5.00 pm
Welcome and Introduction

5.15 pm
Regulatory Requirements for medical
devices in the pre and post market phases.

5.45 pm
Coffee Break – networking opportunity

6.00 pm
Clinical Trial Submissions to Ethics
Committees and Competent Authorities
in the European Union

6.30 pm
Market access and reimbursement of
innovative medical devices
in Switzerland and Germany

7.00 pm
Apero – networking opportunity


The importance placed on the clinical experience of medical devices is increasing. Regulatory obligations require that this is shown throughout the lifecycle of a medical device, demonstrating its safety and performance.

The evidence gathered ensures delivery of the best medical practice to healthcare providers and thereby the best care to patients.

D-Target is a specialized Contract Research Organisation (CRO) that has over 10 years experience conducting clinical investigations of both Medical and In Vitro Diagnostics Devices in all phases.


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