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Research supplier
University of Massachusetts Medical School - Investigational Drug Service Core
University of Massachusetts Medical School - Investigational Drug Service Core is listed as an academic core research supplier in the Scientist.com network, with 1 site in 1 country.
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Logo UMasswebteam, via Wikimedia Commons, CC BY-SA 4.0. Shown to identify the organization; it may be a registered trademark.
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Academic core
No service areas are recorded for this supplier yet.
Where it operates
Sites by country, with the cities in each.
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United States 1 site
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
The investigational pharmacists play a key role in facilitating subject safety for clinical trials being conducted at UMass and UMass Memorial. Staffed with 2 (two) full-time pharmacists, the IDS have the following major responsibilities as defined in UMass policy: Preparation of IDDF (drug data form) for review by IRB committee Assessment of appropriate charges for investigational services Receipt, storage, accountability, dispensing and return/destruction of all investigational drugs Monitoring of all ongoing investigational drug activity by clinical researchers in the medical...
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The investigational pharmacists play a key role in facilitating subject safety for clinical trials being conducted at UMass and UMass Memorial. Staffed with 2 (two) full-time pharmacists, the IDS have the following major responsibilities as defined in UMass policy:
Preparation of IDDF (drug data form) for review by IRB committee
Assessment of appropriate charges for investigational services
Receipt, storage, accountability, dispensing and return/destruction of all investigational drugs
Monitoring of all ongoing investigational drug activity by clinical researchers in the medical school or on the campuses of UMass Memorial Medical Center
Control and accountability of investigational drugs according to state and federal regulatory requirements, sponsor specifications and hospital pharmacy practice
Consultation with investigators pre-study and throughout conduct of trial
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