Latest From Cetas Healthcare

Cardiovascular Care: A MedTech Market Research Perspective

Decoding Patient Journeys in Cardiovascular Care: A MedTech Market Research Perspective

Introduction: Cardiovascular care is advancing rapidly, driven by innovations that aim to transform patient experiences and outcomes. At the forefront of this transformation are the detailed patient journeys—from the first signs of symptoms to long-term

Qualitative insights and Market analysis - MedTech

Introduction: “How likely is it that you would recommend our company/product/service to a friend or colleague?” One simple question that provides a clear line of sight into the company’s customer relationship landscape. The strengths are

EU Medical Device Regulation (MDR) Insights for MedTech

Introduction: As we navigate through critical regulatory milestones in the medical device industry, it is essential for manufacturers to fully understand the impact and requirements of the EU Medical Device Regulation (MDR). With pivotal compliance

Customer Segmentation is Vital for Medical Device Manufacturers

Introduction: In the intricate realm of medical device manufacturing, success hinges upon a deep understanding of the diverse needs and preferences of healthcare professionals, institutions, and end-users. Customer segmentation emerges as a critical tool in

Market Research Studies for Medical Device

Introduction: In the dynamic and rigorously regulated medical device industry, the introduction of a new product demands not only strategic foresight but also robust execution, underpinned by a thorough understanding of market needs, customer expectations,

MedTech Market - Medical Technology

Introduction: In a crowded MedTech marketplace, how do you stand out? While each brand is contesting for the attention and trust of customers, including healthcare providers, patients, and purchasing decision-makers – how do you communicate

Medical Devices – MedTech Market

Introduction: Once upon a time, MedTech companies could afford to be sales driven organizations on the back of their engineering prowess. Alas, those days are now over. MedTech companies face a consistent challenge of distinguishing

European Medical Device Regulation (EU MDR 745/2017)

Introduction: The European Medical Device Regulation (EU MDR 745/2017) has significantly enhanced the regulatory framework governing medical devices in the European Union (EU). Among its many provisions, incident reporting stands out as a crucial aspect

We provide the best insights for your business