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INTERVIEWS
Articles
Extractables and Leachables: Comprehensive Approaches to Controlling
17. December 2024
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Articles
Ethical Challenges and Solutions in Paediatric Drug Development
3. December 2024
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Articles
CMC Regulatory Compliance: Key Strategies, Guidelines, Role
26. November 2024
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Articles
The Role of CMC Statistics in Ensuring Pharmaceutical Product Quality and Compliance
30. September 2024
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Articles
Lipid-Based Formulations: Optimizing the Oral Delivery of Lipophilic Drugs
18. September 2024
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Articles
Mastering Risk Management in Medical Device Development: Key Strategies and Systems
10. September 2024
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Articles
Understanding and Controlling Bioburden: Definitions, Testing Procedures, and Best Practices
29. August 2024
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Articles
Good Clinical Practice in Pharma: Understanding GCP Compliance, Regulations, and Standards for Effective Clinical Trial
15. August 2024
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Articles
Process Validation in Pharmaceutical Industry
6. August 2024
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Articles
Extractables and Leachables Testing
25. July 2024
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Articles
What is the Difference between GLP and GMP
4. July 2024
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Interviews
Let’s Talk About Pharma | Inhalation Drug Products: Insights into Development, Challenges, and US & EU Regulatory Standards
18. April 2024
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Articles
What is CMC in Pharma?
3. April 2024
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Interviews
Let’s Talk About Pharma | CMO: Successful Outsourcing, KPIs & Supplier Relationship
13. February 2024
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Articles
Phases of Drug Development Process
23. November 2023
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Articles
Understanding GxP Regulations in Pharma
2. November 2023
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Articles
Strategic Decision-Making in Pharma: Training for Success
25. October 2023
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Interviews
Let’s Talk About Pharma | Real World Evidence: Why It’s Important & What’s The Future
24. September 2023
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Articles
What is Clinical Investigations and Evaluation
24. August 2023
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Articles
Latest Requirements for Aseptic Manufacturing of Pharmaceutical Products
20. July 2023
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