Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Pharmacovigilance Services | Monitor and report adverse effects related to drug use. | Ongoing | $20,000 - $40,000 annually |
| Clinical Trial Monitoring | Oversee the conduct of clinical trials to ensure compliance with protocols. | Ongoing | $10,000 - $20,000 per site |
| Real-World Evidence Generation | Collect and analyze real-world data to support regulatory submissions and market access. | 12-24 weeks | $30,000 - $60,000 |
| 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 |
| Consensus Reports | Develop and submit a report that examines a scientific or medical issue. | 4-6 weeks | $5,000 - $10,000 |
| Stability Studies | Evaluate the stability of drug products over time. | 12-24 months | $50,000 - $100,000 |
| GMP Audits | Conduct audits of manufacturing facilities to ensure compliance with GMP standards. | 2-4 weeks | $10,000 - $20,000 |