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3/2010:
SmartSupplies LDP 1.0.0 (Label Design and Printing) commercially released. |
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3/2010:
Clinapps to attend Midwest Clinical Supplies Group Annual Meeting March 21-24 in San Antonio, TX |
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1/2010: SmartSupplies PMD 5.0.0 Commercially released and featuring ability to print customized bar-code labels, inventory receipts and more. |
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| Home >
Products > SmartSupplies PMD (Planning Materials Distribution) |
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For More Information Click Here To send an email request.
CLINapps Inc. is pleased to announce the release of SmartSupplies PMD 5.0.0.
This easy to use, fully web enabled
solution empowers Biotechnology and Pharmaceutical organizations of all sizes to effectively Plan, Monitor and Control the clinical supplies process.
CLINapps’ SmartSupplies PMD solution provides a protocol driven framework coupled with bi-directional integration to manufacturing systems
(ERP), IVR services and B2B partners. With SmartSupplies PMD, Clinical protocol requirements are translated into accurately packaged and
distributed investigational drug products. SmartSupplies PMD is designed to dramatically increase the efficiency, accuracy and compliance of the
clinical supply process with immediate benefits including:
| Planning |
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Clinical Protocol Driven Framework |
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Easily design and capture complex protocol stratifications |
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Supports all study types and randomization methods |
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Model subject kits and ancillary supplies |
| Manufacturing |
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Design multi-level subject kits and Bill of Materials |
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Supports blinded materials |
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Create and track Manufacturing Requests |
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Allocate lots to one or more Manufacturing Requests |
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Pool materials across multiple studies |
| Packaging and Distribution |
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Management of internal and external packaging efforts |
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Submit, approve and track shipment requests |
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Execute manual and IVR initiated shipment requests |
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Prevents distribution to unauthorized sites or countries |
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Prevents distribution of non-released materials |
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Monitor shipping status online |
| Management & Control |
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Subject Kit Level granularity |
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cGMP and 21 CFR Part 11 compliant |
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Regulatory Control to prevent distribution to unauthorized sites or countries |
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Effective management of clinical programs, studies, investigational sites and investigators |
| Integration & Communication |
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Integrates to ERP Systems, IVR Services and B2B Partners |
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Provides Unified, Single Reference between departments, investigational sites and B2B partners |
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For More Information Click Here To send an email request.
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