THIS WEBINAR WILL DISCUSS FDA’S CURRENT RECOMMENDA 2007 - Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations -By Compliance Global Inc

Website http://bit.ly/2rPnvPU | Edit Freely

Category fda capa training, fda training, fda system validation, clinical trial tmf, clinical research training, ehr incentive program, electronic health record data, training log template, clinical investigations, fda alcoa guidance, emr training, emr systems in healthcare

Deadline: July 05, 2007 | Date: July 05, 2007

Venue/Country: Online, U.S.A

Updated: 2017-06-09 15:41:56 (GMT+9)

Call For Papers - CFP

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 review board (IRB), you stand to benefit from this training.

Why Should You Attend:

Did you know that electronic health record (EHR) can be used in prospective clinical investigations of human drugs, biologics, medical devices and combination products regulated by the US Food and Drug Administration (FDA)? This includes foreign studies used in support of an application for marketing approval of the medical product.

Areas Covered in this Webinar:

FDA Recommendations on

Whether and how to use EHRs as a source of data in clinical investigations

Using EHRs that are interoperable with electronic systems supporting clinical investigations

Ensuring the quality and integrity of EHR data that are collected and used as electronic source data in clinical investigations

Learning Objectives:

Ensuring that the use of EHR data collected and used as electronic source data in clinical investigations meets FDA’s inspection, record keeping and record retention requirements

Who Will Benefit:

Sponsors of clinical trials (drug, biologic, medical device & combination product manufacturers)

Clinical Investigators (physicians)

Contract Research Organizations (CROs)

Institutional Review Boards (IRB) / Ethics Review Boards (ERB) / Research Ethics Boards (REB)

For more information, please visit : http://bit.ly/2rPnvPU

Email: supportcomplianceglobal.us

Toll Free: +1-844-746-4244

Tel: +1-516-900-5515

Speaker Profile:

Rachelle D’Souza, CEO of Regulatory Heights Inc., has successfully licensed various medical and consumer products and facilities with international regulatory authorities / agencies for multinational and start-up 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 clientele. Her numerous articles on the latest international regulatory developments have been published in print and on-line by regulatory professional associations and industry magazines around the world.

Her versatility has enabled Regulatory Heights Inc. to support companies, in particular, start-ups with the licensing of their drugs and medical devices in international markets.