Klintelligen being pioneer in Site Management Organization provides quality service to CROs and other medical sectors for conducting clinical research studies from beginning to the end. As a Site Management Organization we coordinate with you to organize, conduct and complete successful Clinical trials.
Klintelligen works towards fast turnaround time and thus cut down the probability of delayed schedules. We serve all therapeutic segments and renders support to CROs and medical sponsors for the investigations without delay. The rationalized process is been followed to bring effective site management services.
Investigator & Site interest
Patient population to determine capacity and speed of enrolment
Possible confounding factors in patient recruitment
Availability of referral networks
Track Investigator experience
Successful patient recruitment
Assessment of enrolment and retention in similar studies
Availability of qualified site personnel
Monitors the availability of facilities required for trials
Impact of study procedures on Standard of Care
Additional sponsor requirements
The Clinical trial management projects are administered with our standard approach. A troop of proficient members dedicatedly strives to efficiently manage the process throughout the clinical practices.
Study start-up
Investigator site selection
Project Milestones Planning
Organizing Investigator meetings
Investigator personnel training
Provide input in essential trial documents
Facilitate study activities
Monitor budgets and associated financial procedures
Management of clinical trial supplies
Monitor the study throughput the process
The clinical trials are effectively conducted, recorded and reported based on the requirements. The trials are ethnically monitored delivering accurate and legible data. We deliver the excellence with complete control over the clinical trials keeping intact of the quality.
Investigator Identification
Site Qualification Visits
Key Personal Trainer
Planning Investigator Meetings
Site Initiation Visits
Site Staff GCP and Protocol Training
Interim Monitoring Visits
Blinded and unblinded IP Accountability
Study Termination Visits
Klintelligen operates with the proficient clinical coordinators for each clinical trial. We provide excellent support system for the investigators and clinical staffs. The standard methodology is followed ensured to follow the strict guidelines. Klintelligen has highly experienced study coordinators. This unique resource helps you to overcome the many challenges of recruiting in trials.
Executing successful patient recruitment on time and on budget
Working through local ethics and regulatory approval processes
Ensuring that we meet cultural and language demands of working in diverse parts of the world
Klintelligen maintains high standard in data management system with the assured GCP. From the start to the end, every aspect of the process is streamlined and kept in track. The support system is enabled for the customer to achieve the end result.
Case Report Form and Database design
CRF review
Data validation plan (DVP)
Edit check Procedures
Data management plan (DMP) design
Quality control of database
Query management system
SAE data reconciliation
External data administration and integration
Database freezing and locking
Building and Maintenance of Clinical Trial Data Repository based on www.torqeyeanalytics.com
Healthcare analytics to excavate the accurate and required data from the widen web area. The valuable data enhances the patient care facility, monitors and maintains the patient’s database, improvise the service quality, provide transparent service and guides in decision making. Torqeyeanalytics Health Care
Therapeutic Area
Trial Site at any Global Location
Principal Investigator
Medico Legal Cases
IPR of Drug Molecule
Clinical Research Courses
An advanced clinical research training centre to lay a strong platform for the healthcare professionals, graduates for their enhancement in the respective healthcare field. Newbies lay solid foundation for their betterment in placement.
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