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Clinical Operation

G7 Synergon's Clinical Operations team conducts Phases II-IV clinical trials by maintaining the highest standards of ethics, quality and confidentiality. We promote a team approach with emphasis on

 management, support, recognition, training, accountability and personal development. To ensure that our clients receive quality monitoring services in compliance with the applicable regulatory guidelines, we provide comprehensive training and development programs to our Clinical Research Associates (CRAs).

Feasibility And Planning – Key To A Successful Completion Of The Study

Feasibility looks into the disease prevalence, incidence rates and current pattern of enrolment in similar trials or therapeutic areas. Besides considering medical, statistical, ethical and regulatory requirements, comprehensive feasibility reports help to make critical decisions of the planned study. Trial specific risk assessment and quality planning are an integral part of our trial preparation procedures.

Project Management

Team Approach – We Streamline Our Team According To The Client's Needs

G7 Synergon understands that project management is an integral part towards the success of a clinical trial. The project management team is responsible for ensuring that studies are kept on track as per the regulatory norms. Outsourcing your project management needs to G7 Synergon simply means, your project would be managed by a highly dedicated interdisciplinary team, steered by a project expert, who is the key point of contact with the client for any issues throughout the project. We have an outstanding track record of continuity in our project management teams, which in turn significantly facilitates communication with the client’s study team. Project teams are trained in advance for each study with regard to the study's medical background, study goals and study plan.

Our Project Management services include:

• Project Management Planning
• Feasibility and Patient Access Planning
• Subject Recruitment & Retention Strategies
• Collecting and Reviewing Initial Essential Documents
• Ethics committee Submission /Approvals
• Therapeutic and project specific training
• Clinical Trial Agreement preparation
• Detailed risk assessment including risk management plans
• Project budget controlling



Medical Monitoring

All trials are monitored in accordance with G7 Synergon’s Standard Operating Procedures (SOPs) developed to meet Good Clinical Practice (GCP) standards. Our CRAs have considerable clinical research expertise and broad therapeutic experience on the Paper – based and Electronic Data Capture (EDC) platforms. We have co-monitoring and training programs to ensure ongoing quality, consistency and up-to-date knowledge in our monitoring.

At G7 Synergon, we believe that monitoring is not only about making sure that the project runs smoothly with minimum protocol violations and low query rates, but also about delivering personalized services. Our CRAs produce a dynamic, rewarding and mutually beneficial site and client relationship.

Medical Monitoring Services

• Assessing sites for feasibility to conduct study
• Investigator site selection and Set Up
• Pre-study Qualification visits
• Initiation of the sites on completion of start up activities
• Periodic Monitoring visits
• Source Data Verification
• Query Resolutions
• Adverse Event management
• Study Close out Visit




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