Latest From Cetas Healthcare

Post-market clinical follow-up (PMCF), PMCF, Orthopaedic devices, Medical Device Regulation, MDR, Clinical evidence, Regulatory requirements, High-risk devices, Regulatory complexity, Compliance, Clinical data, Legacy devices
Explore the challenges of designing & conducting PMCF studies for orthopaedic devices under MDR, focusing on compliance, clinical evidence, and data collection.
As healthcare systems across Europe continue to evolve, the demand for advanced imaging technologies—such as ultrasound, MRI, CT scans, and AI-driven imaging tools—remains strong.
Message Online Chat Social Text Concept, Message Testing in Orthopedics
The journey of a medical device extends far beyond its launch. And post-market clinical surveys emerge as a pivotal tool, not only in sustaining the lifecycle of medical devices but also enhancing their safety, efficacy,
Market Landscape, Decision-Making Process, Opportunities in Glaucoma Care
Key opportunities in glaucoma care for MedTech innovators in the EU. This market overview highlights treatment trends, and strategic insights for driving innovation in glaucoma management.
Life Science, Brand Health Tracking (BHT), The Power of Brand Health Tracking
Life science companies can gain a competitive edge through Brand Health Tracking. Continuous monitoring of brand performance boosts trust, reputation, and innovation.
Transforming Diagnostic Imaging
The journey of a medical device extends far beyond its launch. And post-market clinical surveys emerge as a pivotal tool, not only in sustaining the lifecycle of medical devices but also enhancing their safety, efficacy,
Remote Monitoring in Healthcare

Introduction: In today’s healthcare landscape, remote monitoring stands as a pivotal innovation transforming how patient care is delivered. By leveraging technology, healthcare providers can monitor patients outside traditional clinical settings, enabling continuous care and early

KOLs Drive Innovation & Adoption in Medical Devices

Introduction: Key Opinion Leaders (KOLs) play a crucial role in the medical device industry. Their expertise, influence, and ability to bridge the gap between innovation and clinical practice make them invaluable in driving both the

MedTech devices, Crafting Detailed PMS Plans for Orthopae
Over my 13 years as a regulatory professional, I've seen firsthand just how crucial Post-Market Surveillance (PMS) plans are, especially for specialized MedTech devices like those in orthopaedics.

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