1 Day Global GMP (Good Manufacturing Practices) Latest Updates Training Course: Incorporating Innovations from EMA, PIC/S, FDA, WHO, ANVISA, MHRA (ONLINE EVENT: July 8, 2026)

The main market opportunities include expanding pharmaceutical manufacturing that adheres to dynamic global GMP standards, conducting comprehensive training programs to ensure compliance, and ...
RAPS

FDA warns researchers and drugmakers for clinical study, GMP violations

The US Food and Drug Administration (FDA) has issued warning letters to two researchers for failing to meet good clinical practice (GCP) requirements and for not complying with their own trial ...
JD Supra

Won’t Get Fooled Again: FDA Tells a Drug Company Don't Rely on AI

Key Takeaways - The Food & Drug Administration issued a Warning Letter citing a drug company for inappropriate use of AI in ...
The National Law Review

GMP Certification Explained: What Manufacturers Need to Know in 2026

Resource clarifies NSF GMP, USP Verified, and FDA cGMP standards and how GMP certification drives trust, retailer approval, and Amazon compliance. IRVINE, CA, UNITED ...

Master Validation Plan for FDA and EU (Annex 15) cGMP Compliance Training Webinar (ONLINE EVENT & ON-DEMAND: June 2, 2026)

The life science industry faces opportunities in enhancing cGMP compliance by developing robust, risk-based Validation and Verification strategies. Training on creating effective Master Validation ...
The Herald-Times

2026 Guide to cGMP Compliance for Dietary Supplement and Cosmetic Manufacturers

Guide covers five core components of 21 CFR Part 111 quality systems, common FDA cGMP violations, and tips for unannounced inspections IRVINE, CA, UNITED STATES ...
Nasdaq

BIO-TECHNE ANNOUNCES SUBMISSION OF FDA DRUG MASTER FILE FOR EXCELLERATE GMP IPSC EXPANSION MEDIUM SUPPORTING STEM CELL THERAPY

MINNEAPOLIS, Dec. 20, 2023 /PRNewswire/ -- Bio-Techne Corporation (NASDAQ: TECH) today announced that it has filed a Drug Master File (DMF) with the U.S. Food and Drug Administration (FDA) for its ...