Mediclever partners with the following expert service providers, offering business development, regulatory, quality and clinical research services:
- Donawa Lifescience Consulting - Clinical, Regulatory and Quality consultants for the medical device, IVD and pharmaceutical industries
Donawa Lifescience Consulting (DLC) is a full service CRO, working in Europe, US and Canada and a trusted partner for companies needing to meet US and EU clinical data requirements. The firm is also a recognized resource for regulatory and quality system services for medical devices, IVDs and drug-device combination products, and for EU Authorized Representative and US Agent services. The combination clinical study services together with regulatory and quality system services is very much appreciated by DLC clients. For over 20 years, DLC has helped medical device companies enter the US and EU US markets, meet US and EU quality system and post-market requirements, and maintain compliance in a pragmatic and cost-effective manner. DLC is headquartered in the historic center of Rome, Italy. Contact us for a confidential discussion about your project.
