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Maven Profcon

Member since: Jul 03, 2022
Published articles: 3

Best Regulatory Consultant for US Fda 510K Approval in USA

The U.S. Food and Drug Administration (FDA) has created an online system that allows companies to apply for approval to market new medical devices. This process is called the 510(k).510k ApprovalWant...

Articles > Business & Careers > Business Services Nov 17, 2022
Why Do Companies Use Medical Device Technical Files? What Are They Used for?

A medical device technical file describes how a medical device works, what it looks like, and how it should be used. The file also includes instructions for manufacturing the device, which include...

Articles > Business & Careers > Business Services Aug 06, 2022
Why Do I Need a Medical Device Technical File?

Medical device manufacturers have to comply with strict regulations when selling their products in the EU. Read on to learn more about them!Medical devices include everything that goes inside the...

Articles > Business & Careers > Strategic Planning Aug 07, 2022

Author Bio

Your expert guide in the Medical Device Fraternity Maven Profcon Services Llp is a leading consultancy in the medical Device Fraternity. We provide a unique consulting experience to medical device manufacturers.