Phase I-III Clinical Trials

ACE Research is a full service CRO and has comprehensively planned and managed Phase I-III clinical trials. We have managed projects in most countries in Africa. Our company is founded and led by clinical research professionals who are passionate about their work. ACE Research is a combination of outstanding professionals, detailed processes, and rigorous quality and oversight practices.

Expert Program Management

ACE Research's Program and Project Managers are both subject matter experts as well as skilled Project Managers. They understand the details of clinical trials as well as the techniques to manage timing, cost, and deliverable quality. With the ability to assess plans and anticipate both scientific, logistical, and compliance issues, ACE Research has an outstanding track record for delivering on time, cost, and with accurate and quality deliverables. Our Project Managers' backgrounds include:

Clinical trials and regulatory experience.

Science backgrounds that allow managers to proactively address trial details and potential issues. They are well versed in Human Subjects Protection (HSP) and can plan to meet all the associated requirements as well as assures the safety of enrolled patients. A can-do, team player approach to clinical trials, meaning they pitch in where needed and are an integral part of their project teams.

Clinical Trial Efficiency

ACE Research’s Program and Project Managers are well versed at the logistics aspect of trials. Our Program Managers are supported by a detailed library of process and procedures that they use to manage every aspect of a trial. ACE Research has partnerships with leading academic institutions and international clinical trials partners that allow our Project Managers to structure each trial to the best advantage.

Accurate Data

ACE Research has a full Data Management team to assure that your primary asset - your data - is accurate and auditable. ACE Research uses Oracle Clinical™ for its Clinical Data Management (CDMS) system and can provide trials with remote data capture (RDC) or paper input to optimize any situation. The team will work closely with the staff creating the protocol and develop the CRFs, as well as build and certify the database. Our reputation for both efficiency and accuracy is unsurpassed and makes our data management a real strength of the overall ACE Research clinical trial offering.

Oversight and Quality

ACE Research has a long history of monitoring. It is viewed as the linchpin of the trial. ACE Research has a pool of veteran monitors that cover domestic and international locations, as well as a proven library of SOPs and work instructions. ACE Research has built a Virtual Office specifically to support the geographic diversity inherent in monitoring in Africa. The Virtual Office enables monitors to stay connected and is supported by a web-based backbone that provides access to SOPs, work instructions, forms, and project details. ACE Research also has in-country personnel in popular trial locations such as Kenya, Tanzania, Uganda, South Africa, Ghana, Sierra Leone, Liberia, Guinea and Gabon

Want to accelerate clinical trials in Africa? 

Contact us for Updated Regulatory Guidelines, High Enrolling Sites & Investigators, Clinical Monitoring  & much more.
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