Call for Authors & Reviewers

MDlaw is looking for Authors & Reviewers

MDlaw.eu is the most extensive information platform on MDR & IVDR. Our goal is to provide all the MDR & IVDR related information on a single platform and enable our members to safely transition and become compliant with the new medical device legislation. You can learn more about mdlaw.eu here and view this video!

MDlaw is a project powered by Obelis Group, one of the largest center in Europe for CE marking, European Authorized Representative (EC REP) EU Representative services. Obelis Group is also member of the European Association of Authorized Representatives (E.A.A.R.), EU Associations and EU Commission working groups.

We are looking for guest submissions to bring a diversity to its publications, while enriching the consistency of its content. Submissions shall be oriented towards helping the manufacturers to implement MDR & IVDR requirements through Guidance documents, templates, checklists and more. Also specific to different classes of devices or relevant for distributors/importers only.

What are we looking for:

  1. Experience and expertise in the field of MDR & IVDR,
  2. Proven track record of publishing or review is desirable,

Why you should apply:

  • MDlaw is a great opportunity for you to build your portfolio and get more eyes on your work,
  • Promotion of guest writers: we include author bio, social media profiles to generate further exposure,
  • Be part of a professional network of experts in the field of MDR & IVDR, partnership with Team-PRRC, QUNIQUE, Qmed Consulting;
  • Your text will be reviewed by independent experts and (if approved) made available for purchase on MDlaw Store;
  • Authors receive up to 25% of sold publication;
  • Reviewers are awarded with Certificate of Official MDlaw Reviewer and select from MDlaw membership or monetary compensation:

If you are interested in sending us your application, please contact us now!

Send us an email here: mdlaw@obelis.net