- Our skilled team of pharmacists and medical doctors has many years of experience in the development of generic products within the European Union. We recognize that no two development projects are the same and that each customer has its own goals. That's why we tailor our services not only to meet or exceed EU regulatory agencies needs but to meet specific customer's requirements.
- Our knowledge in regulatory affairs assures that the achievements and results from the development work are presented in an agency friendly way, to ensure fast and successful registration.
- Together with our partner companies we offer the development of solid and liquid dosage forms, effervescent tablets and injectable forms.