Pharmacovigilance

We place the highest importance on patient safety. Our Pharmacovigilance (PV) infrastructure reflects this, ensuring that we remain compliant with reporting requirements and flexible to future needs and trends.

Our PV team has been structured to provide processes and infrastructure that can fulfill the requirements of a modern pharmacovigilance system. It is an agile system, designed to support today’s needs and be flexible enough to adapt to tomorrow’s requirements.

To report an Adverse Event, please contact:

Pharmacovigilance

Medical Information

Our Medical department predominantly focuses on Medical Information, but also has input into marketing activities, product quality and customer liaison.

Our professionals are on-hand to answer any questions on our products.

Contact a Medical Information Professional

Medical Information

Regulatory Affairs

Our Regulatory Affairs department is responsible for a wide range of activities which include the licensing process for new products and variations to existing licenses.

Regulatory Affairs work also involves the maintenance of Summary of Product Characteristics (SPC) and Patient Information Leaflet (PIL) publishing, as well as managing partnerships and distributor markets.

Regulatory Affairs