How to Comply with 21 CFR 11 Requirements

Date : 2nd May 2018 to 2nd May 2018

Place : United States, Fremont

Website :http://www.compliance4all.com/control/w_product/~product_id=501746LIVE?channel=allconferencealerts_May_2018_SEO

Contact Person:Event Manager

Description:

Overview: In this webinar would apply to computerized systems that create source documents (electronic records) that satisfy the requirements in 21 CFR 312.62(b) and 812. Areas Covered in the Session: What are source documents and why are they important? (FDA and ICH GCP E6 Guideline) What are required characteristics for source documents? What is 21 CFR Part 11? How can you apply 21 CFR 11 and ICH E6 to source documents? How EMR Data is used in Clinical investigations How to plan electronic source document deficiencies

How to Comply with 21 CFR 11 Requirements will be held in Fremont,United States on date 2018-05-02

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Deadline for abstracts/proposals : 1st May 2018

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.