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| Stage | Description | Duration | Key Activities | Responsible Parties |
|---|---|---|---|---|
| Concept Development | Initial research and idea formulation for Retatrutide. | 2 months | Market analysis, feasibility studies. | R&D Team, Marketing Team |
| Preclinical Trials | Testing safety and effectiveness in preclinical studies. | 6 months | Animal testing, safety assessments. | Clinical Research Team, Regulatory Affairs |
| Clinical Trials Phase 1 | Testing on healthy volunteers to assess safety. | 1 year | Dosage determination, monitoring. | Clinical Operations, Ethics Committee |
| Clinical Trials Phase 2 | Testing effectiveness in patient groups. | 1 year | Efficacy studies, dosing adjustments. | Clinical Research Team, Data Analysis Team |
| Regulatory Submission | Preparing and submitting documentation for approval. | 3 months | Compilation of study results, regulatory filings. | Regulatory Affairs Team |
| Post-Marketing Surveillance | Monitoring safety and efficacy in the general population. | Ongoing | Data collection, adverse event reporting. | Pharmacovigilance Team, Marketing Team |