Services.Commercially successful medical devices are founded on early and continuous regulatory compliance planning to design and factor regulatory requirements into the final product. MedReg works with clients to provide critical insight on activities and methods necessary to ensure that devices demonstrate safety via objective scientific evidence and pass expediently through regulatory submission and registration activities.
|
We Promise Quality and Satisfaction.
Regulatory AffairsMedReg Consulting is your one-stop shop for early due diligence research and reporting though design, testing, submission, and approval for commercial sale in target markets.
MedReg will map and complete RA deliverables for the client enabling them to focus their resources on innovations in science to promote medical product services and technologies that improve the lives of patients worldwide. Services and Experience
|
Clinical/Medical AffairsMedReg partners with clinical experts at Medicore International, Inc. to plan, implement, and effectively meet clinical activity requirements to provide clients with reliable safety data through streamlined business activities.
Working with Medicore International, MedReg will ensure that clinical strategies meet regulatory requirements and manage all aspects of clinical validation. Services and Experience
|