Unimarck Pharma India's Best Pharma Products Manufacturers in Chandigarh. We are WHO-GMP, GLP, and ISO certified. 40 years of experience in this industry.

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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

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Unibiotech Formulations offer different types of Pharma products all over India for PCD Pharma Franchise. Unibiotech is WHO-GMP certified Pharma Franchise company. Call us Today @ 917814301804, 919216901651.\n\n\n

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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

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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.

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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

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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

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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

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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

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Top WHO-GMP-ISO Certified Monopoly Pharma Franchise Company in India. Contact Unibiotech Formulations At 917814301804, 919216901651

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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

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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

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Unimarck Pharma is WHO-GMP, GLP, ISO Certified Pharma Manufacturing Company Since 1984. Contact us today at 91-172-2244500.

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Good Laboratory Practices (GLP) is a quality system ensuring non-clinical health and environmental safety studies are conducted accurately and reliably. GLP promotes the validity of test data for determining safety of chemicals, pharmaceuticals, food, and cosmetics. This article explores the definit

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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

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This detailed study explores the extraction of glycomacropeptide (GMP) and securing casein curd from skim milk. It covers the composition of milk, the classification of milk proteins, the role of rennet in curd formation, and the history and preparation of rennet. Additionally, it delves into the us

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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

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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

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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

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Boiling Target Study conducted at Kent State University focused on analyzing the impact of beam current on target density fluctuations, termed as Boiling. The study involved applying various cuts, calculating live time, and extracting charge yield data to determine the presence of target boiling. Su

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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

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Pharma Franchise Company For Start Your Pharma Business. Unibiotech Formulations, a WHO-GMP certified PCD Pharma company in India. Call 7814301804, 9216901651 For Full Details.

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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

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In a dairy plant, maintaining good manufacturing practices (GMP) is crucial for ensuring quality and safety of products. This includes emphasizing personnel hygiene, cleanliness, and preventing contamination. Employees must adhere to strict personal hygiene practices, such as proper grooming and wea

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This content outlines the interim waiver process and scheduling procedures for local office client audits during the Corona outbreak. It includes steps for completing waiver applications, conducting remote audits, and handling certification extensions. The document also provides guidelines for remot

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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

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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

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