm
3
Water
density = 1.0 g/cm
3
10% NaCl solution
density = 1.08 g/cm
3
1
2
3
4
5
6
Relative Plastic Densities:
Less than 0.94 g/cm
3
Less than 1.0 g/cm
3
Less than 1.08 g/cm
3
More than 1.08 g/cm
3
Ranking of densities:
(lowest) _______ _______ _______ _______ _______ _______ (highest)
2
Part C: Polymer Bouncy Balls
Polymer Ball composition Approximate height bounced Physical characteristics
Ball #1:
Ball #2
Ball #3
Questions
1. Which of the Big Six plastics was the most flexible?
2. Which of the Big Six plastics would be the best material for each of the following examples?
Use short names to identify each plastic (e.g. HDPE).
a replacement for a glass window ?
a take-out container for food?
a flexible, expandable bag for carrying items?
a lightweight bottle cap?
3. An unknown plastic floats in a 10% NaCl solution but sinks in water. What is the range of
possible density values this plastic may have? Suggest the composition of this plastic.
3
4. Why is it important to dislodge any adhering bubbles in the density tests?
5. PET plastic (number 1) is the most valuable waste plastic at the present time. Suggest a way
to separate it commercially from other waste plastics.
6. Sometimes plastic containers are made from two polymers and not just one. What would
happen to the water density test if HDPE and PVC were mixed?
7. Why are plastic recyclers very concerned about identifying the different polymers and not
mixing them together?
8. The figure below depicts polymerization of polystyrene (PS). Circle the original monomers
and determine how many monomers are present.
4
9. Polyvinylchloride (PVC) is composed of the vinyl chloride monomer. The monomer
structure and general reaction are shown at right.
Draw a polyvinyl chloride polymer composed of five
monomers arrange ...
This document provides personal and professional details of Dr. Sandeep Rai in 3 pages. It includes his contact information, educational qualifications, professional experience spanning over 25 years working with various companies in research and development roles, technical skills, publications, and other achievements. He has extensive experience in product development and application research of synthetic rubbers and lattices. Currently he works as Senior General Manager of R&D at Gujarat Reclaim and Polymers Limited.
This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the body’s response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
How to Make a Field Mandatory in Odoo 17Celine George
In Odoo, making a field required can be done through both Python code and XML views. When you set the required attribute to True in Python code, it makes the field required across all views where it's used. Conversely, when you set the required attribute in XML views, it makes the field required only in the context of that particular view.
ISO/IEC 27001, ISO/IEC 42001, and GDPR: Best Practices for Implementation and...PECB
Denis is a dynamic and results-driven Chief Information Officer (CIO) with a distinguished career spanning information systems analysis and technical project management. With a proven track record of spearheading the design and delivery of cutting-edge Information Management solutions, he has consistently elevated business operations, streamlined reporting functions, and maximized process efficiency.
Certified as an ISO/IEC 27001: Information Security Management Systems (ISMS) Lead Implementer, Data Protection Officer, and Cyber Risks Analyst, Denis brings a heightened focus on data security, privacy, and cyber resilience to every endeavor.
His expertise extends across a diverse spectrum of reporting, database, and web development applications, underpinned by an exceptional grasp of data storage and virtualization technologies. His proficiency in application testing, database administration, and data cleansing ensures seamless execution of complex projects.
What sets Denis apart is his comprehensive understanding of Business and Systems Analysis technologies, honed through involvement in all phases of the Software Development Lifecycle (SDLC). From meticulous requirements gathering to precise analysis, innovative design, rigorous development, thorough testing, and successful implementation, he has consistently delivered exceptional results.
Throughout his career, he has taken on multifaceted roles, from leading technical project management teams to owning solutions that drive operational excellence. His conscientious and proactive approach is unwavering, whether he is working independently or collaboratively within a team. His ability to connect with colleagues on a personal level underscores his commitment to fostering a harmonious and productive workplace environment.
