DarshanTalks Podcast

406 Episodo

1. No Clinical Trial Waste

   Publicado: 8/4/2025
2. The Real Meaning of Audit-Readiness in Clinical Research

   Publicado: 6/4/2025
3. Ordinary People Are Changing Medicine

   Publicado: 4/4/2025
4. Investor Influence Can Trigger FCA Violations

   Publicado: 2/4/2025
5. Sponsor to Organization vs. Direct Investigator Agreements: Pros & Cons

   Publicado: 31/3/2025
6. Clinical Trial Site M&A: What Most Get Wrong

   Publicado: 29/3/2025
7. Future-Proof Sites: SOS Insights Revealed

   Publicado: 27/3/2025
8. Why Food M&A Deals Collapse—And How to Prevent It

   Publicado: 25/3/2025
9. Non-Compliance Led to QOL Medical's $47M Settlement

   Publicado: 23/3/2025
10. FDA Regulatory Submissions: Challenges, Trends, and Future Predictions

    Publicado: 21/3/2025
11. How to do a VR promo check - Carly Schaecter gives us her advice

    Publicado: 19/3/2025
12. Diversity Matters in Clinical Trials

    Publicado: 18/3/2025
13. EMA’s LLM Guidelines Impact Life Sciences

    Publicado: 16/3/2025
14. How to Network Like a Pro at Conferences

    Publicado: 12/3/2025
15. Getting Ready for SOS 2025: FDA 483s, SOPs, and Site Survival

    Publicado: 10/3/2025
16. Maximizing Site Value

    Publicado: 7/3/2025
17. 5 Key Areas to Review in Clinical Trial Agreements

    Publicado: 5/3/2025
18. Discussing Stem Cell Research Opportunities with a Research Site Owner

    Publicado: 3/3/2025
19. Quality Management: A Must in Clinical Trial Contracts

    Publicado: 1/3/2025
20. AI-Powered Chatbots in Pharma Sales and Education

    Publicado: 27/2/2025