Editor’s Note: Sanmina, a global electronics manufacturing services provider, has released the whitepaper, “Regulatory expertise accelerates time to market.” The paper describes the company’s ability to help a customer bring their product to market more quickly. A snippet of the whitepaper is presented here and the full whitepaper can be accessed here.
The medical aesthetic device market is experiencing double digit growth. Quickly launching new products to meet this demand is becoming more challenging as device manufactures face increased regulatory scrutiny. To help meet requirements, aesthetic and other medical device OEMs are partnering with EMS companies that have the knowledge of FDA filings necessary to get new products to market in a timely manner.
A developer in skin rejuvenation and aesthetic products recently developed a new laser-based treatment product but did not have the resources to develop all of the documentation necessary to support regulatory and FDA approval. To get the product to market, the company realized they needed to engage with a global EMS partner with facilities certified for medical device manufacturing and the regulatory expertise to support the successful launch of their product. They chose Sanmina.