Date: May 29, 2024
Tags: Information Security, ISO/IEC 27001, ISO/IEC 42001, Artificial Intelligence, GDPR
-------------------------------------------------------------------------------
Find out more about ISO training and certification services
Training: ISO/IEC 27001 Information Security Management System - EN | PECB
ISO/IEC 42001 Artificial Intelligence Management System - EN | PECB
General Data Protection Regulation (GDPR) - Training Courses - EN | PECB
Webinars: https://pecb.com/webinars
Article: https://pecb.com/article
-------------------------------------------------------------------------------
For more information about PECB:
Website: https://pecb.com/
LinkedIn: https://www.linkedin.com/company/pecb/
Facebook: https://www.facebook.com/PECBInternational/
Slideshare: http://www.slideshare.net/PECBCERTIFICATION
Gender and Mental Health - Counselling and Family Therapy Applications and In...PsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
Drug Discoveries and Challenges for Polymeric Medical Packaging Devicessemualkaira
Background of this study is to analyze different kind of challenges
are facing during stability studies of the product. Significance of
this study is whether the primary Medical Packaging devices are
compatible with the product or not. Basic methodology is used
wide ranges of Analytical testing required to avoid market complaint and financial loss of the company. Major findings of the studies are to provide solutions for the respective problems in different options. Inshort this Article is going to impact hugely those
are working in R&D and production line as well.
This document provides an assignment for a research methodology course. It includes 6 questions assessing key concepts in research methods. Question 1 distinguishes between management decision and research problems and asks for examples. Question 2 classifies research designs and their distinguishing features with examples. Question 3 discusses the four levels of measurement and permissible statistical techniques for each. Question 4 explains data processing steps like editing, coding, classifying and tabulating through an example. Question 5 distinguishes between various research concepts in bullet points. Question 6 defines chi-square test of goodness of fit, precautions for its use and provides an example problem to solve.
This document outlines the structure and questions for a pharmaceutical product development exam, including:
- Section A contains 1 compulsory question asking for explanatory definitions of 10 pharmaceutical terms.
- Section B contains 3 questions worth 10 marks each, related to quality control sampling, pharmaceutical optimization techniques, and new drug delivery systems.
- Section C contains 7 questions worth 5 marks each, related topics include excipients for aerosol formulations, regulatory requirements for liquid products, solvents and solubilization, designing heat-sensitive injection formulations, adjusting pH of liquids, increasing stability of hydrolytically unstable parenterals, pharmaceutical applications of binders, and differentiating quality control and quality assurance. The final question discusses direct compression of
Indian standard specification laid down for sampling and testing of skin car...Dhwani Khandhar
This document outlines Indian Standard specifications for sampling and testing of skin care products, including face packs and skin powders. It describes the different types of face packs and their key characteristics. Requirements are provided for ingredients, description, testing, packaging and marking. Test methods are included in annexes for determining parameters like pH, stability, residue on evaporation, loss on drying, ash content and microbial purity. Requirements for skin powders include classification into body and face powders, with limits for solubility, ingredients and other quality parameters. Additional requirements are given for products seeking the ECO Mark for environment friendliness.
In this webinar, you will learn:
- The key issues in continuous manufacturing concerning excipients
- How those issues can be addressed
Detailed description:
Continuous manufacturing is a major trend in solid dose formulation. It shows economic and quality benefits, however, hurdles and challenges need to be tackled before getting there. This webinar will address these hurdles and challenges as they relate to excipients.
We will present how continuous manufacturing lines are set up and the benefits users have experienced from them. Feeding of especially small components of formulation combined with bad flow is a major challenge, as well as having a high number of components leading to many feeders. Our answer to these challenges are threefold: betting on multifunctional excipients, and on premixes, either as finished products or as customized projects.
