Medical Information

By |2019-05-29T10:26:35+00:00May 29th, 2019|

Medical Information All holders of Marketing Authorisations in the European Union are obliged to maintain a Scientific Service to answer and collate medical and scientific enquiries from healthcare professionals. Our experienced team can provide a dedicated, English-language scientific service for the supply and collation of medical information, with periodic trend analysis, [...]


By |2019-05-29T10:23:04+00:00May 29th, 2019|

Development Strategic analysis and decision-making to support you through all stages of the pharmaceutical development process. We will designate a skilled and experienced project manager to act on your behalf and then create a strategy specifically designed to meet the individual needs of your project. We work with, and coordinate, [...]


By |2019-05-29T10:07:21+00:00May 29th, 2019|

Pharmacovigilance Did you know that as soon as you apply for a Marketing Authorisation, you should be conducting pharmacovigilance activities? For both medicinal products and medical devices, we can provide a full pharmacovigilance service designed to meet the complex and changing needs of the global  environment, under the direction of a [...]


By |2019-05-29T09:52:06+00:00May 29th, 2019|

Quality A sound quality system enhances organisation through an iterative process of continuous improvement. We provide European Union batch release and certification by a Qualified Person, in addition to importation and retesting. We also provide Responsible Person services to support your supply chain. We conduct GMP, GCP, GVP and GLP [...]

Regulatory Affairs

By |2019-05-29T09:51:35+00:00May 29th, 2019|

Regulatory Affairs Let our experts guide your regulatory affairs strategy to help you get the most from your products in the best possible timeframe. After the expenditure and effort of product development, it is essential to ensure that you get the best out of your investment. The field of regulatory affairs [...]