Medical Monitoring

Our Medical Monitors come from diverse therapeutic backgrounds, and have the clinical and research expertise required to provide medical oversight of clinical trials.

George Clinical’s Medical Monitoring team provides the clinical and research expertise required to deliver rigorous medical oversight for all aspects of a clinical trial.

George Clinical’s Medical Monitoring services are provided through the Medical and Safety Services Group. Our Medical Monitors come from diverse therapeutic backgrounds, and have the clinical and research expertise required to provide medical oversight of clinical trials. According to the needs of the trial, our Medical Monitors are able to provide a number of services, such as:

medical monitoring
  • Providing input into the study protocol, informed consent forms, project risk assessment
  • Training investigational sites and study teams
  • Supporting investigational sites with queries around eligibility, safety etc.
  • Reviewing SAEs, coding of SAEs and writing safety narratives
  • Reviewing patient data to identify trends and risks across the study

Our Medical Monitors are regionally located to provide complete coverage for investigational sites in various time zones. In addition, appointment of local medical monitors provides the added benefit of communication in the local language, and a familiarity with local clinical practices and culture, which in-turn, helps to foster stronger ties with investigational sites and study teams. Our Medical Monitoring Team operates in Australia, New Zealand, China, India, Taiwan, Japan, South Korea, Malaysia, Philippines and Hong Kong.

Medical Monitors provide rigorous medical oversight from design to delivery.

George Clinical – Medical Monitoring

Video Transcript

In today’s high-cost, high-risk clinical trials environment, you need medical monitoring that you can trust.

At George Clinical, our medical monitoring team will provide rigorous oversight for all aspects of your clinical trials; from design through delivery.

Plus, our medical monitors are regionally located, providing you with complete coverage for investigational sites in various time zones.

By localizing our medical monitors, you’ll get the added benefit of improved communication in local languages and dialects, as well as familiarity with local clinical practices and culture. This helps foster stronger ties with investigational sites and study teams.

George Clinical’s medical monitoring services are provided through the Medical and Regulatory Services Group. Our medical monitors come from diverse therapeutic backgrounds, and have the clinical and research expertise required to provide rigorous medical oversight of clinical trials.

Get access to a number of services, including: Input into the study protocol, informed consent forms, and project risk assessment; training investigational sites and study teams; supporting investigational sites with queries regarding eligibility, safety, and other such matters; reviewing SAE’s, coding of SAE’s, and writing safety narratives; and reviewing patient data to identify trends and risks across each study.

For clinical trial design and delivery executed to the highest clinical standards, get in touch with George Clinical today through our website: www.georgeclinical.com.

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