Continuous Manufacturing - Issues and AnswersMilliporeSigma
The document discusses continuous manufacturing in the pharmaceutical industry. It begins with an overview of continuous manufacturing and examples of companies that have adopted the technology. It then discusses some of the challenges that excipients may face with continuous manufacturing, such as quality constraints and ensuring content uniformity and flow. The document proposes some solutions for these challenges, including using mannitol as a multifunctional excipient and developing binary premixes and customized premixes of excipients ready for continuous manufacturing processes. It argues that mannitol and particle engineered grades like Parteck® M are well-suited as enabling excipients for continuous manufacturing due to their properties like compressibility, disintegration, and low hygroscopicity
1
Name: Chem 9, Section:
Lab Partner: Experiment Date:
Synthetic Polymers and Plastics
Part A: Physical Characteristics
Find or choose one type of each of the following plastic polymers, and report the following
characteristics:
Plastic
number
Short Name
(HDPE,
LDPE, etc)
Clear
(yes or no)
Opaque
(yes or no)
Flexibility
(can be
bent?)
Durability
(hard or
soft)
Breakability
(can be
cracked?)
Recyclable
(yes or no)
1
2
3
4
5
6
7
Part B: Density Tests
Report for plastic samples in each liquid: sinks rapidly, sinks slowly, floats on top, floats below surface
Plastic
number
1:1 ethanol/water
density = 0.94 g/cm
3
Water
density = 1.0 g/cm
3
10% NaCl solution
density = 1.08 g/cm
3
1
2
3
4
5
6
Relative Plastic Densities:
Less than 0.94 g/cm
3
Less than 1.0 g/cm
3
Less than 1.08 g/cm
3
More than 1.08 g/cm
3
Ranking of densities:
(lowest) _______ _______ _______ _______ _______ _______ (highest)
2
Part C: Polymer Bouncy Balls
Polymer Ball composition Approximate height bounced Physical characteristics
Ball #1:
Ball #2
Ball #3
Questions
1. Which of the Big Six plastics was the most flexible?
2. Which of the Big Six plastics would be the best material for each of the following examples?
Use short names to identify each plastic (e.g. HDPE).
a replacement for a glass window ?
a take-out container for food?
a flexible, expandable bag for carrying items?
a lightweight bottle cap?
3. An unknown plastic floats in a 10% NaCl solution but sinks in water. What is the range of
possible density values this plastic may have? Suggest the composition of this plastic.
3
4. Why is it important to dislodge any adhering bubbles in the density tests?
5. PET plastic (number 1) is the most valuable waste plastic at the present time. Suggest a way
to separate it commercially from other waste plastics.
6. Sometimes plastic containers are made from two polymers and not just one. What would
happen to the water density test if HDPE and PVC were mixed?
7. Why are plastic recyclers very concerned about identifying the different polymers and not
mixing them together?
8. The figure below depicts polymerization of polystyrene (PS). Circle the original monomers
and determine how many monomers are present.
4
9. Polyvinylchloride (PVC) is composed of the vinyl chloride monomer. The monomer
structure and general reaction are shown at right.
Draw a polyvinyl chloride polymer composed of five
monomers arrange ...
This document provides personal and professional details of Dr. Sandeep Rai in 3 pages. It includes his contact information, educational qualifications, professional experience spanning over 25 years working with various companies in research and development roles, technical skills, publications, and other achievements. He has extensive experience in product development and application research of synthetic rubbers and lattices. Currently he works as Senior General Manager of R&D at Gujarat Reclaim and Polymers Limited.
Similar to Industrial Pharmacy – I Questions.pptx (9)
This document provides an overview of wound healing, its functions, stages, mechanisms, factors affecting it, and complications.
A wound is a break in the integrity of the skin or tissues, which may be associated with disruption of the structure and function.
Healing is the body’s response to injury in an attempt to restore normal structure and functions.
Healing can occur in two ways: Regeneration and Repair
There are 4 phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. This document also describes the mechanism of wound healing. Factors that affect healing include infection, uncontrolled diabetes, poor nutrition, age, anemia, the presence of foreign bodies, etc.
Complications of wound healing like infection, hyperpigmentation of scar, contractures, and keloid formation.
