DarshanTalks Podcast

406 Avsnitt

1. No Clinical Trial Waste

   Publicerades: 2025-04-08
2. The Real Meaning of Audit-Readiness in Clinical Research

   Publicerades: 2025-04-06
3. Ordinary People Are Changing Medicine

   Publicerades: 2025-04-04
4. Investor Influence Can Trigger FCA Violations

   Publicerades: 2025-04-02
5. Sponsor to Organization vs. Direct Investigator Agreements: Pros & Cons

   Publicerades: 2025-03-31
6. Clinical Trial Site M&A: What Most Get Wrong

   Publicerades: 2025-03-29
7. Future-Proof Sites: SOS Insights Revealed

   Publicerades: 2025-03-27
8. Why Food M&A Deals Collapse—And How to Prevent It

   Publicerades: 2025-03-25
9. Non-Compliance Led to QOL Medical's $47M Settlement

   Publicerades: 2025-03-23
10. FDA Regulatory Submissions: Challenges, Trends, and Future Predictions

    Publicerades: 2025-03-21
11. How to do a VR promo check - Carly Schaecter gives us her advice

    Publicerades: 2025-03-19
12. Diversity Matters in Clinical Trials

    Publicerades: 2025-03-18
13. EMA’s LLM Guidelines Impact Life Sciences

    Publicerades: 2025-03-16
14. How to Network Like a Pro at Conferences

    Publicerades: 2025-03-12
15. Getting Ready for SOS 2025: FDA 483s, SOPs, and Site Survival

    Publicerades: 2025-03-10
16. Maximizing Site Value

    Publicerades: 2025-03-07
17. 5 Key Areas to Review in Clinical Trial Agreements

    Publicerades: 2025-03-05
18. Discussing Stem Cell Research Opportunities with a Research Site Owner

    Publicerades: 2025-03-03
19. Quality Management: A Must in Clinical Trial Contracts

    Publicerades: 2025-03-01
20. AI-Powered Chatbots in Pharma Sales and Education

    Publicerades: 2025-02-27