Services
| Service | Description | Timeline | Price |
|---|---|---|---|
| Orphan Drug Designation | Prepare and submit applications for orphan drug designation to regulatory agencies. | 8-12 weeks | $20,000 - $40,000 |
| Regulatory Submissions | Prepare and submit documentation to regulatory agencies for product approval. | 8-12 weeks | $40,000 - $80,000 |
| Regulatory Document Submission | Prepare and submit regulatory documents to agencies like the FDA and EMA. | 6-8 weeks | $15,000 - $30,000 |
| Pricing and Reimbursement Analysis | Analyze pricing strategies and reimbursement pathways for drug products. | 4-6 weeks | $15,000 - $30,000 |
| Patient-Reported Outcomes | Develop and validate patient-reported outcome measures for use in clinical trials. | 8-12 weeks | $20,000 - $40,000 |
| Clinical Data Management | Manage and process data from clinical trials to ensure accuracy and integrity. | 8-10 weeks | $25,000 - $50,000 |