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RFQ: MIC 2022 006: SUPPLY AND DELIVERY OF A WATER CHILLER AT ANATOMICAL PATHOLOGY; CMJAHREQUEST FOR QUOTATIONDESCRIPTION: RFQ: MIC 2022 006: SUPPLY AND DELIVERY OF A WATER CHILLER AT ANATOMICAL PATHOLOGY;
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01
Determine the specific requirements and timeline for the clinical trial supply.
02
Coordinate with relevant stakeholders including the study team, regulatory authorities, and suppliers.
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Prepare and submit necessary documentation for approval of the clinical trial supply.
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Procure all necessary materials and ensure timely delivery to the study sites.
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Who needs clinical trial supply east?

01
Pharmaceutical companies conducting clinical trials
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Research institutions and academic centers
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Contract research organizations (CROs) managing clinical trials
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Clinical trial supply east is the process of providing pharmaceutical products and medical devices to participants in a clinical trial.
The sponsor or investigator of the clinical trial is required to file the clinical trial supply east.
To fill out clinical trial supply east, the sponsor or investigator must provide detailed information about the pharmaceutical products and medical devices being used in the trial.
The purpose of clinical trial supply east is to ensure that participants in a clinical trial receive the necessary pharmaceutical products and medical devices in a timely manner.
The information reported on clinical trial supply east must include details about the pharmaceutical products and medical devices being used, as well as information about the dosing regimen and storage requirements.
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