2024 Cannabis Flower Ph.Eur Monograph: A Walkthrough
Explore the new 2024 Cannabis Flower Ph.Eur Monograph, setting new quality standards for medicinal cannabis from July 1, 2024.
Process Validation Lifecycle: Risk-Based Approach
Discover the essentials of Process Validation Lifecycle with a risk-based approach. Learn how to ensure product integrity from development to commercialization, meeting critical specifications.
Residual Solvents in GMP: Classes, Guidelines and Testing
Explore the classes and regulatory guidelines used in Residual Solvents testing in GMP.
Process Validation in GMP
Discover the essentials of Process Validation in GMP, ensuring pharmaceutical quality through scientific and regulatory practices.
Out of Specification Results: Dealing with OOS Investigations in Pharma
Learn about all the phases of addressing Out of Specification (OOS) results in the pharmaceutical industry
Cleaning Validation In the Pharmaceutical Industry
Explore the essentials of cleaning validation in the pharmaceutical industry, including all necessary steps, challenges, and regulatory standards.
5 Key Differences Between OOS, OOT and OOE Results
Look into the five key differences between OOS, OOT, and OOE results, the regulatory requirements and their importance in the GMP.
Quality Assurance vs. Quality Control in GMP: Key differences
Explore the critical differences between Quality Assurance and Quality Control in GMP and learn more about their role within the pharmaceutical industry.
User Requirement Specification: How to Create URS for Successful Equipment Procurement
Explore the essentials of User Requirement Specification (URS) for successful project execution. Learn to craft effective URS documents.