ACE Research is a Clinical Research Organization (CRO) providing services to pharmaceutical, biotechnology, and medical device companies helping them conduct clinical trials efficiently and effectively.

We offer a wide range of CRO services, including clinical trial management, site selection, patient recruitment, data management, regulatory compliance, quality assurance, monitoring, and more.

Companies use ACE CRO services to leverage our expertise and resources in clinical trial management. We accelerate trial timelines, reduce costs, and provide access to a global network of clinical trial sites, making the drug development process more efficient.

Choosing the right CRO depends on your specific needs. Consider factors such as the CRO’s experience in your therapeutic area, geographic reach, quality track record, and cost-effectiveness. Conduct thorough due diligence and ask for references.

ACE is involved in all phases of clinical trials, from phase I research to post-marketing studies. We provide support at any stage of drug development, depending on the client’s requirements.

We have US and Africa presence and can navigate the complexities of international trials. We ensure compliance with local regulations, language barriers, and cultural differences while maintaining consistency in trial management.

Yes, ACE play a significant role in vaccine development, including clinical trial design, site selection, patient recruitment, data management, and regulatory compliance for vaccine trials.


Scientific and Medical Expertise in Key Therapeutic Areas