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An Interactive Workshop on Design Control for Medical Devices Including In Vitro Diagnostic Devices Subject: At this workshop, Dr. David Lim will walk you through to get familiar with...
Posted 6/27/2012 11:13:17 AM
GMP Training Documentation: If It Isn't Documented, It Didn't Happen Subject: The FDA has made it clear that, for drugs and devices, GMP training must be...
Posted 3/21/2011 10:01:49 AM
Critical Lessons in Risk Management: The Rising Impact of REMS Subject: Although risk management processes, particularly the detailed requirements...
Posted 4/12/2011 3:12:41 PM
Misbranded Dietary Supplements and Functional Foods: Critical Updates on 2011 Enforcement Subject: Although the enforcement of the misbranding regulations applicable to dietary...
Posted 4/13/2011 9:24:22 AM
Navigating Reporting Requirements on Clinicaltrials.gov: What You Need to Know Subject: You know that you must register your studies on clinicaltrials.gov. But you...
Posted 4/13/2011 9:31:30 AM
Medical Device Design Update Requirements: Present and Future FDA Expectations Subject: Device manufacturers usually understand the requirements for a new design;...
Posted 4/13/2011 9:39:57 AM
Key GMP Systems in Pharmaceutical and Biotech Labs Subject: The FDA has ramped up surveillance and we have seen an increase in the number...
Posted 5/23/2011 1:28:50 PM
Best Practices for Managing Export Control & Cargo Claims Subject: During this two day course you will master the basics elements of U.S. export...
Posted 1/17/2012 10:09:36 AM
Foreign Clinical Trials: A Shifting Ethical Landscape Subject: As more and more clinical trials are done overseas, there are countless ethical...
Posted 6/14/2011 2:03:08 PM
Adverse Event Reporting for Medical Devices: New Enforcement Challenges Subject: Adverse event reporting is an increasing concern for medical device manufacturers,...
Posted 7/11/2011 10:53:25 AM

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