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The Differences Between Clinical and Post Market Medical Reviews
This Webinar is over| Date | Mar 30, 2016 |
| Time | 10:00 AM EDT |
| Cost | Free |
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Online
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There are two major categories of safety monitoring: “Clinical” which refers to safety monitoring of clinical trials and “Post-marketing”, safety monitoring of situations following approval and marketing, other than directly associated with clinical trials.
For both scenarios, monitoring consists of four basic elements: receiving safety information; processing and recording information; reviewing and analysing information; and, lastly, acting upon information. The good safety medical reviewer is involved in all aspects of the safety cycle, although the level of involvement, and the specific tasks, may vary, depending on whether the scenario is clinical or post-marketing.In this webinar, learn about the differences between clinical and post market medical reviews.
Speaker: Margaret McCulloch, M.D. , Medical Doctor, Ashfield Pharmacovigilance
For both scenarios, monitoring consists of four basic elements: receiving safety information; processing and recording information; reviewing and analysing information; and, lastly, acting upon information. The good safety medical reviewer is involved in all aspects of the safety cycle, although the level of involvement, and the specific tasks, may vary, depending on whether the scenario is clinical or post-marketing.In this webinar, learn about the differences between clinical and post market medical reviews.
Speaker: Margaret McCulloch, M.D. , Medical Doctor, Ashfield Pharmacovigilance
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