Validation Master Plan (VMP) In the Pharmaceutical Industry
Learn how to create a comprehensive Validation Master Plan (VMP) to ensure consistent product quality and regulatory compliance
Expiry Dates for Commercial and In-House Prepared Reagents In QC Labs
Discover the best practices for establishing and managing expiry dates for commercial and in-house prepared reagents in QC labs.
FDA Issues Warning Letter to LS Promotions Inc. for cGMP Violations
FDA issues warning to LS Promotions Inc. for significant cGMP violations. Learn about the key deficiencies, recommended CAPA plan, and steps for compliance.
Different Types of GMP Documentation Used In Pharma Industry
Explore the different types of GMP documentation in the pharmaceutical industry, essential for maintaining quality, compliance, and safety in manufacturing processes.