We follow our own ICH and EU Directive compatible SOPs, bi-annually updated, but we are able to operate also under client’s SOPs. A Quality Management Handbook has been developed in collaboration with our AcrossAlliance partners.
Project oriented approach involves careful planning, risk assessment and tracking all key parameters of the study, allowing an early detection of problems and effective application of corrective actions. Pharmnet CRAs focus on detailed evaluation of source documents on site, which minimizes the probability of non-reporting critical events.
Our staff participate in a continual training within and outside the company.
Pharmnet training methods passing the “company memory” to all employees
qualify the CRAs for providing advice and support to investigators in unexpected
and atypical situations. Scientific methodology training qualifies the CRAs for
making decisions with a full awareness of their reason and ultimate impact on
the study.