There is a clear need for a CRO who understands the needs and limitations of dental manufacturer and is able to provide sites with the necessary ancillary resources to complete complicated trials.
ECLEVAR has extensive experience with dental devices and in offering the most cost-efficient, timely contract research organization (CRO) services for these types of organizations.
Our expertise : (non-exhaustive list)
Regulatory requirements and compliance for dental devices are covered under the Medical Devices reglementation. As an experienced CRO, we have a unique skill-set to help you reach european markets faster. Our consultants have conducted beneficial gap analyses and audits for many dentals’ companies
Twelve (12) months ago, the EU Commission published a Notice to Stakeholders, “Withdrawal of the United Kingdom and EU Rules in the Field of Industrial Products,”Read More..
ECLEVAR invites you to meet with us at MedTec Japan in Tokyo, Japan on 18-20 April.