Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Process Development | Optimize the manufacturing process for drug products. | 12-16 weeks | $50,000 - $100,000 |
| Regulatory Submissions | Prepare and submit documentation to regulatory agencies for product approval. | 8-12 weeks | $40,000 - $80,000 |
| Site Selection and Feasibility | Identify and evaluate potential sites for clinical trials. | 6-8 weeks | $10,000 - $20,000 |
| Analytical Testing | Conduct laboratory tests to ensure the quality and safety of drug products. | 4-8 weeks | $15,000 - $30,000 |
| GMP Audits | Conduct audits of manufacturing facilities to ensure compliance with GMP standards. | 2-4 weeks | $10,000 - $20,000 |
| Scientific Advisory Board Management | Organize and manage meetings with scientific advisory boards to guide research and development. | Ongoing | $15,000 - $30,000 annually |