Pharmaceutical, biotechnology and laboratory industries are challenges with some of the most complex and scrutinized regulations, while also facing competitive pressures to succeed in the global marketplace.
Intellect can help enable your organization to effectively comply with 21 CFR Part 11, GxP, and other industry standards and regulations. Intellect offers a comprehensive and highly configurable QMS solution for pharmaceutical, biotechnology and laboratory organizations.
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.