August 22, 2024
What Is Pharma Serialization?
Counterfeit medication is a worldwide problem. Many of us in the [...]
Author: CTI Chat
July 25, 2024
Why You Need A Quality System Manual
If you work in an industry that manufactures medicinal products, [...]
July 11, 2024
What Is CAPA? Ultimate Guide To FDA Corrective And Preventive Actions
In today’s highly regulated industries, maintaining product [...]
June 13, 2024
FDA Warning Letters: How To Respond
In the complex landscape of regulatory oversight in the United [...]
April 11, 2024
GMP Vs. cGMP: What Is The Difference?
Many who participate in the manufacturing of medical products may [...]
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 [...]