Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Real-World Evidence Generation | Collect and analyze real-world data to support regulatory submissions and market access. | 12-24 weeks | $30,000 - $60,000 |
| Clinical Data Management | Manage and process data from clinical trials to ensure accuracy and integrity. | 8-10 weeks | $25,000 - $50,000 |
| GMP Audits | Conduct audits of manufacturing facilities to ensure compliance with GMP standards. | 2-4 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 |
| Emerging Market Opportunities | Analyze risks and opportunities in new markets for patient access to new treatments. | 6-8 weeks | $15,000 - $30,000 |
| Stability Studies | Evaluate the stability of drug products over time. | 12-24 months | $50,000 - $100,000 |
| Data Visualization | Visualize data collected from clinical trials and/or clinical research. | 3-5 weeks | $3,000 - $7,000 |
| Regulatory Submissions | Prepare and submit documentation to regulatory agencies for product approval. | 8-12 weeks | $40,000 - $80,000 |