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Medical Devices in Europe under the EU MDR 2017/745, A Quick Guideline to Perform Conformity
Master EU MDR conformity assessment for medical devices: classification, assessment routes, documentation, and post-market obligations for compliance.
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Discover how PMCF surveys revolutionize data collection for legacy medical devices. Ensure regulatory compliance and improve patient outcomes effectively.
Market Research and Regulatory Considerations Drive Informed Decisions for Medical Device, PMPF Surveys for IVDR
How integrating market research and regulatory insights empowers medical device manufacturers to make informed decisions and achieve successful market launches.
Market Research, MedTech Product, Clinical and Regulatory Services
Discover key market research studies for MedTech product managers: Customer Insights, Conjoint Analysis, Market Sizing, Unmet Needs, Concept Testing.

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