• All Discussions
•  Charles Thomas

  Medical Device Single Audit Program (MDSAP)

  sudharani sharma replied 1 year ago 2 Members · 2 Replies

  FDA
•  Charles Thomas

  What is the FDA drug approval process?

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  Some Facts About the Current Good Manufacturing Practices (CGMPs)

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  What do you mean by Hazard Analysis Critical Control Point (HACCP)?

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  What is an Investigational New Drug Application for FDA?

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  FDA Audit Program – What You Need To Know

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  FDA E6 (R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1)

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  Fair Packaging and Labeling Act (FPLA) – FDA 16 CFR Part 500

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  FDA Form 483 – Inspectional Observations and Citation

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  How the FDA Drugs Development & Approval Process Works

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  Current Good Manufacturing Practice (cGMP) and How to Use Them

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  The Ultimate Primer on FDA 21 CFR

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA
•  Charles Thomas

  Investigational Device Exemption (IDE) in Medical Devices

   Charles Thomas replied 1 year, 6 months ago 1 Member · 0 Replies

  FDA