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Presentation on cross contamination
Clean In Place
EQUIPMENTS, Equipment may be defined as a physical entity which is used to carry out a general or sp...
Organization and personnel: 1. Personnel responsibilities Training, personal record. 2. Hygiene P...
Learn how aluminium liners safeguard sensitive products from moisture, oxygenc & UV exposure whi...
Rahul Dalvi M.pharmacy at Bharati vidyapeeth college of pharmacy, Kolhapur
This slide include detail information about Impurities,Sources of impurities and types of impurities...
intro, scope, merits, ich, who guidelines
Sources of Impurities in medicinal Compounds
Current Good Manufacturing Practices
What is Reactors? Reactors Type in Pharma Industries? Glass Lined Reactors GLR Making Process GLR V...
Detailed overview of Microbial Spoilage in Pharmaceutical Industry
sdsdsdsds
About the pharmacovilgilence
Types and Sources of impurities. Pharmaceutical Inorganic chemistry UNIT-I (Part-II) Impurities: Imp...
CGMP guidelines, CFR, CDER and CBER, PIC/S, Environment control in pharma industry, plant layout, ma...
Indian GMP Certification & WHO GMP Certification by Mr. Vishal Shelke https://youtube.com/visha...
brief history of GMP
This is the process that goes into making sure good quality medication is made.
good warehouse practice for the industry
Electric diaphragm pumps, also known as electric-operated double diaphragm pumps, are versatile devi...
Impurities in pharmaceutical substances
This presentation contain introduction to Good Distribution Practices Guideline. and Legal GDP requi...
