Effectively Reviewing GMP Documents: A 10-Step Guide
Good manufacturing practice (GMP) documents are the backbone of pharmaceutical quality systems. It serves as controlled records that ensure consistency, traceability, and compliance with regulatory standards. We have prepared a comprehensive guide on how to review GMP...
What are Good Documentation Practices (GDP)? Basics & Pro Tips
Good documentation practices (GDP) describe best practices for creating and maintaining documentation in both paper and electronic format. These practices are used in pharmaceutical industry, medical device industry, and laboratories. It is basically a set of good...
Schedule M Compliance: Mandatory for Pharma Companies
Mandatory Schedule M compliance is being enforced to establish India as a global pharmaceutical manufacturing hub. The Schedule M is aimed increasing the accountability of pharmaceutical manufacturers for the quality and efficacy of the pharmaceutical products. The...