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The Clinical Trial Supply chain: Best practice to ensure ... - Almac

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INVENTORY<br />

SYSTEM<br />

VENDOR<br />

INVENTORY<br />

IVRS<br />

SITE/ DEPOT<br />

INVENTORY<br />

BULK<br />

DRUG<br />

MATERIALS<br />

STUDY KITS<br />

SUPPLY<br />

STRATEGIES<br />

STOCK LEVELS<br />

MATERIALS<br />

STUDY KITS<br />

Data integration layer<br />

Reports – au<strong>to</strong>mated supply management<br />

Figure 2- future data standardisation allowing au<strong>to</strong>mated supply <strong>chain</strong> integration<br />

More efficient and effective clinical trials?<br />

Sponsor companies can assist the clinical trial supply departments both within their<br />

own company and outsourcing partners, by planning ahead and giving some visibility<br />

<strong>to</strong> the drug development plans. This will assist in management of demand forecasting<br />

and capacity, and also identify potential problems in advance.<br />

Further use of technology <strong>to</strong> control and manage various parts of the clinical supply<br />

<strong>chain</strong> means that data integration needs will grow within the industry. Organisations<br />

will strive <strong>to</strong> focus not only on operational expertise, but also on the ability <strong>to</strong><br />

integrate in<strong>to</strong> set data standards that allow them <strong>to</strong> take their place in an integrated<br />

supply <strong>chain</strong>.<br />

Jonathan Calderwood<br />

Global Marketing Manager<br />

<strong>Almac</strong> <strong>Clinical</strong> Services, Craigavon, UK<br />

Tel: +4428 3836 2436 Fax: +4428 3836 3623<br />

E-mail: jonathan.calderwood@almacgroup.com

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