ASQ Medical Device Auditor (CMDA) Exam | How to Prepare
Click Here---> https:\/\/bit.ly\/3OqYdTM <---Get complete detail on CMDA exam guide to crack Auditing. You can collect all information on CMDA tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Auditing and get ready to crack CMDA certification. Expl
8 views • 20 slides
Optimize Your Preparation for the ASQ Medical Device Auditor (CMDA) Exam
Click Here--- https:\/\/bit.ly\/3OqYdTM ---Get complete detail on CMDA exam guide to crack Medical Device Auditor. You can collect all information on CMDA tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Medical Device Auditor and get ready to crac
2 views • 18 slides
How to Study for ASQ Calibration Technician (CCT) Certification Exam
Click Here--- https:\/\/bit.ly\/3HFBYpa ---Get complete detail on ASQ exam guide to crack Calibration Technician. You can collect all information on ASQ tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Calibration Technician and get ready to crack
3 views • 13 slides
Pharmaceutical-Contract-Development-and-Manufacturing-Market
In addition, the growing demand for cell and gene therapies and personalized medicines and growth in the High-potency Active Pharmaceutical Ingredients (HPAPI) and Antibody-drug Conjugates (ADC) markets are expected to offer significant opportunities for the growth of the pharmaceutical contract dev
1 views • 4 slides
Change Control in Pharmaceutical Industry
Change control in the pharmaceutical industry is a critical process that ensures the management of alterations to maintain product quality and compliance with regulatory standards. It involves categorizing changes as minor, major, or critical, each requiring specific handling to minimize risks and u
2 views • 14 slides
Pharmaceutical Processing Equipment Market
Pharmaceutical processing includes a range of unit operations such as blending, milling, granulation, tablet pressing, coating, and filling, depending on the mode of delivery. With the growing adoption of continuous manufacturing and the rising number of novel therapies in clinical development, phar
1 views • 2 slides
Understanding Physiological Acid-Base Balance in Pharmaceutical Inorganic Chemistry
This lecture delves into the fundamental concepts of pharmaceutical inorganic chemistry, focusing on the mechanisms and uses of various pharmaceutical products that correct body disorders. Topics covered include acids and bases, intra and extracellular electrolytes, and the role of buffers in mainta
9 views • 14 slides
Understanding Pharmaceutical Calculations and Laboratory Apparatus
Pharmaceutical preparations must be effective, safe, and accurate in both quantitative and qualitative aspects. This includes ensuring the accurate amount and identity of ingredients. Laboratory apparatus such as mortar and pestle, wide mouth bottles, cylindrical and conical measure cylinders, and c
4 views • 20 slides
Understanding Pharmaceutical Calculations: Altering Product Strength and Solutions
Pharmaceutical calculations involve altering the strength of pharmaceutical preparations by adjusting the proportion of active ingredients, using stock solutions, and problem-solving techniques. This process includes dilution, fortification, and concentration changes to achieve desired product stren
7 views • 23 slides
CPGP Study Guide and How to Crack Exam on Pharmaceutical GMP Professional
Click Here--- \/\/bit.ly\/4bsglWA ---Get complete detail on CPGP exam guide to crack Pharmaceutical GMP Professional. You can collect all information on CPGP tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Pharmaceutical GMP Professional and get r
3 views • 35 slides
ASQ Pharmaceutical GMP Professional (CPGP) Exam | Boost Your Score
Click Here---> \/\/bit.ly\/4bsglWA <---Get complete detail on CPGP exam guide to crack Pharmaceutical GMP Professional. You can collect all information on CPGP tutorial, practice test, books, study material, exam questions, and syllabus. Firm your knowledge on Pharmaceutical GMP Professional and get
0 views • 20 slides
Pharmaceutical Manufacturing Company in India | Unimarck
Our focus is to provide reliable manufactured products that are well-certified by reputable organizations like WHO and GMP. To provide a diverse range of products like quality tablets, syrups, and capsules, our company is working hard to meet high standards in its manufacturing process.
