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
Pharmaceutical companies operate in one of the most dynamic environments.
Make your GMP processes compliant & efficient by design using data-driven strategies & insights.