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:
+44 (0)20 7936 6948