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Training on Current ICH GCP Guidelines


Wednesday, February 6, 2013 from 10:00 AM to 11:00 AM (PST)

Palo Alto, CA

Training on Current ICH GCP Guidelines

Ticket Information

Ticket Type Sales End Price Fee Quantity
Online Registration Ended $199.00 $11.94

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Event Details

This webinar on ICH GCP guidelines will offer basic ICH GCP training for all health care professionals involved in clinical research.

Why Should You Attend:

All healthcare professional involved in the conduct of clinical research must have evidence of current ICH GCP training. Regulatory agencies in most countries require that all personnel involved in clinical research must have ICH GCP training and Sponsors will not place a study at a site until it can be proven that key personnel have the required training.

This webinar is designed to offer documentation of ICH GCP training required by regulatory agencies and sponsors with minimal commitment from the participant.

Areas Covered in the Webinar:

The focus of this webinar will be on providing the basic training required to meet the needs of busy healthcare professionals. There will be documentation of completion supplied to the participant for filing in the site regulatory/training binder. The webinar will include the following critical information you will need:

  1. Background information on the need for standardized GCP guidelines for the clinical research industry.
  2. Coverage of ICH requirements for the Investigator, the sponsor and IRBs.
  3. Informed consent.
  4. Subject rights
  5. What is an adverse event?
  6. What is an essential document?
  7. Retention requirements.


For Registration:

Have questions about Training on Current ICH GCP Guidelines? Contact ComplianceOnline

When & Where

Online Webinar
2600 E. Bayshore Road
Palo Alto, CA 94303

Wednesday, February 6, 2013 from 10:00 AM to 11:00 AM (PST)

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