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Often the greatest challenge in getting a medical
product approved is first defining its actual requirements. Retlif
can assist in the effort, especially through our Washington
Regulatory office, which can interface with the
FDA and other agencies on your behalf. Once
the requirements are defined, we can help you to develop a comprehensive, yet cost
effective, testing program, which will assure acceptance of your product.
Program Management
Further, customers often find the compliance process to be a complex, time-consuming effort and may not have the in-house staff to address it. Our Engineering Services Division manages the entire compliance program. Services such as interfacing with your customer and regulatory officials, defining testing programs, overseeing the testing and final compliance documentation can all be provided.
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