1st January, 1970


CRFWEB by CLINDOX: Proven Specialists in the MedTech eClinical Sector

The CLINDOX team’s focus and experience in medical device investigations means our CRFWEB eClinical platform provides all the tools you’ll need to support your trial program.
All your Compliance and regulatory requirements supported: FDA (CDRH) 21CFR 807 and 814, GDPR, HIPAA, MEDDEV and the transition to MDR and IVDR

The features you need, all integrated: Researcher or subject-led data capture via browser or App – ePRO – Medical coding (MedDRA) – SDV – Integrated Randomization – Trial Supply Management. MedTech specific features: Randomization for MedTech studies plus medical device log templates: AE, ADE, SAE, SADE, USADE.


Arena’s business-to-business events offer a myriad of opportunities for sponsors and exhibitors to drive their businesses forward.
Our sponsorship packages help companies educate ther target market on key industry issues and spread brand awareness throughout the

If you want to discuss how we can help you generate leads and add-value to your corporate and brand image please contact:

Paul Adams
+44 (0)20 7936 6948

Speaker opportunities

We identify and invite individuals we believe to be the best speakers in the market, if you think you can make a difference to the quality of our events please contact:

Chloe Roberts
T: +44 (0)207 936 6822