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TCRS is able to provide a comprehensivemed-in-petris range of Pharmacovigilance (PV) services fully customised to client requirements, working with you to meet your safety reporting and PV obligations. With our partners at Boyd Consultants, TCRS is able to provide a comprehensive range of Pharmacovigilance (PV) services fully customised to client requirements, working with you to […]
Our data management service is centred on the principle of delivering to the highest standards of quality in a timely manner. Working in close partnership with our sponsors we develop innovative statistical designs and analytical methods across a wide range of therapeutic areas. Experience includes – Bioequivalence assessment, Dose proportionality, Standard non-compartmental modelling for pharmacokinetics, […]
Our clinical monitoring service is conducted by an exceptionally experienced team. Our clinical monitoring service is conducted by an exceptionally experienced team – all our CRAs have worked in Clinical Research for at least 7 years. Because our Senior Managers have worked in hospitals and academia, they are able to build strong and effective working […]
On April 1st 2016, the new Health Research Authority (HRA) clinical research governance system was fully implemented in the UK. All UK clinical studies must follow the Health Research Authority (HRA) clinical research governance system. The founders of TCRS played a key role in developing the HRA system making us uniquely qualified to expertly navigate […]
Selecting the very best investigative sites is key to achieving your project goals. Our experience of the UK healthcare sector gives TCRS a clear advantage because we know in advance which hospitals have the expertise and infrastructure to fulfil your requirements. Our relationships with tried and tested investigators across Europe, the USA, and Australia have […]