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OPTIMARC was pleased to participate in the 13th Clinical Research Day, an essential event for exchanging information on advances, best practices and the future of clinical research in France.

Optimarc offers you a new website . You will find under the different sections our knowledge, our experiences, our trainings....Thus we can guarantee quality services to conduct your trials in the best way. We will offer you a budget adjusted to your study with CRAs located closely to your investigative sites. You will find our contact details under section "contact". Enjoy your navigation on our new website!

This year, the beautiful city of Lyon was chosen as the venue for the Optimarc Association's Annual Meeting 2024. It was an opportunity for the CRAs to get together for a day of exchanges and to elect the new board, whose composition can be found on the “contact” page of our website. We look forward to hearing from you!

A half-day of interactive training including a practical part to: - Understand and recall the framework of European Regulation 536/2014 governing the conduct of clinical trials of medicinal products - Understand the general operating principles of the CTIS platform - Be able to anticipate the submission of clinical trials under the new regulation A big thank you to our trainer Yvain Robreau for his high-quality presentation!

Once again this year, Optimarc attended the AFCROs Clinical Research Day. It was a great opportunity for our CRAs to network and take part in the various workshops offered. Our CRAs were able to participate in the following sessions: Developing the key elements of a study with patient associations Decentralized Clinical Trials AI and Clinical Research It was a valuable moment of sharing and discussion, held this year in a new venue: Rive Montparnasse in Paris. A smaller s

The programme in brief : 1. European Regulation EU-2017/745 o Origin and principles of medical device regulation o Legislative developments and timetables o The new ‘product’ scope and classification criteria o The status of economic operators and their new responsibilities 2. CE marking o Conformity assessment procedures o The new general performance and safety requirements o Focus on clinical evaluation o Traceability and information - patient information - UDI and Eudamed

A look back at the Optimarc Association's General Meeting 2023 in Porto! An opportunity for our independent CRAs to get together and exchange ideas with their peers.

The OPTIMARC association was on hand for the 11th AFCROs Day! With its stand, this day was rich in meetings with professionals and actors in Clinical Research. Participation to the workshops also provided an opportunity to discuss the latest developments in clinical research, as well as common problems encountered:  1 - European Medicines Regulation: 1-year review2 - Early and compassionate access3 - EUCROF's GDPR code of conduct4 - BNDMR: a new tool for the production of rea