Pharmaceutical /Drugs Registration
We provide end-to-end support, from submitting applications to holding marketing Authorizations , ensuring a seamless approval process.
Dossier preparation and regulatory submissions
Drug classification and approval strategies
Authorized Local Representation
Pharmaceutical Product Classification
Pharma Market Access & Marketing Insights
End-to-end Pharmaceutical Product Registration
Gap Analysis, Pharmaceutical Dossier Preparation, and Submission to the National Pharmaceutical Regulatory Agency (NPRA).
Preclinical Services (Generation of Scientific Reports for Regulatory Submissions).
Import License Application.
Change of the Product Registration Holder
Ad-hoc Regulatory Affairs Consultation.