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IMP MANAGEMENT

Develop Clinical Trial Supply Plan

Authorize study product shipment to sites

IMP management (storage in Local Depot, tracking)

IMP drug accountability

IMP reconciliation/return from clinical sites/destruction at Clinical Sites

Distribute Clinical non-study drug supplies to sites, including replenishment orders

Monitor Clinical (Study Drug) non-clinical (non-study drug) supplies and accountability at sites

Contact us

For any questions you have, you can reach us here:

Tina Landess

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2532 Santa Clara Ave, Suite 344

Alameda, CA 94501

United States

admin@landrichgroup.com

+1 510.912.2589

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