1 views • 4 slides
Top PCD Pharma Franchise Company in India | WHO GMP Certified
Unibiotech Formulations is WHO GMP Certified Pharma Franchise Company in India. We offer Latest formulations in tablets, capsules, suspensions, syrup, etc. Get more info for franchise Services Contact us at 917814301804
2 views • 5 slides
Understanding GMP Audits in Construction: Navigating Client Expectations
This presentation at the National Association of Construction Auditors' virtual conference focuses on helping clients grasp the key objectives and processes of Guaranteed Maximum Price (GMP) audits. Dave Potak, a seasoned professional, will share insights on managing client expectations, best practi
0 views • 18 slides
Guidelines for Personnel Training and Hygiene in Pharmaceutical Manufacturing
Personnel responsibilities in a manufacturing unit include training, hygiene, and maintaining personal records. Guidelines as per Sch.M of D&C act 1945 outline the supervision, qualifications, and duties required for technical staff, QC lab, and QA personnel. Health, clothing, and sanitation protoco
2 views • 16 slides
Understanding Thermogravimetric Analysis (TGA) in Pharmaceutical Applications
Thermogravimetric Analysis (TGA) is a technique that measures weight changes in a material as it is heated or cooled. This analysis helps in understanding decomposition, stability, and purity of pharmaceutical compounds. TGA operates on the principle of monitoring mass changes with temperature, offe
0 views • 27 slides
Microbiological Quality Control in Pharmaceutical Environment
Microbiological products in pharmaceutical settings are influenced by the quality of materials and the environment. Good Manufacturing Practices (GMP) are essential to minimize contamination risks, with control points focused on the ecology of microorganisms. Sources of contamination include the atm
1 views • 128 slides
Top WHO-GMP-ISO Certified Monopoly Pharma Franchise Company
Top WHO-GMP-ISO Certified Monopoly Pharma Franchise Company in India. Contact Unibiotech Formulations At 917814301804, 919216901651
1 views • 5 slides
Inorganic Pharmaceutical Chemistry: Applications and Importance
Inorganic pharmaceutical chemistry explores the study of elements and compounds excluding carbon, with diverse applications in pharmacy. It encompasses the synthesis and use of inorganic compounds in drug development, catalysis, pigments, and agriculture. The field also delves into the medicinal val
1 views • 6 slides
ASEAN Guidelines on GMP for Traditional Medicines: Evaluation of Corrective Action and Preventive Action
The ASEAN Guidelines on GMP for Traditional Medicines discuss the importance of Corrective Action and Preventive Action (CAPA) for maintaining quality in health supplements. CAPA involves identifying nonconformities, implementing solutions, and preventing future occurrences through continuous improv
1 views • 47 slides
Understanding Differential Thermal Analysis (DTA) in Pharmaceutical Applications
Differential Thermal Analysis (DTA) is a technique used in pharmaceutical applications to monitor temperature differences between a sample and reference material. By analyzing temperature changes over time or against temperature, DTA helps in detecting phase transitions and reaction temperatures in
0 views • 22 slides
Managing Microbiological Quality in Pharmaceutical Environments
The quality of microbiological products is influenced by the pharmaceutical environment materials. Good Manufacturing Practices (GMP) play a crucial role in minimizing contamination risks. Various sources of contamination include the atmosphere, water, persons, raw materials, packaging, buildings, a
0 views • 128 slides
WHO-GMP, GLP, ISO Certified Pharma Manufacturing Company
Unimarck Pharma is WHO-GMP, GLP, ISO Certified Pharma Manufacturing Company Since 1984. Contact us today at 91-172-2244500.
1 views • 5 slides
Excessive Pricing in Pharmaceutical Markets: The Italian Experience
The presentation by Andrea Pezzoli explores the issue of excessive pricing in pharmaceutical markets, focusing on the Italian experience. It covers cases of infringement on excessive prices, such as the Aspen pharmaceutical group's fine for unfair pricing. The regulatory framework in Italy, includin
4 views • 22 slides
India's Significant Contributions to Global Healthcare Through Pharmaceutical Exports
India, a key player in the global pharmaceutical sector, significantly contributes to global health through its pharmaceutical exports. The country provides generic medicines to over 200 countries, with a notable presence in highly regulated markets. India's pharmaceutical exports showcase impressiv
7 views • 7 slides
Understanding Pharmaceutical Chemistry: A Comprehensive Overview
Pharmaceutical chemistry delves into the study of drugs, encompassing their development, discovery, synthesis, absorption, metabolism, and more. It involves the design and synthesis of biologically active molecules to create new pharmaceuticals or enhance existing drug structures. Chemistry plays a
0 views • 5 slides
ASEAN Guidelines on GMP for Traditional Medicines/Health Supplements - Preparation for Inspection
