The European Economic Area (EEA), inclusive of the European Union (EU) and European Free Trade Association (EFTA), has been contemplated as one of the largest global medical device markets. The obvious aspiration for device manufacturers is gaining an approval and maintaining access to this important market. It requires abiding by the regulatory changes to assure timely product certification. The white paper describes an approach on implementation of new EU medical device regulation (EU MDR) for medical device manufacturers. The approach is developed by considering the impacts to key changes in regulations and implementation practices for the industry.
Need for Ethical Guidelines Presentation and interpretation of clinical data purely depends on authors and presenters. The entire research is usually
What is Plagiarism? The word plagiarism has been derived from the Latin word “plagiarius” meaning “kidnapper” or “abductor” [1]. Plagiarism may
The medical device industry is undergoing a surge in growth, with new products being developed andintroduced into the market to
The 21st century has witnessed a breakthrough in the field of healthcare. Technology in healthcare has taken a giant leap
Technological advancements progress through cycles of disruption and gradual change. Communication has continuously evolved, from the printing press to modern
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