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LEUCINE
Bringing Efficiency To Pharma Compliance
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CLEANING VALIDATION IN THE PHARMACEUTICAL INDUSTRY
CLEANING VALIDATION IN THE PHARMACEUTICAL INDUSTRY
Cleaning validation has been the most debated compliance topic of the year 2018. Cleaning validation is a critical aspect of GMP and…
Vivek Gera
Jul 4, 2019
TOP 5 TRENDS IN NON-COMPLIANCE IN PHARMACEUTICAL MANUFACTURING
TOP 5 TRENDS IN NON-COMPLIANCE IN PHARMACEUTICAL MANUFACTURING
Pharmaceutical companies operate in one of the most dynamic environments. Changes in regulations by leading bodies such as US Food and…
Vivek Gera
Jul 4, 2019
HOW TECHNOLOGY CAN HELP SOLVE TOP 3 FDA COMPLIANCE CHALLENGES
HOW TECHNOLOGY CAN HELP SOLVE TOP 3 FDA COMPLIANCE CHALLENGES
Non-compliance is the biggest threat to the growth story of the Indian Pharmaceutical Industry today. The number of warning letters issued…
Vivek Gera
Jul 4, 2019
A Brief History Of 21 CFR Part 11: Electronic Records And Electronic Signatures
A Brief History Of 21 CFR Part 11: Electronic Records And Electronic Signatures
If you are connected to the life sciences industry in one way or another, you have undoubtedly heard of the USFDA’s 21 CFR Part 11…
Vivek Gera
Jul 4, 2019
DIGITISING CLEANING PROCEDURES: A $50 BILLION OPPORTUNITY
DIGITISING CLEANING PROCEDURES: A $50 BILLION OPPORTUNITY
Pharma Companies have a great opportunity to recover lost productivity, as much as $50 Billion every year, with very little changes in the…
Vivek Gera
Jul 3, 2019
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