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Use of Excel Spreadsheets in FDA-Regulated Environments under 21 CFR Part 11
Why you should attend: This seminar will provide great opportunities to improve our awareness an..

Live Session By Dr. David Lim On Wednesday 21st of August 2019 10:00 AM PDT | 01:00 PM EDT
$195.00
FDA 510(k): Preparation, Submission, and Clearance Medical Devices
This webinar is intended to discuss regulatory requirements for FDA 510(k)s: in particular, 510K) pr..

Live Session By Dr. David Lim On Wednesday 21st of August 2019 11:00 AM PDT | 02:00 PM EDT
$195.00
Risk Analysis and Risk Mitigation
Goals The specifications usually miss about 60% requirements. Therefore risk risks are inherent i..

Live Session By Dev Raheja On Friday 6th of September 2019 10:00 AM PDT | 01:00 PM EDT
$195.00
Fundamentals of Regulatory Affairs in Human Drugs
Why you should attend:      To understand and become familiar with the Fundame..

Live Session By Dr. David Lim On Friday 13th of September 2019 10:00 AM PDT | 01:00 PM EDT
$195.00
CAPA Training and Causes of Warning Letters due to Lack of Comprehension
A timely, well documented, Corrective / Preventive Action program validates a quality system that is..

Live Session By Jerry Dalfors On Friday 20th of September 2019 10:00 AM PDT | 01:00 PM EDT
$195.00
Best Practices for FDA Inspection Preparation and Management
This webinar is intended to help you get familiar with the best practices for FDA inspection prepara..

Live Session By Dr. David Lim On Friday 27th of September 2019 10:00 AM PDT | 01:00 PM EDT
$195.00
Medical Device Reporting (MDR)
Description of the topic: Manufacturers of Medical Devices are required to report to the FDA when..

Live Session By Jerry Dalfors On Friday 4th of October 2019 10:00 AM PDT | 01:00 PM EDT
$195.00
Designing a Good Medical Device
Goals Designing a good medical device is an art as well as science. Engineering 101 sciences say ..

Live Session By Dev Raheja On Thursday 17th of October 2019 10:00 AM PDT | 01:00 PM EDT
$195.00