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Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
Brand Differentiation in Medical Devices Industry – Leveraging Perceptual Maps to enhance your brand positioning
Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
A Guide to EU MDR 745/2017
Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
Power of Real-World Evidence in the MedTech Industry
Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
Long-term clinical data is essential for understanding the performance, safety, and overall effectiveness of medical devices over an extended period.
ISO 14155, titled ‘Clinical investigation of medical devices for human subjects — Good clinical practice,’ while primarily known for guiding
Market research and insights are essential for driving AI adoption, providing the knowledge needed to make informed decisions, develop tailored
Market research and insights are essential for driving AI adoption, providing the knowledge needed to make informed decisions, develop tailored
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Introduction: In the dynamic arena of medical device regulation, clinical evaluations play a pivotal role in assessing the medical devices’

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In recent times collection of real-world evidence has gathered everyone’s focus and poses great potential to provide valuable insight into
In recent times collection of real-world evidence has gathered everyone’s focus and poses great potential to provide valuable insight into
In recent times collection of real-world evidence has gathered everyone’s focus and poses great potential to provide valuable insight into
The convergence of proactive and reactive methodologies within a post-marketing surveillance (PMS) system can significantly enhance the effectiveness and robustness
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‘Sufficient clinical data’ is a critical term used in the context of medical device regulations to describe the level of
How can an EU MDR certificate can open doors to other markets?
The EU Medical Device Regulation (MDR) is a set of regulations that govern the safety and performance of medical devices
Doctors wearing VR simulation with hologram medical technology
Medtech companies are expected to play a key role in the digital transformation of healthcare. Many are already prioritizing building
PMPF Surveys for IVD Products

Introduction: As the regulatory environment progresses, ensuring the safety, performance, and compliance of In Vitro Diagnostic (IVD) products is of

Guideline to Perform Conformity Assessment for Medical Devices in Europe under the EU MDR 2017/745

Introduction: The European Union Medical Device Regulation 2017/745 (EU MDR) has brought significant changes to the regulatory landscape for medical devices

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In the rapidly evolving landscape of medical devices, ensuring patient safety and product effectiveness is of paramount importance. Post-Market Clinical

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The fusion of market research and regulatory considerations can provide valuable insights and help medical device manufacturers make informed decisions

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MedTech product managers often use Customer Insights or Voice-of-Customer analysis to gain market insights and make evidence-based decisions for their

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