Medical Affairs

Medical Affairs

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Whilst we place great emphasis on the importance of pre and post marketing drug safety, we also place absolute value on the importance of peace of mind for both our client and our client’s stakeholders – ensuring the products are used properly and information is accurate and up to date to be provided to Healthcare Professionals and patients alike. To complement our services in clinical and post marketing drug safety, we provide interactive medical services within our Medical Affairs Group that cater to the needs of our client’s stakeholders (for medicines; devices; cosmetics; vaccines; radioisotopes) to ensure their brand is supported to the highest possible ethical standard.
PharSafer13Founded in 2003 by Dr Graeme Ladds, PharSafer® is a specialist Contract Research Organisation (CRO) in Global Clinical and Post Marketing Drug Safety, and Medical Services, with a wealth of experience in Pharmacovigilance, Auditing and Medical Affairs – and the various, numerous and extensive legal safety/medical obligations for licence holders to comply with – as well as Regulatory Strategy for the best methods for obtaining scientific advice concerning licence submissions and approvals. Together with our sister company which focuses on Training: SaPhar, PharSafer® continuously seeks new and innovative ways to provide added value for our global clients – going above and beyond expectations and optimising processes and procedures involved with clinical and post marketing drug safety and licencing approach. Our ability to offer first-class services in Pharmacovigilance, Regulatory Affairs, Training, Auditing, Medical Affairs and IT Informatics means that, for many clients, we operate as their Pharmacovigilance and Medical Departments – guiding them through the labyrinth of drug safety and medical legislation, all in the interests of ensuring patient safety and client compliance. We love what we do. We love finding solutions. Quite simply, we are by far... Your leading partner in Drug Safety.

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