Conference Details

Join this webinar to review FDA recommendations on the use of Electronic Health Records (EHR) in FDA Regulated Clinical Investigations. Register Today.

Date :

Place : United States, Fremont

Website :

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.

Join this webinar to review FDA recommendations on the use of Electronic Health Records (EHR) in FDA Regulated Clinical Investigations. Register Today. will be held in Fremont,United States on date 2017-06-15

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

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