Pharmaceuticals & Biologics

What is GMP Environmental Monitoring Management and How it Helps the Pharmaceutical Industry?

What is GMP Environmental Monitoring Management and How it Helps the Pharmaceutical Industry? By :Dr. Dhriti Tupe, GxP Expert ® In…

10 months ago

How to Improve Your Ability to Read Nutrition Research?

Improving your ability to read nutrition research can enhance your understanding of food science and help you make more informed…

10 months ago

Drug-Device Combination Products: Methodologies for User Interface Evaluation

Drug-Device Combination Products: Methodologies for User Interface Evaluation The development of drug-device combination products (DDCPs) has become a pivotal aspect…

10 months ago

Quality Control vs Quality Assurance vs Total Quality Management: Understanding Their Role and Importance in the Pharmaceutical Industry

Quality Control vs Quality Assurance vs Total Quality Management: Understanding Their Role and Importance in the Pharmaceutical Industry By :Dr.…

10 months ago

In Vitro Release Test (IVRT) for In Situ Gel/Depot-Forming Drug Products

In Vitro Release Test (IVRT) for In Situ Gel/Depot-Forming Drug Products Introduction: In situ gel and depot-forming drug products have…

10 months ago

Detailed Explanation of Teriparatide Generic Approval Process

Detailed Explanation of Teriparatide Generic Approval Process Peptide Drug Characterization: An Essential Step The FDA's focus on peptide drug characterization…

10 months ago

ALCOA vs. ALCOA++: Understanding Data Integrity in the Pharmaceutical Industry

ALCOA vs. ALCOA++: Understanding Data Integrity in the Pharmaceutical Industry By :Dr. Dhriti Tupe, GxP Expert ® Data integrity is the…

10 months ago

Explore 5 lucrative intellectual property career paths for science graduates. Discover how to leverage your scientific expertise in patent law, technology transfer, and IP management.

Explore 5 lucrative intellectual property career paths for science graduates. Discover how to leverage your scientific expertise in patent law,…

10 months ago

Why Risk Assessment and Mitigation Controls Reporting is Mandatory for QA and How to Handle It

Why Risk Assessment and Mitigation Controls Reporting is Mandatory for QA and How to Handle It? By :Dr. Dhriti Tupe,…

10 months ago

Cluster Development Programme (CDP) & Data Governance: Why It’s Mandatory and How to Handle It in the Pharmaceutical Industry

Cluster Development Programme (CDP) & Data Governance: Why It's Mandatory and How to Handle It in the Pharmaceutical Industry By…

11 months ago