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Monday, August 13, 2018 - 8:00 AM
to Tuesday, August 14, 2018 - 5:00 PM
8:00 AM - 5:00 PM See all dates and Times
http://go.evvnt.com/220897-3?pid=2809
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With the pharmaceutical regulatory environment constantly evolving, it is extremely important to always be prepared for an inspection during a clinical trial. As sponsors of clinical trials, pharmaceutical companies are required to ensure GCP guidelines are upheld by implementing inspection readiness. Inspections are a crucial part of clinical trials, and it is extremely important that all companies are ready and properly follow GCP guidelines. Inspections are an ongoing process involving all stakeholders, and the real question is how/what can you do in your organization to reduce the frequency of inspections? By properly preparing for inspections, adopting and understanding all the requirements, and having good documentation and data management, companies will have a better chance of warding off inspections and have successful outcomes their trials.