As clinical trials are conducted, inspections ensure quality and integrity of care, data and drug performance. As sponsors for clinical trials, pharmaceutical companies are required to ensure GCP guidelines are upheld by implementing inspection readiness. These inspections are conducted by regulatory authorities, which all have unique regulations and caveats. These nuances make inspection readiness a difficult and resource-consuming battle. Clinical trials must be prepared for visits from countless stakeholders over their course.

Date : 7th August 2017 to 8th August 2017

Place : United States, Philadelphia

Website :https://www.eventbrite.com/e/6th-clinical-trials-inspection-readiness-summit-exl-tickets-34260761861?aff=NDT

Contact Person:Paula Edwards

Description:

As clinical trials are conducted, inspections ensure quality and integrity of care, data and drug performance. As sponsors for clinical trials, pharmaceutical companies are required to ensure GCP guidelines are upheld by implementing inspection readiness. These inspections are conducted by regulatory authorities, which all have unique regulations and caveats. These nuances make inspection readiness a difficult and resource-consuming battle. Clinical trials must be prepared for visits from countless stakeholders over their course.

As clinical trials are conducted, inspections ensure quality and integrity of care, data and drug performance. As sponsors for clinical trials, pharmaceutical companies are required to ensure GCP guidelines are upheld by implementing inspection readiness. These inspections are conducted by regulatory authorities, which all have unique regulations and caveats. These nuances make inspection readiness a difficult and resource-consuming battle. Clinical trials must be prepared for visits from countless stakeholders over their course. will be held in Philadelphia,United States on date 2017-08-08

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Deadline for abstracts/proposals : 1st August 2017

Keynote Speakers :

Conference Highlights :Use different perspectives on inspection readiness to improve clinical operations and guarantee success Promote and ensure compliance with all regulatory agencies and their regulations using new systems and innovative methodologies Ensure trials are organized with improved oversight and communication to protect study participants’ rights, safety and welfare Foster the intelligent design of clinical trial inspection readiness procedures by identifying trends that improve and encourage

Venue :Philadelphia, PA 19103, United States

Check the event website for more details.