Vivek GerainleucineCLEANING VALIDATION IN THE PHARMACEUTICAL INDUSTRYCleaning validation has been the most debated compliance topic of the year 2018. Cleaning validation is a critical aspect of GMP and…Jul 4, 2019Jul 4, 2019
Vivek GerainleucineTOP 5 TRENDS IN NON-COMPLIANCE IN PHARMACEUTICAL MANUFACTURINGPharmaceutical companies operate in one of the most dynamic environments. Changes in regulations by leading bodies such as US Food and…Jul 4, 2019Jul 4, 2019
Vivek GerainleucineHOW TECHNOLOGY CAN HELP SOLVE TOP 3 FDA COMPLIANCE CHALLENGESNon-compliance is the biggest threat to the growth story of the Indian Pharmaceutical Industry today. The number of warning letters issued…Jul 4, 2019Jul 4, 2019
Vivek GerainleucineA Brief History Of 21 CFR Part 11: Electronic Records And Electronic SignaturesIf 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…Jul 4, 2019Jul 4, 2019
Vivek GerainleucineDIGITISING CLEANING PROCEDURES: A $50 BILLION OPPORTUNITYPharma Companies have a great opportunity to recover lost productivity, as much as $50 Billion every year, with very little changes in the…Jul 3, 2019Jul 3, 2019