QC

Should acceptance criteria for residues be defined for dedicated equipment?

TELUGU GMP October 31, 2022

QC

Does ICH Q7 expect that the quality unit performs API release testing?

TELUGU GMP October 21, 2022

MEDICAL DEVICES

Who must register and submit medical device list to FDA?

TELUGU GMP October 17, 2022

USFDA

Some products, such as transdermal patches, are made using manufacturing processes with higher in-process material reject rates than for other products and processes. Is this okay?

TELUGU GMP October 10, 2022

USFDA

Can containers, closures, and packaging materials be sampled for receipt examination in the warehouse?

TELUGU GMP September 09, 2022

USFDA

Do CGMPs require a firm to retain equipment status identification labels with batch record or logs?

TELUGU GMP September 05, 2022

USFDA

FDA issued warning letters to 3 companies for selling unapproved new drugs

TELUGU GMP August 10, 2022

USFDA

Why does the FDA inspect and what does an FDA inspector do?

TELUGU GMP July 22, 2022

QC

If the FDA calls to inspect your facility tomorrow? in Telugu

TELUGU GMP July 09, 2022

GMP

EMA Good Pharmacovigilance Practices (GVP) Guidelines

TELUGU GMP July 09, 2022

QC

Quality Assurance Future Trends and Opportunities?

TELUGU GMP June 10, 2022

QC

What is staff training in Pharma and Life Sciences? in Telugu

TELUGU GMP May 19, 2022

QA

When should a supplier audit be conducted? in Telugu

TELUGU GMP May 13, 2022

QC

Reducing human errors in the manufacturing process in Telugu

TELUGU GMP May 09, 2022

QC

Making pharmaceutical manufacturing smart means? in Telugu

TELUGU GMP May 01, 2022