Our commitment as an EDC vendor – here’s what you get

The Viedoc EDC system is designed to come with all the required and requested features of the clinical trials industry. Evaluating everything that Viedoc is capable of as well as its regulatory compliance can take a lot of time and work – time we’d rather see our clients spend on their clinical trials instead.

So, to streamline and simplify the evaluation and auditing process for both our current and future clients, we have created the Viedoc Product Specification. In this document, all the features that we commit to deliver are outlined, detailed, and explained.

Here is a selection of the features included in the Viedoc Product Specification, you can view the full specification in our new brochure:

• An electronic data capture interface to collect CRF data in an ICH GCP compliant manner.
• Regulatory compliance with clinical trial regulations according to FDA, EMA, JPMA and CFDA.
• Regulatory compliance with the Personal Data Protection laws including GDPR (EU), APPI (Japan), HIPAA (US) and the Personal Information Security Specification (China).
• A medical coding feature that supports MedDRA, WHODrug, ATC and Iyakuhinmei Data File (IDF).

Download the full product specification here.