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
How to Make a Field Mandatory in Odoo 17Celine George
In Odoo, making a field required can be done through both Python code and XML views. When you set the required attribute to True in Python code, it makes the field required across all views where it's used. Conversely, when you set the required attribute in XML views, it makes the field required only in the context of that particular view.
ISO/IEC 27001, ISO/IEC 42001, and GDPR: Best Practices for Implementation and...PECB
Denis is a dynamic and results-driven Chief Information Officer (CIO) with a distinguished career spanning information systems analysis and technical project management. With a proven track record of spearheading the design and delivery of cutting-edge Information Management solutions, he has consistently elevated business operations, streamlined reporting functions, and maximized process efficiency.
Certified as an ISO/IEC 27001: Information Security Management Systems (ISMS) Lead Implementer, Data Protection Officer, and Cyber Risks Analyst, Denis brings a heightened focus on data security, privacy, and cyber resilience to every endeavor.
His expertise extends across a diverse spectrum of reporting, database, and web development applications, underpinned by an exceptional grasp of data storage and virtualization technologies. His proficiency in application testing, database administration, and data cleansing ensures seamless execution of complex projects.
What sets Denis apart is his comprehensive understanding of Business and Systems Analysis technologies, honed through involvement in all phases of the Software Development Lifecycle (SDLC). From meticulous requirements gathering to precise analysis, innovative design, rigorous development, thorough testing, and successful implementation, he has consistently delivered exceptional results.
Throughout his career, he has taken on multifaceted roles, from leading technical project management teams to owning solutions that drive operational excellence. His conscientious and proactive approach is unwavering, whether he is working independently or collaboratively within a team. His ability to connect with colleagues on a personal level underscores his commitment to fostering a harmonious and productive workplace environment.
Date: May 29, 2024
Tags: Information Security, ISO/IEC 27001, ISO/IEC 42001, Artificial Intelligence, GDPR
-------------------------------------------------------------------------------
Find out more about ISO training and certification services
Training: ISO/IEC 27001 Information Security Management System - EN | PECB
ISO/IEC 42001 Artificial Intelligence Management System - EN | PECB
General Data Protection Regulation (GDPR) - Training Courses - EN | PECB
Webinars: https://pecb.com/webinars
Article: https://pecb.com/article
-------------------------------------------------------------------------------
For more information about PECB:
Website: https://pecb.com/
LinkedIn: https://www.linkedin.com/company/pecb/
Facebook: https://www.facebook.com/PECBInternational/
Slideshare: http://www.slideshare.net/PECBCERTIFICATION
Gender and Mental Health - Counselling and Family Therapy Applications and In...PsychoTech Services
A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
Chapter wise All Notes of First year Basic Civil Engineering.pptxDenish Jangid
Chapter wise All Notes of First year Basic Civil Engineering
Syllabus
Chapter-1
Introduction to objective, scope and outcome the subject
Chapter 2
Introduction: Scope and Specialization of Civil Engineering, Role of civil Engineer in Society, Impact of infrastructural development on economy of country.
Chapter 3
Surveying: Object Principles & Types of Surveying; Site Plans, Plans & Maps; Scales & Unit of different Measurements.
Linear Measurements: Instruments used. Linear Measurement by Tape, Ranging out Survey Lines and overcoming Obstructions; Measurements on sloping ground; Tape corrections, conventional symbols. Angular Measurements: Instruments used; Introduction to Compass Surveying, Bearings and Longitude & Latitude of a Line, Introduction to total station.
Levelling: Instrument used Object of levelling, Methods of levelling in brief, and Contour maps.
Chapter 4
Buildings: Selection of site for Buildings, Layout of Building Plan, Types of buildings, Plinth area, carpet area, floor space index, Introduction to building byelaws, concept of sun light & ventilation. Components of Buildings & their functions, Basic concept of R.C.C., Introduction to types of foundation
Chapter 5
Transportation: Introduction to Transportation Engineering; Traffic and Road Safety: Types and Characteristics of Various Modes of Transportation; Various Road Traffic Signs, Causes of Accidents and Road Safety Measures.
