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La European regulation of health products established a new regulatory framework that guarantees a high level of safety and health protection for patients and users. Although this regulation is directly applicable to all countries of the European Union, there are several aspects that are left to the regulation of each Member State. In Spain, in March of this year the new Royal Decree on Health Products.
Fernando Atienza, founder of PS Consulting and expert in Medical Device Regulation, will offer the webinar "Health product: new challenges and paradigm shift", within the framework of III Cycle of Scientific Conferences from the Parc Taulí Research and Innovation Institute. Atienza will give us all the keys to this new Spanish regulation what applies to development of a health product.
Addressed to:
- Research and innovative personnel; members of Research Ethics Committees (CEI) and Medicines Research Ethics Committees (CEIm), lawyers
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