Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Supply Chain Management | Manage the logistics and supply chain for clinical trials and manufacturing. | Ongoing | $30,000 - $50,000 annually |
| Process Development | Optimize the manufacturing process for drug products. | 12-16 weeks | $50,000 - $100,000 |
| Regulatory Strategy Consulting | Provide advice on regulatory strategy for product development and approval. | 4-8 weeks | $15,000 - $30,000 |
| Scientific Advisory Board Management | Organize and manage meetings with scientific advisory boards to guide research and development. | Ongoing | $15,000 - $30,000 annually |
| GMP Audits | Conduct audits of manufacturing facilities to ensure compliance with GMP standards. | 2-4 weeks | $10,000 - $20,000 |
| Health Technology Assessment Submission (HTA Submission) | Analyze and submit the considerations of a drug, device, or clinical procedure to regulatory agencies. | 10-14 weeks | $35,000 - $70,000 |
| Clinical Trial Design | Develop study-related protocols, case report forms (CRFs), and database tools. | 8-12 weeks | $20,000 - $40,000 |