At Viopharm, we believe that successful licence approval begins with a thorough review of existing company systems; this includes quality, safety and product information.To find out more, browse through our Review Services section.

We provide support and expertise in authoring a complete dossier for your marketing authorisation application and provide full support in devising a successful submission strategy that can cover all EU markets as well as international.To find out more, browse through our Submission Services section.

We provide QC testing services, batch release and certification of your product to allow release and distribution into target markets.
To find out more browse our Supply-chain Services section

After successful marketing authorisation approval, Viopharm offers a range of post licensing services including full life cycle management, marketing support and advice to our clients to help in the establishment of a European Office. To find out more please browse our Post-licensing Services section.