DarshanTalks Podcast

406 Folgen

1. No Clinical Trial Waste

   Vom: 8.4.2025
2. The Real Meaning of Audit-Readiness in Clinical Research

   Vom: 6.4.2025
3. Ordinary People Are Changing Medicine

   Vom: 4.4.2025
4. Investor Influence Can Trigger FCA Violations

   Vom: 2.4.2025
5. Sponsor to Organization vs. Direct Investigator Agreements: Pros & Cons

   Vom: 31.3.2025
6. Clinical Trial Site M&A: What Most Get Wrong

   Vom: 29.3.2025
7. Future-Proof Sites: SOS Insights Revealed

   Vom: 27.3.2025
8. Why Food M&A Deals Collapse—And How to Prevent It

   Vom: 25.3.2025
9. Non-Compliance Led to QOL Medical's $47M Settlement

   Vom: 23.3.2025
10. FDA Regulatory Submissions: Challenges, Trends, and Future Predictions

    Vom: 21.3.2025
11. How to do a VR promo check - Carly Schaecter gives us her advice

    Vom: 19.3.2025
12. Diversity Matters in Clinical Trials

    Vom: 18.3.2025
13. EMA’s LLM Guidelines Impact Life Sciences

    Vom: 16.3.2025
14. How to Network Like a Pro at Conferences

    Vom: 12.3.2025
15. Getting Ready for SOS 2025: FDA 483s, SOPs, and Site Survival

    Vom: 10.3.2025
16. Maximizing Site Value

    Vom: 7.3.2025
17. 5 Key Areas to Review in Clinical Trial Agreements

    Vom: 5.3.2025
18. Discussing Stem Cell Research Opportunities with a Research Site Owner

    Vom: 3.3.2025
19. Quality Management: A Must in Clinical Trial Contracts

    Vom: 1.3.2025
20. AI-Powered Chatbots in Pharma Sales and Education

    Vom: 27.2.2025