Market Access Monitor
Service of monitoring key reimbursement and HTA developments for medical devices, in-vitro diagnostic tests, and digital technologies in Europe and globally
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MTRC has released a White Paper "Best Reporting Checklists for Studies of Medical Devices"
When designing and reporting studies of medical devices, manufacturers should follow established reporting checklists to ensure transparency, completeness, and compliance with regulatory and ethical standards. Reporting checklists ensure that studies of medical devices are conducted and documented in a transparent, reproducible, and standardized manner.
Various reporting checklists apply depending on the type of study (e.g., randomized trials, observational studies, systematic reviews, regulatory submissions). This White Paper explores the best reporting checklists for medical device studies (CONSORT, STROBE, STARD, PRISMA, PRISMA-DTA, SPIRIT, and TIDieR), their key components, and how they improve research transparency.
Read more and request a White Paper here to gain actionable insights that support the assessment of reliability, validity, and reproducibility in medical device research.