Monitoring

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Our team is skilled in clinical trials management and monitoring, including traditional on-site and remote monitoring, in addition to risk-based and adaptive approaches. We ensure that findings and action items are addressed promptly and entirely, enabling effective and efficient work flow.


Ensuring high performance and quality of the clinical trial in accordance with GCP, local regulations, SOPs and the study protocol. Our staff handle all aspects of the trial from feasibility and site selection, through startup and recruitment, until trial completion.


Our project managers and CRAs provide an umbrella service to our clients with one point of contact throughout the project, facilitating clear communication.


We make certain that the trial is conducted according to plan, within established timelines and budget, while producing high quality data.

Regulatory Affairs

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Q-Trials implements a strategic approach to obtain approvals from the local ethics committee, central ethics committee where applicable and Ministry of Health (CA).


We have a deep understanding of the regulatory environment in Israel and can shorten the start-up phase.

Logistics

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Q-Trials offers importer of records services, storage and delivery for medical device and study materials such as lab kits, ECG, glucometers, and other study supplies.


Q-Trials also serves as a liaison with local drug depots, supporting labeling and dispatch. We arrange for local accountability, re-labeling, collection and destruction from sites as well as temperature controlled patient home deliveries, .

Translations

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Other

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