I need to track, trace and authenticate the product from the time it is initially sold to a distributor all the way through the supply chain to the point of distribution.
Counterfeiting medicines is a growing concern for public health and
safety. For this reason, every drug manufacturer is required to
serialize drug products at the item, case, and pallet level to
support the ability to generate a electronic pedigree (ePedigree)
document to track, trace and authenticate the product from the time
it is initially sold to a distributor all the way through the supply
chain to the point of distribution.
The drug e-pedigree standard provides the pharmaceutical industry
with a common format to collect pedigree information throughout the
supply chain. In the light of upcoming and existing laws that
require unique serialization and submission of electronic records to
supply chain partners pharmaceutical manufacturers need now to adapt
their IT Systems and business processes on time for compliance.
MAXLife simplifies and accelerates the ePedigree process from
receiving through shipment, simplifying compliance with government
regulations. With MAXLife, Life Sciences companies can:
- Simplify the creation and adoption of ePedigrees into the
supply chain
- Manage pedigree documents in a central, compliant
repository
- Manage Batch-Level Product Information
- Manage Distribution-Level Product Tracking
MAXLife for Microsoft Dynamics AX improves the ability to track
and trace products throughout the supply chain to protect public
health, and to shield a company’s brand from the damage of
counterfeiting.
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