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34594 Conferences

SOPs for Clinical Trials – Regulatory Requirement and Key to Effective Management

Added by Referral on 2012-01-05

Conference Dates:

Start Date Start Date: 2012-01-19
Last Date Last Day: 2012-01-19

Conference Contact Info:

Contact Person Contact Person: Referral
Email Email:
Address Address: 2600 E. Bayshore Road, Palo Alto, California, 94303, United States
Phone Tel: +1-650-620-3915
Phone Fax: +1-650-963-2556

Conference Description:

This SOPs for Clinical Trials training will cover ICH-GCP and ISO 14155 requirements for SOPs. It will outline steps to effectively develop and maintain SOPs and manage risks to your clnical research operation, through their use.

Why Should You Attend:

Failure to establish, maintain and adhere to written SOPs for Clinical Trials, expose the organization to Regulatory actions. These actions include, but are not limited to, seizure, injunction and/or civil money penalties and might even result in project/s discontinuation.

SOPs that are not appropriately written might bear risks due to: deviations, use of unauthorized versions/copies, misinterpretation, non-acceptance, lack of availability and more.

This training will show how you can write effective SOPs that will benefit the organization’s clinical research operations and general management by ensuring quality, efficiency, compliance with applicable requirements, reliability, consistency, accountability, process control, proper internal communication, change implementation, conservation and controlled distribution of knowledge and more.

For Registration: rce/control/trainingFocus/~product_id=70 2179?channel=worldconf
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