Chapter 6
Environmental Engineering: Environmental Pollution, Environmental Acts and Regulations, Functional Concepts of Ecology, Basics of Species, Biodiversity, Ecosystem, Hydrological Cycle; Chemical Cycles: Carbon, Nitrogen & Phosphorus; Energy Flow in Ecosystems.
Water Pollution: Water Quality standards, Introduction to Treatment & Disposal of Waste Water. Reuse and Saving of Water, Rain Water Harvesting. Solid Waste Management: Classification of Solid Waste, Collection, Transportation and Disposal of Solid. Recycling of Solid Waste: Energy Recovery, Sanitary Landfill, On-Site Sanitation. Air & Noise Pollution: Primary and Secondary air pollutants, Harmful effects of Air Pollution, Control of Air Pollution. . Noise Pollution Harmful Effects of noise pollution, control of noise pollution, Global warming & Climate Change, Ozone depletion, Greenhouse effect
Text Books:
1. Palancharmy, Basic Civil Engineering, McGraw Hill publishers.
2. Satheesh Gopi, Basic Civil Engineering, Pearson Publishers.
3. Ketki Rangwala Dalal, Essentials of Civil Engineering, Charotar Publishing House.
4. BCP, Surveying volume 1
Philippine Edukasyong Pantahanan at Pangkabuhayan (EPP) CurriculumMJDuyan
(𝐓𝐋𝐄 𝟏𝟎𝟎) (𝐋𝐞𝐬𝐬𝐨𝐧 𝟏)-𝐏𝐫𝐞𝐥𝐢𝐦𝐬
𝐃𝐢𝐬𝐜𝐮𝐬𝐬 𝐭𝐡𝐞 𝐄𝐏𝐏 𝐂𝐮𝐫𝐫𝐢𝐜𝐮𝐥𝐮𝐦 𝐢𝐧 𝐭𝐡𝐞 𝐏𝐡𝐢𝐥𝐢𝐩𝐩𝐢𝐧𝐞𝐬:
- Understand the goals and objectives of the Edukasyong Pantahanan at Pangkabuhayan (EPP) curriculum, recognizing its importance in fostering practical life skills and values among students. Students will also be able to identify the key components and subjects covered, such as agriculture, home economics, industrial arts, and information and communication technology.
𝐄𝐱𝐩𝐥𝐚𝐢𝐧 𝐭𝐡𝐞 𝐍𝐚𝐭𝐮𝐫𝐞 𝐚𝐧𝐝 𝐒𝐜𝐨𝐩𝐞 𝐨𝐟 𝐚𝐧 𝐄𝐧𝐭𝐫𝐞𝐩𝐫𝐞𝐧𝐞𝐮𝐫:
-Define entrepreneurship, distinguishing it from general business activities by emphasizing its focus on innovation, risk-taking, and value creation. Students will describe the characteristics and traits of successful entrepreneurs, including their roles and responsibilities, and discuss the broader economic and social impacts of entrepreneurial activities on both local and global scales.
Temple of Asclepius in Thrace. Excavation resultsKrassimira Luka
The temple and the sanctuary around were dedicated to Asklepios Zmidrenus. This name has been known since 1875 when an inscription dedicated to him was discovered in Rome. The inscription is dated in 227 AD and was left by soldiers originating from the city of Philippopolis (modern Plovdiv).
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1. Industrial Pharmacy – I
(BP502T)
Questioners
By Ankita Burande
Assistant Professor
Nagpur College of Pharmacy Nagpur
2. Unit1: Preformulation Studies
Questions : (10 x 2 = 20 Marks)
What is Racemization? Give example.
Write the methods to study of solid forms of a substance
What is the need of preformulation studies in pharmaceutical product
development?
Write the differences between crystalline and amorphous forms of solid.
Define preformulation studies.
Write the BCS classification of drugs.
