We, Symbiorph Clinical Trialogy provide sponsor a comprehensive project plan which helps to ensures that all project requirements are met on time and within budget, so the patient recruitment will complete within the time frame. Our clinical project managers were carefully selected for their therapeutic expertise which helps in maximize flexibility, create an efficient and cost-effective monitoring process. We offer the following Clinical Project Management services:
Pre-Study Activities:
- Strategic Site Selection Process,
- Feasibility Analysis,
- Budget Negotiation,
- Arranging Investigator Meeting,
- Clinical Trial Agreement with the investigator,
- IRB & EC submission and approval process,
- Central Lab selection
- Site specific SOP development and many more …
Site Management:
- Site Initiation,
- Interim Monitoring Services,
- Informed Consent Admin Assistance,
- Protocol Specific Training,
- Patient Enrollment and management,
- IP Accountability,
- Patient Safety & compensation resolution,
- Adverse Event notification,
- Vendor Management,
- Core Lab Services Coordination,
- Sample Shipment & Central Lab Support and many more...
Post Study:
- Study closeout (LPLV),
- Data Lock time,
- Query resolution and many more...
