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PJ.AFFIDAVIT OF PUBLICATIONSTATE OF KANSAS, RICE COUNTY, SSV Daniel B. Marshall being first duly sworn, deposes and says ', 'hat he is publisher of THE STERLING KANSAS BULLETIN A weekly newspaper

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What is cdr - r?

CDR-R stands for Clinical Data Request - Reporting, which is a document filed by pharmaceutical and medical device companies to report clinical trial data to regulatory bodies.

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Pharmaceutical companies, biotech firms, and medical device manufacturers who conduct clinical trials and wish to market their products are required to file CDR-R.

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To fill out CDR-R, companies must provide detailed information about the clinical trials, including study design, results, and statistical analysis. Specific guidelines can usually be found on the regulatory agency's website.

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The purpose of CDR-R is to ensure transparency in clinical trial data, facilitate regulatory review, and uphold public trust in the safety and efficacy of medical products.

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Reported information must include trial protocol, study outcomes, statistical methods used, adverse events, and demographic information about participants.

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