All Videos Channels
  1. Regulatory Affairs - Global Regulatory Harmonization for drugs & medical devices- IMDRF and ICMRA. Peivand Pirouzi, Ph.D.

    Regulatory Affairs - Global Regulatory Harmonization for drugs & medical devices- IMDRF and ICMRA. Peivand Pirouzi, Ph.D.

    36
  2. Regulatory Affairs - Health Canada CTA in CTD fromat - Completing the clinical trial attestation form. Peivand Pirouzi, Ph.D.

    Regulatory Affairs - Health Canada CTA in CTD fromat - Completing the clinical trial attestation form. Peivand Pirouzi, Ph.D.

    36
  3. Regulatory Affairs - Health Canada Form-0292-Medical Devices Establishment Licensing (MDEL) Application. P.Pirouzi, Ph.D.

    Regulatory Affairs - Health Canada Form-0292-Medical Devices Establishment Licensing (MDEL) Application. P.Pirouzi, Ph.D.

    12
  4. Healthcare Regulatory Affairs Outsourcing Market Business Scenario.

    Healthcare Regulatory Affairs Outsourcing Market Business Scenario.

    14
  5. Regulatory Affairs - Health Canada CTA in CTD format - Completing the clinical trial site information form. Peivand Pirouzi, Ph.D.

    Regulatory Affairs - Health Canada CTA in CTD format - Completing the clinical trial site information form. Peivand Pirouzi, Ph.D.

    33
  6. Regulatory Affairs - eCTD Submission Gateways for FDA and EMA, and ICH-M8 (Pharmaceutical Sciences and Health Care products). Peivand Pirouzi, Ph.D.

    Regulatory Affairs - eCTD Submission Gateways for FDA and EMA, and ICH-M8 (Pharmaceutical Sciences and Health Care products). Peivand Pirouzi, Ph.D.

    23
    1
  7. Regulatory Affairs - Completion of Health Canada form PSEAT for CTA application. Peivand Pirouzi, Ph.D.

    Regulatory Affairs - Completion of Health Canada form PSEAT for CTA application. Peivand Pirouzi, Ph.D.

    28
  9. Trump Accuses "Comrade Kamala" of "Regulatory Jihad"

    Trump Accuses "Comrade Kamala" of "Regulatory Jihad"

    2
    0
    18
  10. Regulatory Affairs Project Management: NDS in CTD Format for Health Canada by Peivand Pirouzi, Ph.D.

    Regulatory Affairs Project Management: NDS in CTD Format for Health Canada by Peivand Pirouzi, Ph.D.

    30
  11. Regulatory Affairs - EMA - Marketing Authorization Applications for Pharmaceutical Products in EU. Peivand Pirouzi, Ph.D.

    Regulatory Affairs - EMA - Marketing Authorization Applications for Pharmaceutical Products in EU. Peivand Pirouzi, Ph.D.

    33
  12. Regulatory Affairs - Health Canada Clinical Trial Application CTA in CTD format - Completing form 3011. P.Pirouzi, Ph.D.

    Regulatory Affairs - Health Canada Clinical Trial Application CTA in CTD format - Completing form 3011. P.Pirouzi, Ph.D.

    31
  13. Regulatory Affairs - FDA databases: Drugs@FDA and Clinical trials.gov - Live demonstrations - Peivand Pirouzi, Ph.D.

    Regulatory Affairs - FDA databases: Drugs@FDA and Clinical trials.gov - Live demonstrations - Peivand Pirouzi, Ph.D.

    23
  14. Senate Banking Housing and Urban Affairs Committee: Recent Bank Failures and the Federal Regulatory Response - March 28, 2023

    Senate Banking Housing and Urban Affairs Committee: Recent Bank Failures and the Federal Regulatory Response - March 28, 2023

    6
  15. HEARING: Economic Growth Energy Policy and Regulatory Affairs

    HEARING: Economic Growth Energy Policy and Regulatory Affairs

    2
  16. Regulatory Affairs - Clinical Trials Information System in Europe (EMA-Clinical Research). Peivand Pirouzi, Ph.D.

    Regulatory Affairs - Clinical Trials Information System in Europe (EMA-Clinical Research). Peivand Pirouzi, Ph.D.

    17
  17. Regulatory Affairs - Health Canada-Preparation of Meeting Application Packages for CTA,NDS,SNDS. Peivand Pirouzi, Ph.D.

    Regulatory Affairs - Health Canada-Preparation of Meeting Application Packages for CTA,NDS,SNDS. Peivand Pirouzi, Ph.D.

    34
  18. Regulatory Affairs and Quality Assurance - Pharmaceutical Inspections and Audits (Based on ICH-Q10). Peivand Pirouzi, Ph.D.

    Regulatory Affairs and Quality Assurance - Pharmaceutical Inspections and Audits (Based on ICH-Q10). Peivand Pirouzi, Ph.D.

    28
  19. The pharmaceutical industry spends 5 times more on lobbying and public affairs than the oil industry

    The pharmaceutical industry spends 5 times more on lobbying and public affairs than the oil industry

    18
  20. Drug regulatory affairs certification course demo class_Global Pharma Academy

    Drug regulatory affairs certification course demo class_Global Pharma Academy

    352
  22. Announcing’3 months online certification course in Drug regulatory affairs’ batch 7 #DRAcourse

    Announcing’3 months online certification course in Drug regulatory affairs’ batch 7 #DRAcourse

    363
  23. Join our 3 months online certification course in Drug Regulatory affairs batch 5

    Join our 3 months online certification course in Drug Regulatory affairs batch 5

    353
  24. Announcing ‘3 months certification course in drug regulatory affairs’ batch 8

    Announcing ‘3 months certification course in drug regulatory affairs’ batch 8

    352
  25. Announcing free demo class on ‘3 months online certification course in drug regulatory affairs’

    Announcing free demo class on ‘3 months online certification course in drug regulatory affairs’

    366