Our Mission and our value:
ACTG-CRO is a privately held company composed of 3 departments:
CRO services Department (Sites & Investigators Selection, Clinical Trials Monitoring, Remote Centralized Monitoring, SMO, Outsourcing Staff, Bioequivalence Studies (BE Center is WHO certified), Biostatistics...)
Pharmaceutical Marketing Department (Business Expansion Strategies for Pharmaceutical Companies which would like to expand their Business in Africa and Middle-Eastern Countries: Registration, Market Studies, Medical Promotion, Distribution...)
Training Department (CRAs, Medical Representative, Product Manager...)
Our company is a go to partner for many sponsors seeking to conduct clinical trials in Africa. We bring a tremendous amount of localized knowledge and site management services and we collaborate with research organizations and biopharma sponsors to make clinical trials available in Africa. We are in touch and cooperating with numerous hospitals and investigation sites in Africa and we have actually 20 Sites Partners in Africa with their number of potential recruitment for each therapeutic area in each site.
To improve health and to improve life in African countries, by improving access to healthcare through clinical studies. We deliver what we promise with honesty and integrity, thus earning the trust that fosters long term relationships.
To provide professional, cost-effective and timely assistance to our Clients to contribute to their drug development efforts and to guarantee the collection of high-quality clinical data in Africa in compliance with international standards and local regulations that warrant subject protection.
To become the leading experts in clinical trials in Africa and Business Expansion for Pharmaceutical Companies due to our quality services, the guarantee of study subject protection and establishing long-term trusting relationships with our Partners and Clients.
ACTG-CRO (Africa Clinical Trials Group) is a regional Full-Service CRO (Contract Research Organization) and a Vendor for pharmaceutical, biotech companies and CROs globally providing Clinical Operations services (Medical Writing, Clinical Monitoring, Business Expansion, PV, etc.), preparing FDA/EMA submission-ready packages and local african countries regulatory submissions, to conduct their clinical trials in Africa. ACTG-CRO is committed to implementing International Standards in Clinical Trials. ACTG-CRO is headquartered in Tunisia and operates in most African countries.
ACTG-CRO being a multicultural company, the team, experienced in working in international companies, is able to communicate efficiently with international Clients. ACTG-CRO's employees have a great experience and great understanding of the importance of time in clinical trial to market. Our ability to deliver High Quality results is based on recruiting and maintaining the best talent within our Organization.
ACTG-CRO has formed strategic development partnerships in Africa with a list of investigators experienced in clinical trials. One of our goals is to improve access to healthcare for patients in Africa by assisting local investigators, with our SOPs established according to FDA recommendations, to the smooth conduct of your clinical trials.
Patients recruited in the clinical trials will have access to healthcare, diagnosis and treatment which could benefit them and contribute to Clinical Research.
With our local presence in African countries, clients are guaranteed that their trials will be conducted according to international standards. We assign locally-based CRAs trained to clinical trials regulations and SOPs (both company and sponsor SOPs).
The fact we run operations from Tunisia, apart from Europe, US enables us to provide very competitive rates.
We provide you Clinical Sites to implement your trial.
With our Expertise in clinical trials and our list of Experienced Investigators specialized in a range of therapeutic areas with whom we entertain great relationships, we are ensuring to provide the services you need with the excellent process.
We have great relations with Regulatory Authorities, Ethics Committees and we know the local process for documents submission.
We are in close contact and cooperating with the Ministry of Health of Tunisia.
We have comprehensive and detailed SOPs to guide and train all the staff, to ensure operations to be carried out in compliance with ICH/GCP Regulations and to fulfill Sponsor requests and requirements.