About Us

Integrium South Africa
Your Gateway to Clinical Trials in Africa

Integrium South Africa (SA) is a well-established Contract Research Organization providing a comprehensive range of clinical research and development services to pharmaceutical, biotechnology, and device companies.

We provide integrated and turnkey clinical trial services and strategies in support of our sponsors’ clinical development and marketing objectives. Our strong capabilities, in-depth knowledge of the local market, and experienced staff make us an ideal partner for companies sponsoring clinical trials in South Africa and the larger region.

Services

Integrium SA provides a comprehensive range of services, including:

  • Feasibility assessments
  • Site recruitment and contract negotiation
  • Project management
  • Clinical monitoring
  • Regulatory services
  • Drug safety and medical services
  • Drug management
  • Vendor management
  • Protocol development
  • Key Differentiators

What makes Integrium SA stand-out as a CRO partner for South Africa?

  • One-stop solution:
    Integrium SA offers comprehensive and integrated operational and clinical services to support and coordinate the main components of trial work scopes. Our relationship with Integrium in the USA, one of North America’s premier CROs for conducting clinical trials in cardiovascular and metabolic disease, provides Integrium SA with access to full-service multinational capabilities.
  • Speed of start-up:
    Our in-depth knowledge & experience with regulatory processes enables us to efficiently navigate the approval process and ensure prompt site activation.
  • Faster study completion:
    Our ability to recruit and motivate a network of high performing sites enables rapid enrollment and faster study completion.
  • Cost:
    Integrium SA provides competitively priced services due to our efficient infrastructure and wide network of regionally-based monitors. By in-sourcing specialized resources that already exist in South Africa, clients pay only for the CRO services they require and not for the hidden costs of a heavy infrastructure.
  • Confidence:
    Our ability to conduct thorough feasibility analysis, develop contingency plans, and maintain vigilance throughout the study enables confidence among our sponsors that we are properly prepared and are proactive when challenges arise. The team has the “local” expertise to guide sponsors through the unique clinical trial landscape and regulatory process in the country.
  • Personal Service:
    We establish and sustain a high level of attention and visibility to every workscope throughout the duration of the project and provide optimal communication due to the manageable size of organization.
  • Quality:
    We ensure high quality by selecting the best available research sites, investigators and monitoring staff, and by working in strict accordance with ICH & South African GCP Guidelines and established metrics for monitoring services.
  • Flexibility:
    We have the ability to take on global “megatrials,” but remain flexible enough to provide an individual, highly personalized service for locally managed projects. We adapt our approach as customer requirements change.