On 13 July 2021 at 11.00 am, Gabinete Técnico Farmacéutico M. Camps and the Medifocs team will be hosting a webinar on the role of the person responsible for regulatory compliance for medical devices.
Following the entry into force of the new Regulation (EC) No 2017/745, which sets out in Article 15 the duties and obligations of the Compliance Officer, the medical devices market is still in the process of adapting to the new European regulations. Among other issues, one of the most frequently raised concerns amongst medical devices companies relates to the role of the Compliance Officer.
Through the webinar «The Person Responsible for Compliance with Medical Device Regulations: Obligations, Responsibilities, Tasks and Competences. How to interpret Article 15 of Regulation (EU) 2017/745«, you’ll be able to get answers to your questions about the role of the Data Controller from the experts at GTF M. Camps and Medifocs.
Are you interested in taking part in the webinar? Follow this link:
Further information about the webinar
Recipients: Aimed at professionals working in organisations within the medical devices supply chain (including manufacturers, agents, distributors, importers and producers).
Aim of the training: To provide information and clarification on the role of the person responsible for regulatory compliance under Article 15 of Regulation (EU) 2017/745. During the meeting, there will be an opportunity to ask specific questions on the subject in order to gain a better understanding.
Speakers: Fabio Tommasi Rosso
Moderation: Mercè Camps