Accacia Serum provides management of clinical trials in phase II and III of IVD and pharmaceutical products. Its clinical, scientific, regulatory and professional staff delivers full range of services from protocol design to post-market surveillance. Accacia Serum, with its network of global principal investigators and clinical resources, is able to bring the product to the market faster. . We provide a unique brand of experience, personalized research services and flexibility, which keep our clients coming back.

·     Accacia Serum’s Clinical Research Services specializes in project management, clinical monitoring, data management, quality assurance, and regulatory affairs for our clients.

·     Our global team of principal investigators has access to the most significant and rare global patient populations for your clinical research needs. The Clinical Research Services staff has successfully completed clinical studies in N. America, Africa and Asia. 

·     We have dedicated IRB/IEC/MOH liaisons that work side-by-side with study coordinators to expedite the approval process. 

·     Accacia Serum’s Bio-repository services enable us to have short or long-term storage of samples. 

·     In-house analysis of samples collected at our trial sites. 

·     Consulting services to prepare submissions to relevant regulatory bodies, such as the US Food & Drug Administration (FDA). 

·     Accacia Serum can provide clients with confidential online access to study data — monitoring critical document collection, patient enrollment and visit activity, screen failures, early withdrawals, case report forms, and investigator payment activity.

·     Use of global clinical resources and efficient management will help you bring your product to market faster.