With a diverse economy combined with a large ratio of pharmaceutical imports, the Republic of Ghana boasts a viable future for foreign medicine and medical device manufacturers to invest in the region. Manufacturers, however, are obliged to obtain market authorizations from the Food and Drug Authority Ghana, the agency which controls registrations and licenses. The complex regulatory documentation and critical regulatory requirements might challenge foreign manufacturers to cope with Ghana market authorizations.
Pharma Wizardās panel of regulatory experts with comprehensive knowledge of Ghanaian regulatory affairs assists foreign manufacturers in navigating the regionās regulatory procedural challenges not only in a streamlined manner, but also in a compliant way. Pharma Wizardās regulatory services in Ghana span across
Medical Devices
Pharmaceuticals / Drugs
Ayurvedic Products
Pharma Wizard Offerings
Strategic Regulatory Consulting
Regulatory Roadmap for Market Access
Regulatory Affairs & Regulatory Intelligence
Registration Pathways and License Management Services
Market Authorizations
Regulatory Submissions
Submission of Site Master File (SMF), INDs
Dossier Preparation
Compilation and review of package inserts, patient information leaflets, and labels
Package Insert (PIL)
Pharma Wizard Advantages
Strategic and well-versed local regulatory knowledgebase ā with Ghana Standards Authority, Pharmacy Council, Environmental Protection Authority, and Ministry of Health / Ghana Health Services
Expert Regulatory team with proven global RA expertise
Proactive and Collaborative approach
Quick turnarounds and faster time-to-market
Keeping abreast with region-specific legislation and Regulatory guidelines