Questra provides classic CRO services in clinical trial management. In addition, we offer clinical trials operational support, data management, analytical and document writing that meets your clinical trial needs. Our skilled personnel are familiar with available research infrastructure in the northern region, are equipped with local knowledge and have the agility to develop customised offerings i
n key therapeutic areas that are best suited for our multi-ethnic patient population. We assure you with high quality data that meets your timelines, complies with safely standards and is cost effective. Questra offers comprehensive clinical trial management services that meet your specific needs:
Protocol Design and Development
> Feasibility Studies
> Site & Investigator Identification
> Contract and Budget
> Study Initiation
> IRB and Regulatory Affairs
> Clinical Trial Project Management
> Clinical Trial Monitoring
> Clinical Trial Logistics
> Safety Surveillance
> Archiving
> Medical Writing
> Training and Consultation in Clinical Research
> Training and Consultation in Bioavailability and Bioequivalence studies
> Clinical Pharmacokinetics & Pharmacodynamics Studies
> Laboratory Services
> Data Management & Bio-statistical Analysis
