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Let's Talk About
Your Trial

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.

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We respond to all enquiries within one business day.

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Contact Information

Location

Johannesburg, Gauteng
South Africa

Response Time

We respond to all enquiries within one business day (Monday – Friday, 08:00–17:00 SAST).

GCP Training Enquiries

For GCP training bookings, please indicate the number of participants, preferred date range, and delivery format (in-person or virtual) in your message.

SAHPRA Submissions

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.

Not Sure Where to Start?

Regulatory & Ethics

SAHPRA CTAs, IRB and IEC ethics submissions, protocol development and regulatory strategy.

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CRA & Monitoring

Site qualification, initiation, routine monitoring visits, SDR and risk-based monitoring.

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GCP Training

ICH E6(R2) aligned GCP training for investigators, coordinators and site teams.

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