Global Market Research

Gathering all regulatory market data at the earliest stages of your product development will help you identify and address potential impacts to your design. With our market research services, we can help to facilitate a smooth transition to testing, and ultimately a faster, less complicated certification process for you and your business.

• Identify local country requirements specific to your product
• Develop a customized regulatory strategy based on your priorities

** The Intertek legal entities that provide medical device management system certification services (including ISO 13485 and MDSAP) and Notified Body services (MDR 2017/745 and MDD 93/42/EEC) do not provide any consulting services. Clients who have used other Intertek legal entities’ consulting services are not eligible to receive management system certification services or Notified Body services from Intertek.