Management and Preparation of Pre & Post Marketing Registration Submission Applications & Maintenance Projects

Do you need assistance with all you regulatory documentation needs such as preparation of Investigational Medicinal Product Dossiers (IMPDs) or clinical trial applications (CTAs),marketing authorisation applications (MAAs), variations, paediatric Implementation plans (PIPs), scientific advice briefing dossiers etc? CAMPHARM has many years experience and good relationship with the regulatory agencies in the EU.

Need regulatory assistance with all your regulatory submission needs?

Perhaps CAMPHARM can help – contact us?