April 11, 2024
GMP Vs. cGMP: What Is The Difference?
Many who participate in the manufacturing of medical products may [...]
Author: Regina Fullin
April 4, 2024
What is CQV Validation? How To Ensure Quality & Compliance.
In industries like pharmaceuticals, biotechnology, and medical [...]
March 28, 2024
New Drug Development: What To Do Internally & What To Outsource
Technology startups in pharmaceutical production have numerous [...]
March 14, 2024
FDA Cosmetic Regulations: New Mandated Compliance Programs For Cosmetic Companies
In Mid-December 2023, the FDA published its final guidance under [...]
February 29, 2024
Why Should You Outsource Quality Audits?
Our Compliance Team review of the 2023 most frequently cited 483 [...]
February 22, 2024
Why Is Quality Management System Due Diligence Important?
Quality Management System (QMS) due diligence is crucial for [...]
February 15, 2024
FDA Proposes New Sterilization Requirements For Medical Devices
The industry is moving away from ethylene oxide (EtO) [...]
February 8, 2024
GxP Compliance: Guide To Create A Safe, Effective And Usable Plan
In the rapidly evolving landscape of industries such as [...]
February 1, 2024
AI In Medical Devices: How Does The FDA Regulate To Reduce Patient Risk?
AI (artificial intelligence) algorithms are now able to make [...]