The Why, How, When And What Of EU MDR Regulation

With the European Union's Medical Devices Regulation now in full effect, manufacturers face the imperative task of comprehending and adhering to its stipulations. Manufacturers must ascertain their readiness to meet the requirements, evaluate the impact of reclassification on their products, engage with notified bodies, and stay abreast of ongoing developments.

Gain invaluable insights into navigating the nuances of the Medical Devices Regulation by tuning in to the PharmaLex podcast below, featuring expert analysis from Jean Boudaud. With extensive experience spanning all phases of the product lifecycle, Jean brings valuable Regulatory and Quality Assurance expertise to diverse companies, ranging from start-ups to multinational corporations. His bilingual proficiency in French and English, coupled with a Masters' Degree of Engineering (MEng.), positions him as a trusted resource in guiding companies through the complexities of regulatory compliance in the medical devices industry.