Primorus founders provide diverse experience including; managing NZ Regulatory submissions for blue chip pharma for many years, previous membership on NZ regional Ethics Committees, managing one of the largest clinical trials centres in Europe, project managing clinical pharmacology studies for blue chip Pharma, managing studies at the MRC (Medical Research Council, UK), managing an NZ based CRO. Our principal investigator has a specialist qualification in conducting clinical trials from the Royal College of Physicians, UK. This is recommended as the primary qualification for conducting phase I trials by the ABPI (Association of the British Pharmacuetical Industry).

In addition to conducting early phase trials we partner with external Therapeutic Area Specialists in the conduct of phase II trials to provide dedicated and experienced staff, facilities, standardised procedures and an on site Principal Investigator.

We partner with academic units to conduct academic studies, in line with our strategic goals of furthering research in New Zealand.

Our end to end early phase sevice includes:
Regulatory, Ethics and Local Sponsorship
Recruitment Specialists
Inpatient and Outpatient State of the Art Facilities incorporating internal SOPs and e-Learning staff development programs
EDC, Data Management and Biostatistics
Medical Writing including Protocol Development, Report Writing and Medical Monitoring
Training