Our Services
Sponsor/CRO
Feasibility
Clinical trial feasibility is a process of evaluating the possibility of conducting a particular clinical program / trial in a particular geographical region with the overall objective of optimum project completion in terms of timelines, targets and cost.
Q-max helps to evaluate data on basis of Clinical aspects, site demographics, recruitment and retention, ethical aspects, site infrastructure and quality.
![feasibility 123-01](http://q-max.in/wp-content/uploads/2022/04/feasibility-123-01.jpg)
Site Selection & Onsite Trial Management
Helps to select site on basis of Education, training, experience, Previous work in similar trials, Investigator’s site team and infrastructure, Any other protocol-specific requirements, imperative for the trial
![site selection 2-01](http://q-max.in/wp-content/uploads/2022/04/site-selection-2-01.jpg)
Project Management and Monitoring for Phase Clinical Trials
Experienced CRCs, good documentation practice, timely internal monitoring, documents verification
![project management-01](http://q-max.in/wp-content/uploads/2022/04/project-management-01.jpg)
Patient Recruitment & Retention Strategies-
Helps to recruit high numbers of patients and have innovative ideas to increase patient pool.
![Patient recruitment-01](http://q-max.in/wp-content/uploads/2022/04/Patient-recruitment-01.jpg)
Regulatory Support
Active support In regulatory audits and inspection
![Regulatory Support2-01](http://q-max.in/wp-content/uploads/2022/04/Regulatory-Support2-01.jpg)
Clinical Trial Staff Support
Providing experienced team, providing trainings to freshers and timely arrangements of GCP trainings & case study oriented training for site staffs on a regular basis.
![Clinical Trial 2-01](http://q-max.in/wp-content/uploads/2022/04/Clinical-Trial-2-01.jpg)
Investigators/Sites
![Site Close out 12-01](http://q-max.in/wp-content/uploads/2022/04/Site-Close-out-12-01.jpg)
Site Close Out
- Final study close out
- Archival of study documents
![initiation icon 12-01](http://q-max.in/wp-content/uploads/2022/04/initiation-icon-12-01.jpg)
Site Initiation
- Site Qualification Visit (SQV)
- Site Initiation Visit (SIV)
![Site Monitoring 12-01](http://q-max.in/wp-content/uploads/2022/04/Site-Monitoring-12-01.jpg)
Site Monitoring
- Query resolution
- EDC management in timely manner
![Pre-clinical trial 12-01](http://q-max.in/wp-content/uploads/2022/04/Pre-clinical-trial-12-01.jpg)
Pre-Clinical Trial Site Preparation
- Feasibility
- Site selection
- On site trial management
![data management icon-01](http://q-max.in/wp-content/uploads/2022/04/data-management-icon-01.jpg)
Data Management
- Quality Documentation and updation on time basis
- EDC completion and query resolution in timely manner
![Regulatory Support2-01](http://q-max.in/wp-content/uploads/2022/04/Regulatory-Support2-01.jpg)
Regulatory Support
- Actively supports in regulatory audits and inspections, handling and immediate query response.
Contact our team
![](http://q-max.in/wp-content/uploads/2022/03/Arif-bhai.jpeg)
Mr. Arif Mansuri
“There are always combine efforts of participants, Investigators and healthcare workers to bring new therapies. These have helped millions of people to live longer and healthier life. Q-Max Clinical Research (We) are the strongest bridge between Investigators, Participants and CRO/Sponsors.”