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The objective of this course is to provide an overview of the preparation, design and management aspects of clinical trials for medical devices. Upon completion of this course, attendees will have an understanding of the unique challenges faced in clinical...
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This two-day course has been designed as an introductory course on the Quality System Regulation (QSR) for medical device and biotech personnel. It will assist those who are responsible for compliance with FDA QSR requirements. The seminar is particularly...
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This two-day course is designed for those involved with Clinical Research, Safety Surveillance, Regulatory Affairs, Clinical Trials, Medical Affairs and QA/QC issues. It will also benefit Audit personnel and those in management who require a full understanding...
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This two-day course will be most valuable to medical device software engineers, engineering managers, scientists, and quality engineers (particularly in product development). This course will also be of benefit to quality assurance and regulatory affairs...
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This two-day course was developed to assist personnel who have varying levels of experience in drug and device advertising, marketing and promotion. It is intended for those involved with: Read More...
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This course is an overview designed for those in the Pharmaceutical, Biotech and Medical Device industries who will manage or direct projects within their functional area related to Clinical Trials. It will also benefit those who need an understanding...
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This course will provide value to those in the Pharmaceutical, Biotech and Medical Device industries who manage or direct projects within their functional area related to Clinical Trials. It will also benefit personnel that need an understanding of industry...
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