Common Pitfalls in CSV Documentation and How to Avoid Them
CSV documentation is essential for compliance and data integrity in regulated industries. This blog explores common pitfalls such as incomplete records, lack of standardization, and poor version control, providing practical tips to help organizations maintain accuracy and avoid costly compliance errors.
5 Essential Components of GMP for Every Pharma Professional
Good Manufacturing Practices (GMP) form the foundation of quality assurance in the pharmaceutical industry. This article covers the five essential components of GMP that every pharma professional must understand to maintain compliance, ensure product safety, and consistently meet regulatory standards.
