Medical Device manufacturers must use the appropriate documentation that adheres to the standards provided by the Food and Drug Administration’s (FDA) guidelines. Intellect offers a highly flexible software solution for the automation of the design process for all medical device manufacturers.
Intellect can help standardize and automate processes for drug safety reporting to meet compliance and to improve operational efficiency with a highly flexible workflow automation solution.
With Intellect, organizations can manage and track all communications concerning product registrations, submissions, and commitments to health authorities.
Give Intellect a try today and see what it can do for your business.