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CRC Cardiogenic Shock Lean CRF: V4 Followup Form & Secondary Components NOT FOR USE WITHOUT PERMISSION. 2022Follow Up Assessment after Shock Onset (For serial entry, use the time period from the last
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Who needs cardiac safety research consortium?

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Pharmaceutical companies conducting clinical trials that involve testing the cardiac safety of new drugs.
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Research institutions or organizations studying the effects of certain treatments on the heart.
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Regulatory agencies overseeing drug approval processes and safety monitoring.
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The Cardiac Safety Research Consortium (CSRC) is a public-private partnership that aims to facilitate the efficient and effective development of new cardiac safety assessment approaches for new medical products.
Researchers, sponsors, and regulatory agencies involved in the development of new medical products are typically required to file cardiac safety research consortium.
To fill out the cardiac safety research consortium, researchers and sponsors must provide detailed information on the cardiac safety assessments conducted during the development of new medical products.
The purpose of the cardiac safety research consortium is to improve the assessment of cardiac safety for new medical products and ensure patient safety during clinical trials and post-market surveillance.
Information on the design of cardiac safety assessments, study results, and any cardiac safety issues encountered during the development of new medical products must be reported on the cardiac safety research consortium.
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