Meredith Crabtree
Meredith Crabtree
Meredith Crabtree has over 25 years’ experience in regulated industries, ranging from Blood, Plasma, Tissue, Laboratory, Pharma, Medical devices, Cosmetics, Supplements, and Animal Health manufacturing and distribution. Meredith works as a Quality Consultant performing label reviews, 3rd party inspections, Consent Decree, and Recall support. She also performs regulatory assessments and Quality training. Meredith has a degree in Medical Technology and is currently obtaining a degree in Quality Systems.
Live Webinar
By: Meredith Crabtree
Nov. 21, 2024
SOPs - How to Write Them to Satisfy those Inspectors
Attending this training will help the participants understand the specific requirements and expectations of FDA inspectors, allowing them to develop SOPs that meet regulatory standards and demonst…
Industry: FDA Compliance Duration: 60 Minutes Time: 12:00 PM PDT | 03:00 PM EDT
By: Meredith Crabtree
Jan. 16, 2025
Developing and Implementing Quality Culture in the Organization and Why it’s Important
In today's regulatory landscape, a strong quality culture is essential for preventing compliance issues and ensuring consistent product quality. Regulatory bodies, including the FDA, increasingly…
Industry: Pharmaceutical Duration: 90 Minutes Time: 12:00 PM PDT | 03:00 PM EDT
By: Meredith Crabtree
Jan. 27, 2025
Performance of Root Cause Analysis, CAPA, and Effectiveness Checks
This comprehensive course offers essential knowledge and practical skills in root cause analysis, corrective and preventive actions (CAPA), and conducting effectiveness checks. Participants will l…
Industry: FDA Compliance Duration: 90 Minutes Time: 12:00 PM PDT | 03:00 PM EDT
Recorded Session
By: Meredith Crabtree
Recorded Session
FDA current recommendations related to timely initiation of and responses to recalls
We all shudder to say that dreadful “R” word. Recalls are costly and time-consuming to any organization, whether a manufacturer or distributor. Whether the facility is the …
Industry: FDA Compliance Duration: 75 Minutes
By: Meredith Crabtree
Recorded Session
Ensuring Safe and Effective Pharmaceutical Products: A Comprehensive Guide to ICH Q9 (R1) Quality Risk Management in the Pharmaceutical Industry
The purpose of ICH Q9 is to ensure a systematic and proactive approach to managing risks that may affect product quality, patient safety, and data integrity. It recognizes that risk management sho…
Industry: FDA Compliance Duration: 90 Minutes
By: Meredith Crabtree
Recorded Session
From Challenges to Compliance: Understanding Dietary Supplement Oversight by the FDA
The US FDA and Dietary Supplement Oversight" explores the crucial role of the U.S. Food and Drug Administration (FDA) in regulating the rapidly growing dietary supplement industry. This train…
Industry: FDA Compliance Duration: 90 Minutes