We offer comprehensive regulatory support for human medicinal products, veterinary medicinal products and herbal medicinal products in Europe. From dossier compilation to registration and later life cycle management activities, our business-minded team ensures high quality work, but also keeps an eye on the implications for costs and time.
Our objective: The fastest approval at minimal costs.
Our team of highly qualified up-to-date regulatory affairs personnel includes pharmacists, biologists and chemists.
We have expertise covering a variety of therapeutic areas such as CNS, eye care, oncology, urology, gynaecology, gastro-enterology, cardiology, including different pharmaceutical forms such as oral, parenteral and sterile topical formulations.
We regularly assist small, mid and big pharma customers with our regulatory affairs services.