Product Registration
End-to-end regulatory affairs services
With our technical registration expertise and in-depth regulatory knowledge, we are well-positioned to ensure the successful registration of your products:
STEP
01
Pre-registration
- Regulatory feasibility assessment
- Evaluation of product risk classification, registration and licensing requirements
- Gap analysis
STEP
02
Registration
- Review and prepare application dossier
- Submission to regulatory agencies
- Registration follow-up and monitoring
STEP
02
STEP
03
Post-Approval
- Review of marketing and advertising materials
- Managing product variations or re-classifications
- Renewal of product registration or licence
- Pharmacovigilance reporting