Whether you need regulatory support, site monitoring, GCP training or are simply exploring options for your South African trial — we'd like to hear from you.
We respond to all enquiries within one business day.
Johannesburg, Gauteng
South Africa
We respond to all enquiries within one business day (Monday – Friday, 08:00–17:00 SAST).
For GCP training bookings, please indicate the number of participants, preferred date range, and delivery format (in-person or virtual) in your message.
For regulatory support, it helps to share your therapeutic area, trial phase, anticipated CTA submission date and any specific timelines or constraints you are working to.
SAHPRA CTAs, IRB and IEC ethics submissions, protocol development and regulatory strategy.
Learn moreSite qualification, initiation, routine monitoring visits, SDR and risk-based monitoring.
Learn moreICH E6(R2) aligned GCP training for investigators, coordinators and site teams.
Learn more