Tag: David Lim


Comparative Overview and Understanding of GCP, GLP and GMP

GCP/GLP/GMP: Comparative Overview and Understanding of FDA’s 3 Major Regulations Speaker: Dr. David Lim, Ph.D., RAC, ASQ-CQA Date: By invitation only Contact us to schedule a seminar at your convenience Time: At your convenience Where: Online Length: 90 minutes Learn How to Understand and Adequately Implement GLP, GCP, and cGMP Regulatory Requirements It is critical for the industry to accurately understand the requirements

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David Lim Proposal in 2008 to FDA and FDA's Release of the Report for Building an Effective NMDSS

United States Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) February 23, 2015 According to the FDA’s blog entitled “Moving Toward a National Medical Device Postmarket Surveillance System,”it clearly reveals a great improvement in the right direction toward a National Medical Device Postmarket Surveillance System. The FDA/CDRH also announces the report entitled “Strengthening Patient Care: Building an

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LIVE Seminar for FDA UDI Overview

FDA UDI Final Rule Last Updated: 2015-12-29