Evnia proudly announces the successful completion of another ISO 9001:2015 audit for our well-established consulting services for our Clinical and Regulatory Affairs Departments and our Authorized Representative operational branch.
Months of hard teamwork, commitment to excellence, and intensive preparation led to a zero-findings result AGAIN!
Having earned a stellar reputation for providing realistic, workable solutions to our partners’ regulatory challenges, Evnia will continue to consistently develop high-quality regulatory strategies and monitor their implementation, thus supporting MedTech, Biotech, and Pharma stakeholders to the desired outcome.
Why Evnia?
Because you are looking
- for access to in-house, cross-functional, field-experienced regulatory professionals from various fields
- to reduce the risk of non-compliance
- to shorten your time to the market
- for practical solutions that will prevent unnecessary costs and delays
Contact us today for an introductory discussion!
