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Miss.Meredith Crabtree
Area Of Expertise : FDA Regulations as they pertain Pharma, Medical Device, Cosmetics, Biologics (Blood, Tissue, Plasma). Manufacturing and Distribution. Human products and Animal Health Products.
30 Years Of Experience
Training Industry : Life Sciences
Meredith Crabtree has over 25 years’ experience in regulated industries ranging from Pharma, Medical Device, Biologics, Laboratory testing, Cosmetics, and Supplements. She has worked in both manufacturing and distribution as well as Human Health and Animal Health. Meredith currently 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.
5 results Found
Live Webinar
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 emphasize the need for organizations to establish and maintain a ...
- Basic & Intermediate
- 90 Mins
- Feb 25, 2025
On-Demand Webinar
US FDA Formally Proposes Aligning Quality System Regulations with ISO 13485
The United States Food and Drug Administration (FDA) plays a crucial role in regulating medical devices to ensure their safety and effectiveness. In an effort to harmonize its regulatory framework with international standards, the FDA has proposed aligning its ...
- Basic & Advanced
- 90 Mins
Recorded Webinar
FDA - ICH Guideline Q9 R1 on Quality Risk Management
The training session aims to provide participants with an understanding of the International Council for Harmonization (ICH) Q9 guideline, with a focus on the revised version, ICH Q9(R1). Participants will learn about the principles, concepts, and application ...
- Basic & Advanced
- 90 Mins