Date :
Place : United States, Fremont
Contact Person:OCP Panel
Description:
Join this webinar to review FDA recommendations on the use of Electronic Health Records (EHR) in FDA Regulated Clinical Investigations. Register Today.Deadline for abstracts/proposals : 14th June 2017
Organized By :Online Compliance Panel
Keynote Speakers : Rachelle D'Souza has licensed various medical and consumer products and facilities for start-ups and multi-national companies. Her expertise also includes clinical trial master file documentation, and the design and maintenance of globally compliant quality, safety/pharmacovigilance and medical information systems At Regulatory Heights Inc., Rachelle continuously monitors the current regulatory environment and utilizes regulatory intelligence as a strategic business driver for her client
Conference Highlights :This training includes FDA's current recommendations on the use of Electronic Health Records (EHR) in clinical investigations and a refresher on key requirements for Computer Systems used in Clinical Investigations. Check out the key learning objectives and specific areas covered in this context. If you are a sponsor of a clinical trial involving a drug, biologic, medical device or combination product, a clinical investigator, a Contract Research Organization (CRO) or an Institutional Revie
Venue :United States
Check the event website for more details.