Clinical Research Services

Clinical Research Services

Our expert teams work closely with sponsors to tailor the best solution for each project and to deliver clinical trials to the highest quality. Reduce your R&D costs by outsourcing all your clinical research services under one provider. George Clinical offers a full range of clinical trial implementation services across the Asia-Pacific region and the […]

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November 15th, 2019

Real World Evidence (RWE) Research and Observational Trials

George Clinical are experts at helping sponsors balance the complex demands associated with real-world “evidence” or late-phase trials – protecting patient safety, designing clinically relevant studies, implementing simplified study techniques, building exposure to best practice and producing evidence to maximize commercial opportunities. George Clinical’s vast experience implementing these studies and its enviable global investigator networks […]

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October 26th, 2018

Regulatory Services

The George Clinical regulatory team assists sponsors through the various regulatory and institutional review boards and ethics committee processes to ensure the most efficient start-up of a clinical trial. George Clinical are regional experts in unlocking the pharmaceutical and medical device regulatory landscape of the Asia-Pacific: Australia, China, India, Japan, South Korea, Hong Kong, Singapore, […]

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July 29th, 2018

Medical Writing

George Clinical provides analysis and medical writing services for both investigator initiated and industry sponsored trials. We have the capabilities to provide the following medical writing services: Protocol Development George Clinical provides sponsors with extensive experience in the development of protocol for every phase in a global working environment. We know first-hand how patient care […]

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June 29th, 2018

Health Economics

George Clinical’s Health Economics team provide an expert, customized service to medical device and pharmaceutical companies who are increasingly expected to provide comprehensive evidence regarding the economic benefit of their product, effectiveness and necessary health impact costs. As the levels of chronic illness increase globally and the technologies available for treatment become increasingly expensive, significant […]

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June 29th, 2018

Statistics Services

The George Clinical statistics department operates globally to provide data and expertise that will enable faster, more informed decisions with reliable and flexible service. The biostatistics team has extensive experience in the design and analysis of clinical trials in a wide range of therapeutic areas. Solutions are tailored to customers’ requirements include Phase I – […]

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June 28th, 2018

Endpoint Adjudication

George Clinical has a dedicated global endpoint adjudication team that delivers end-to-end services ranging from study development and set-up through to study close. Using a validated web-based endpoint management system, George Clinical manages endpoint adjudication activities to the highest scientific and operational standards. Specializing in cardiovascular and renal & metabolic endpoints, our endpoint adjudication team […]

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June 28th, 2018

Quality Management

George Clinical has a culture founded on Quality Management embedded across all our activities. Our Quality Management System facilitates a harmonized approach to the delivery and maintenance of quality and compliance which includes all the aspects in the following diagram: We work with you on your projects to comply with the Guideline for ICH Good […]

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June 28th, 2018

Medical Monitoring

George Clinical’s medical monitors come from diverse therapeutic backgrounds, and have the clinical and research expertise required to provide rigorous 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: Providing input into the study protocol, informed consent forms, project […]

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June 28th, 2018

Safety and Pharmacovigilance Services

George Clinical’s emphasis on employing strict safety reporting guidelines from the design stage of a trial ensures the quality and efficiency of our services and the safety of patients who participate in our trials. George Clinical’s safety and pharmacovigilance experts ensure that a patient’s safety is paramount. Critical to the success of any clinical trial […]

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June 28th, 2018

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