Imposant Research & Consultancy Pvt Ltd.
Driving Smarter, Faster, Ethical Clinical Research
Why Choose Imposant Research & Consultancy ?
We identify and evaluate potential investigator sites based on therapeutic expertise, infrastructure, and patient pool to ensure smooth study start-up and realistic feasibility outcomes.
Regulatory & Ethics Committee Coordination
Our team provides comprehensive assistance in preparing and submitting regulatory and ethics committee documentation, ensuring compliance with ICMR, GCP, and Schedule Y requirements.
Site Initiation and Training
We coordinate site initiation visits, investigator meetings, and protocol-specific training sessions to ensure all site staff are adequately prepared for study conduct.
Clinical Trial Coordination
Trained clinical research coordinators handle day-to-day study activities, including patient screening, informed consent, visit tracking, data documentation, and monitoring support.
Patient Recruitment and Retention
We leverage a patient-centric approach and local outreach strategies to achieve timely recruitment while maintaining high ethical standards and patient satisfaction.
Quality and Compliance
Regular internal audits and SOP-driven practices ensure sites remain inspection-ready and compliant with international and national guidelines.
IP & Study Material Management
We assist in investigational product receipt, storage, accountability, temperature monitoring, and reconciliation to maintain full traceability.
