Leucine Micro Articles

FDA has issued a Form 483 to the J&J Vaccine manufacturing site of Emergent. Here are the key takeaways.

Currently, there are two approaches to evaluate Cleaning Agents toxicology. Lets evaluate both in this blog.

All major regulators have revised the Cleaning Validation Guidelines in the last 2 years. Here is a complete list.

Pharma Companies have a great opportunity to recover lost productivity, as much as $50 Billion every year

FDA gave electronic signatures legal equivalence with traditional “wet ink” signatures on paper in 1997.

Non-compliance is the biggest threat to the growth story of the Indian Pharmaceutical Industry today