REGULATORY AFFAIRS
Vifor Pharma can provide support in the preparation and submission of product registration files. Specific expertise includes:
_development of a complete CTD technical documentation (modules 2.3 and 3)
_expertise in regulatory requirements for
_development of a complete CTD technical documentation (modules 2.3 and 3)
_expertise in regulatory requirements for
- drugs (EU)
- medical devices
- nutraceuticals
- cosmetics
_support for submission and notification to the relevant authorities.

