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The presentation is about documentation in the pharmaceutical industry. Many important topics are co...
THE DOWNSTREAM PROCESSING IN MICROBIAL FERMENTATION
Complaints: Complaints and evaluation of complaints, Handling of return good, recalling and waste di...
GLP
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cosmetic, regulatory provision, schedule M, condition of licence, schedule U, prohibition of certain...
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In the bustling locality of Kasba, Kolkata, Genesis Eduventure offers a standout option for those se...
drug master file and distribution record of drug in pharmaceutical industry and its types
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LACTOSE DEGRADATION
Bioavailability and bioequivalence testing
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The development of therapeutic biologics involves a streamlined approach for their formulation and d...
In Process Quality Control Tests For Capsules
good warehouse practice for the industry
This presentation focuses on defining processes , threads and different scheduling algorithms
USFDA process validation
good manufacturing practices for finished pharmaceuticals (21 CFR 211)
Regulatory requirements of BIOAVAILABLITY & BIOEQUIVALENCE STUDIES
This Slideshare Contain a Brief information about the How Auditing Of QA Department is considered a...
distillation methods .
sterility testing
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