OUR SERVICES
We will partner clients from the conception of their projects and provide information that will aid decisions through market study and clinical research. Services include Product Registration and Regulatory support, including Pharmacovigilance through the entire life cycle of the product.
Note; Retain the Mission and the Vision
We help our clients seamlessly enter the Nigerian market by advising on the documentation required to get regulatory approvals. Dossier compilation, document filing and follow through with the regulatory agency to ensure product registration and market entry. We are also able to act as Regulatory agents and Marketing Authorization Holder for companies requiring such service throughout the entire life cycle of the product.
We are one of the leading clinical research organizations in Africa, with operating offices in Nigeria and Kenya, will project-manage phase III and IV Clinical Trials and Bridging Studies to support Marketing Authorization Applications and achieve desired outcomes for clients. Savante is foremost among CROs in Nigeria and able to speedily get approvals for clinical trials from National Regulatory Agencies and Hospitals’ Ethics Committees. Savante Consulting Limited can help clients select Clinical Trial Sites, choose investigators, recruit patients and provide logistics for data and clinical trial materials.
We are able to serve as local Pharmacovigilance Agent for products in Nigeria. We will generate necessary documentation, to support management of ICSRs and PSURs to support continuing registration of the product in the local market. Savante will also provide training, a call desk and data management support system that meets the requirements of Pharmacovigilance guidelines of the regulatory authorities.