Latest From Cetas Healthcare

MedTech devices and diagnostics, Power of Real-World Evidence
Explore how real-world evidence (RWE) impacts MedTech: clinical trials, post-market surveillance, and health economics. Discover challenges and opportunities.
Diagnostic (IVD) devices - post-market surveillance (PMS) for In Vitro
Post-market surveillance (PMS) strategies for in vitro diagnostic (IVD) devices. Ensure regulatory compliance and enhance device safety and performance.
Clinical Surveys for Monitoring Medical Device
Explore how long-term clinical surveys monitor medical device safety, performance trends, patient outcomes, and regulatory compliance with Cetas Healthcare
MedTech Market Signals With Brand tracking
Discover how brand tracking enhances MedTech market strategies. Evaluate brand perception, adapt to market dynamics, and attract investments effectively.
Guiding Principles of ISO 14155 for Post-Market Clinical Follow-up (PMCF) Surveys for Medical Devices
How ISO 14155 shapes PMCF surveys for medical devices. Learn from Cetas Healthcare's expertise in post-market clinical follow-up and regulatory compliance.
Post-Market Clinical Follow-up (PMCF) surveys - medical devices, Crafting an Effective PMCF Survey
Essential tips for crafting effective PMCF surveys. Ensure your medical device surveys yield reliable data with structured design and execution strategies.
Market research, MedTech and Artificial Intelligence (AI) in Healthcare
Market research & insights effectively are better equipped to seize the growing AI opportunities, mitigate risks, and drive successful AI adoption initiatives.

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