QUESTIONSSOPs for Clinical Trials – Regulatory Requirement and Key to Effective Management (Clinical Training)
Venue: Online Event
Location: Palo Alto, California, United States
| Event Date/Time: Jan 19, 2012 | End Date/Time: Jan 19, 2012 |
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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.
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.