This content provides guidelines on preparing for a Good Manufacturing Practice (GMP) inspection for traditional medicines and health supplements in ASEAN countries. It covers activities such as planning inspections, forming inspection teams, reviewing documentation, preparing inspection plans, hold
0 views • 19 slides
ASEAN Guidelines on GMP for Traditional Medicines - Preparation of GMP Report
The ASEAN Guidelines on GMP for Traditional Medicines provide detailed instructions on preparing GMP reports, including post-inspection activities, deficiency classification, examples of deficiencies, and inspection report format. Deficiencies are categorized as Critical, Major, or Minor, with speci
0 views • 20 slides
ASEAN Guidelines on GMP for Traditional Medicines - Philosophy of Inspection
The ASEAN Guidelines on GMP for Traditional Medicines highlight the Philosophy of Inspection for ensuring quality and safety in traditional medicines and health supplements. The document covers legal terms, audit trail requirements, electronic signature control, and familiar auditor requirements. It
0 views • 88 slides
Enhancing Feed Safety Through GMP+ International Certification
Explore the world of GMP+ International certification for feed safety, providing value to former foodstuffs. Learn how food companies can ensure safe feed practices, with a focus on compliance, incident management, and traceability. Discover the chain approach in various industries, from cultivation
0 views • 12 slides
Understanding Pharmaceutical Suspensions: Types, Preparation, and Characteristics
Explore the world of pharmaceutical suspensions, including their types based on dosage form and particle size, advantages of using suspensions, features desired in pharmaceutical suspensions, and classification based on the nature of solids involved in the suspension. Learn about the preparation met
0 views • 12 slides
ASEAN Guidelines on GMP for Traditional Medicines/Health Supplements: Conducting GMP Inspection
The ASEAN Guidelines provide detailed procedures for conducting GMP inspections to ensure objectivity and appropriateness. The inspection processes include opening meetings, facility inspections, documentation review, inspector meetings, and exit meetings. During the opening meeting, the inspection
0 views • 30 slides
ASEAN Guidelines on GMP for Traditional Medicines - Classification of GMP Non-Conformance
Classification of GMP non-conformance is crucial for conducting inspections and preparing reports. It helps companies take necessary actions and affects the inspection rating. The guidelines outline critical, major, minor, and other deficiencies in traditional medicines and health supplements, empha
0 views • 26 slides
Quality Issues in Clinical Trial Materials: CMC Review by Dr. Dorota Matecka
Clinical trial materials undergo Chemistry, Manufacturing, and Controls (CMC) review to ensure pharmaceutical quality. This process includes assessing safety concerns, impurities, and specifications, along with other CMC considerations. Pharmaceutical quality encompasses the suitability, identity, s
0 views • 41 slides
Pharmaceutical Calculation and Compounding Course Overview
This course provides pharmacy students with a foundation in pharmaceutical calculations including concentration expressions, density, isotonicity, and more. The curriculum focuses on practical skills essential for pharmacy practice. Students will learn how to handle medicinal prescriptions and perfo
0 views • 46 slides
Practical Advances in Pharmaceutical Analysis Using Spectroscopy Techniques
This comprehensive guide covers various spectroscopy techniques, including UV-Vis and IR spectroscopy, as well as electrochemical analysis and flame photometry, for pharmaceutical analysis. It delves into the fundamentals of molecular spectroscopy, discussing electromagnetic radiation, quantum energ
0 views • 19 slides
RAC Exam I Test Questions
The RAC Exam I Test Questions cover various aspects of regulatory affairs and compliance in the pharmaceutical industry. The questions touch on topics such as GMP, FDA regulations, product approvals, and legal requirements. Test your knowledge with these 100 questions to enhance your understanding o
0 views • 101 slides
ASEAN Guidelines on GMP for Traditional Medicines - Preparation for Inspection
This content outlines the preparation activities for a Good Manufacturing Practice (GMP) inspection for Traditional Medicines/Health Supplements as specified by the ASEAN Guidelines. It covers the objectives, processes, inspection team formation, documentation review, and other key aspects involved
0 views • 19 slides
Understanding Buffers in Pharmaceutical Formulations
Buffers in pharmacy play a critical role in maintaining constant pH levels essential for drug stability and efficacy. They resist pH changes by neutralizing added acids or bases, ensuring proper drug delivery and patient comfort. Common buffer systems, such as acetic acid/sodium acetate and boric ac
4 views • 18 slides
Update on Pharmaceutical Manufacturing Plan for Africa by Dr. Djoudalbaye Benjamin
The update on pharmaceutical manufacturing plan for Africa discusses the TRIPS agreement, the inception of the Pharmaceutical Manufacturing Plan for Africa (PMPA), and the importance of promoting access to quality healthcare through local pharmaceutical manufacturing in Africa.
0 views • 25 slides