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How to Monitor Pharmaceutical, Biologic & Medical Device Clinical Trials for GCP Compliance

Posted on Jul 18, 2013 2:25:00 AM

How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance

Training Course - Los Angeles, CA, United States

This training course provides a solid understanding of GCP requirements and a clinical compliance overview for clinical trials. Attendees will gain experience in proven techniques for detecting, correcting and preventing clinical study deficiencies at domestic and international clinical sites. This course teaches you how to ensure that your data and supporting documentation are completely accurate, factual and in the appropriate format for company and regulatory authorities. Included in the course work are practical examples and a roadmap for evaluating SOPs, consent forms, investigator brochures and source documents through presentation and interactive case studies.

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(Courtesy of Hilton Los Angeles Airport (CA), via tripadvisor.com)

How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance

Mon, Jul 22, 2013 - Tue, Jul 23, 2013

The Hilton Los Angeles Airport (LAX)

5711 West Century Blvd., Los Angeles, CA 90045, United States

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Tags: CA, 2013, Medical Device Technology, Los Angeles, July, US, Development, clinical trials, Life Sciences, biotech

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