What is preformulation study
Define bulk density and write its importance in Pharmacy
3. Unit1: Preformulation Studies
Questions : (2 x 10 = 20 Marks)
(a) Discuss about crystallinity of solid substances. (b) Describe the
chemical reactions involved in degradation of API
Explain the study of physical characteristics during preformulation
Questions : (7 x 5 = 35 Marks)
How flow properties of powders are measured?
Explain polymorphism.
Write a note on polymorphism and its applications.
What is BCS classification? Discuss its importance.
4. Unit 2: Tablets
Questions : (10 x 2 = 20 Marks)
Explain friability test for tablets.
Explain the importance of enteric coating of tablet.
Describe the granulation methods for tablet manufacturing.
Classify tablets and give ideal characteristics of tablets.
What are the unofficial tests for evaluation of tablets.
Define Enteric coating and give its advantages.
Define buccal and sublingual tablets.
Enlist various types of coating materials of tablets.
Why coating tablets are required
Classify tablets.
What is Orange peel effect in tablet coating
5. Unit 2: Tablets
Questions : (2 x 10 = 20 Marks)
a) Describe the compression cycle for tablet manufacturing. (b) Explain in
process quality control tests for tablet compression.
(a) Explain perforated coating pans. (b) Write a brief note on filing of
capsules.
Enlist the excipients used in tablet manufacture with examples. Write their
role and mechanism of action.
Explain quality control tests of tablets.
(a) Explain about disintegration and dissolution test for tablets. (b) Write in
detail about evaluation of containers
6. Unit 2: Tablets
Questions : (7 x 5 = 35 Marks)
Discuss the steps involved in sugar coating of tablets
Discuss the tablet additives with examples of each class.
Explain about hardness and friability testing of tablets.
Write a brief note on manufacturing defects in tablet coating.
Explain weight variation test and content uniformity test for capsules
Explain sugar coating of tablets.
Explain defects in tablet coating
7. Unit 2: Liquid Orals
Questions : (10 x 2 = 20 Marks)
What are the tests used for detecting type of emulsion
Give formulation of suspension
Define emulsion & suspension
Questions : (7 x 5 = 35 Marks)
Describe the evaluation of liquid orals as per pharmacopoeia
Write the differences between flocculated and deflocculated
suspensions.
Discuss the method for preparation of emulsion.
Explain formulation considerations of liquid dosage forms.
Write a brief note on filling and packaging of oral liquids.
8. Unit 3: Capsules
Questions : (10 x 2 = 20 Marks)
Write the differences between type A and type B gelatin
Outline the steps of manufacturing of hard gelatin capsule SHELL
Write a note on sizes of hard gelatin capsules
Mention different sealing methods for hard gelatin capsules
Define Base adsorption
Questions : (2 x 10 = 20 Marks)
Explain in detail about manufacturing of hard gelatin capsules and soft gelatin capsules.
(a) Explain perforated coating pans. (b) Write a brief note on filing of capsules.
Explain the formulation and quantity control tests for hard gelatin or soft gelatin
capsules
(a) Write in brief about the manufacture of Aerosols. (b) Explain about the defects in
capsules.
9. Unit 3: Capsules
Questions : (7 x 5 = 35 Marks)
Describe the manufacturing defects of hard gelatin capsules
Explain weight variation test and content uniformity test for capsules.
Explain method of preparation of hard gelatin capsule shell.
Describe the manufacturing of soft gelatin capsules.
10. Unit 3: Pellets
Questions : (10 x 2 = 20 Marks)
Write the advantages of pellets.
Enlist the pelletization techniques
What are pellets? Give advantages of pellets
Questions : (7 x 5 = 35 Marks)
Explain in detail about extrusion-spheronization technique
Enlist techniques of pelletization. Explain advantages of pallets over
conventional dosage forms.
Write a note on palletization process.
Write in detail about solution layering.
Explain powder and liquid layering methods for pelletization, with a note
on equipment used for the same.
