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DID Remarket Clinical Safety Training Course #12558 26-27 April 2012 Radisson Blu Aaron Hotel, Prague, Czech Republic Faculty Course Overview Dr. Jan Retrace CEO, Consultant, PharmInvent, Czech Republic
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What is dia premarketing clinical safety?
Dia premarketing clinical safety is the process of evaluating and ensuring the safety of a drug before it is marketed.
Who is required to file dia premarketing clinical safety?
Pharmaceutical companies are required to file dia premarketing clinical safety.
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Dia premarketing clinical safety is filled out by submitting detailed safety data and analysis of a drug.
What is the purpose of dia premarketing clinical safety?
The purpose of dia premarketing clinical safety is to evaluate the safety profile of a drug before it is marketed to the public.
What information must be reported on dia premarketing clinical safety?
Information that must be reported on dia premarketing clinical safety includes adverse reactions, side effects, and safety data.
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