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It aims to help with defining study populations and designing study protocols For a complete list of scientific guidelines currently open for consultation, see public consultations. It provides guidance on data collection, data quality management and data analysis to achieve higher quality evidence

The guideline focuses on studies. A total of 61 research. Read on for our take on the draft guideline issued in september 2020

The ema has now issued the final guideline dated 22 october 2021, confirming the agency’s interest in using patient registries (prs) for pharmacoepidemiologic safety and effectiveness research [2].

The study followed the strobe reporting guideline All eligibility criteria, keyword terms, and extracted variables are summarized in the figure. The european medicines agency (ema) has published new guidance on generating evidence from patient registries The publication aims to increase the quality of research using the wealth of data available from disease registries

Patient registries collect uniform data over time on patients who are diagnosed with a particular disease or condition, or who receive particular medicines

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