11. Unit 4: Parenteral products
Questions : (10 x 2 = 20 Marks)
Explain the concept of aseptic processing
Plastic bottles are preferred over glass bottles for saline. Justify.
Write the type of glass with their uses for pharmaceutical products
What is isotonicity? Explain its importance for parenteral products.
Write the principle involved in LAL test for injectables
What are Tonicity modifiers
Write the significance of isotonicity in parenterals
What are the vehicles used in the preparation of parenterals?
Classify parenteral with suitable examples.
What are pyrogens?
What is aseptic area?
What are the vehicles used in the preparation of parenterals.
Classify parenteral with suitable example
12. Unit 4: Parenteral products
Questions : (2 x 10 = 20 Marks)
(a) Describe sterility test procedures as per official books. (b) Discuss formulation considerations for
ophthalmic products.
(a) Explain pyrogen test for parenterals. (b) Discuss about the formulation of pharmaceutical aerosols.
Write a note on production facilities required for parenteral preparations.
Give the layout for manufacture of parenteral formulations
Explain formulation and the production of parenterals.
Questions : (7 x 5 = 35 Marks)
Elaborate the parenteral additives with their examples.
What are pyrogens? Discuss the pyrogen test for injectables.
Elaborate water attack test USP and powder glass test USP for packaging glass.
Discuss quality control of parenteral products.
Write a note on LAL test & sterility test.
Explain the process of freeze drying.
Write a note on injectable suspensions
13. Unit 4: Ophthalmic Products
Questions : (10 x 2 = 20 Marks)
What are the special instructions to be printed on the eye drop container
according to drugs and cosmetics act.
Questions. (2 x 10 = 20 Marks)
(a) Describe sterility test procedures as per official books. (b) Discuss
formulation considerations for ophthalmic products.
Questions. (7 x 5 = 35 Marks)
Explain Draize eye test for opthalmics.
Explain sterility test for ophthalmic products.
Write a note on formulation & lebelling of eye drops
Explain quality control tests of eye ointment
ite a note on formulation & lebelling of eye drops
14. Unit 5: Cosmetics:
Questions. (10 x 2 = 20 Marks)
Define cosmetics and give classification of cosmetics with examples
List out various ingredients used in tooth paste.
List out various ingredients used in tooth paste
What is the difference between cold cream & Vanishing cream.
How sunscreen products help to protect skin against UV radiation?
Questions. (2 x 10 = 20 Marks)
a) Elucidate the manufacturing of lipstick. (b) What are the possible interactions
between content and packaging material.
Questions. (7 x 5 = 35 Marks)
Discuss the manufacturing, and uses of cold cream and vanishing cream
Describe ingredients for toothpaste manufacturing
Write the formulation of cold cream.
Write a note on formulation of hair dyes.
15. Unit 5: Pharmaceutical Aerosols:
Questions. (10 x 2 = 20 Marks)
Illustrate the components of aerosol system with the help of neat diagram.
Define Propellant.
What are different types of aerosols?
Questions. (2 x 10 = 20 Marks)
(a) Describe the components of aerosol system with the help of a neat diagram. (b)
Discuss the types of aerosol system.
a) Explain pyrogen test for parenterals. (b) Discuss about the formulation of
pharmaceutical aerosols.
(a) Write in brief about the manufacture of Aerosols. (b) Explain about the defects
in capsules.
Explain the formulation and evaluation of aerosols.
Questions. (7 x 5 = 35 Marks)
Write a brief note on propellants in Aerosols
16. Unit 5: Packaging Material Science
Questions. (10 x 2 = 20 Marks)
Write the type of glass with their uses for pharmaceutical products
What are the different materials used for packaging?
Questions. (2 x 10 = 20 Marks)
a) Elucidate the manufacturing of lipstick. (b) What are the possible interactions
between content and packaging material
Questions. (7 x 5 = 35 Marks)
Explain the criteria for selection of packaging materials.
Explain the factors affecting selection of pharmaceutical packaging materials.
Write a note on factors influencing choice of containers