Running an efficient,
compliant manufacturing and distribution operation
is no small challenge with the detailed QA documentation
and pedigree documentation that’s required
throughout the drug production, packaging and distribution
process. And the threats posed by drug counterfeiters
only add to management’s headaches.
Standard Register provides a wide of array of
solutions to assist pharmaceutical companies
in bringing greater productivity and security
to the production and distribution environment.
With deep expertise in business process management,
document security and label solutions, we can
help you introduce greater efficiencies and control
to your operations while tightening the reins
on costs.
QA Documentation & Pedigree
Documentation Whether your documentation
processes are paper-based, digitized or somewhere
in between, Standard Register can assist you
in organizing, managing and migrating your
document systems to a new level of efficiency.
We’ll analyze your documents and processes
to identify opportunities for improvement and
develop a plan to streamline the process. Then
we’ll work with you to implement a customized
solution, training your people and helping
you make a seamless transition.
Standard Register can be a valued ally, particularly
now, as you begin to consider how you will meet
recommendations of the new FDA counterfeit drug
initiative. We can help you map a plan that takes
advantage of today’s bar codes and secure
technologies to help improve the integrity of
your drug supply chain now and ultimately transition
to RF technology as it becomes viable.
To learn more about how we support QA
and Pedigree Documentation, click here.
Secure Document & Label
Solutions A leader in secure document
technologies, Standard Register can help you
minimize opportunities for fraud. With a well-designed
set of features integrated into vital documents,
and the proper procedures and system controls
in place, we can help you enhance the integrity
of your QA and pedigree documentation processes.
These same technologies can be applied to produce
tamper-resistant labels to support your packaging
operation. By combining innovative design with
the right substrate, our experienced label solutions
team can address highly specialized requirements:
- Secure product labels
- Tuck labels
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- Temperature-sensitive labels
- Dissolvable labels
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Learn more about Secure
Document and Label Solutions now.
Bar Code Automation Standard
Register brings together the best thinking and
bar code technologies to automate documentation
processes and help you realize the benefits of
the FDA’s 21 CFR Part 11 ruling. We work
with you to streamline workflow, procedures and
systems, designing a solution to fit your operations
and help address regulatory requirements. We
can be your single source for labels, forms and
supplies, hardware and software, integration
and implementation services in addition to technical
support and on-site service.
In addition to bar codes, we are also leveraging
digital technologies to introduce a new level
of efficiency and control. Consider our digital
pen and paper technology, for example. Currently
in pilot testing, this innovative, mobile technology
captures information as it is handwritten and
converts it into a digital format, feeding it
to backend systems. With its ability to time-stamp
entries on forms while validating and authenticating
signatures, it could be valuable in bringing
greater control to documentation processes. Learn
more about Document
Automation solutions now.
Bar Code Solutions
for FDA Mandate Standard Register is
ready to assist you in meeting the FDA’s
recent mandate to bar code most prescription
drugs and certain over-the-counter drugs to
give hospitals a quick, efficient way to check
medications and dosages. With our technology
expertise and leadership in healthcare solutions,
we’re uniquely positioned to help you
address both your requirements and those of
your end-users. Contact us today to begin discussing
how you can meet the new FDA
bar code label requirement for human drug
products and blood.
Label Inventory
Management Standard Register offers
a Web-based Label Management Inventory System™ (LMIS)
to help streamline replenishment of product,
compliance and shipping labels through MRP
demand flow or min-max scenarios. Linking directly
to our in-house systems, LMIS lets us know
immediately when to reorder, print and ship
label products. Moreover, with 24/7 access
to real-time reports on label usage, inventory,
pending orders and shipments, users can effectively
manage and control the labels, vital to supply
chain management. LMIS is a powerful management
tool. Secure more information now about how
you can use LMIS to
drive down procurement and inventory costs
while facilitating just-in-time delivery.
Packing & Shipping
Solutions Standard Register will apply
its technologies and expertise to challenges
in your packing and shipping operation as well.
A notable example of our cost-effective solutions
is Pack List Express™.
Pack List Express is an innovative solution
that does away with separate packing lists and
envelopes, replacing them with one label that
can be designed for one or two-sided printing.
If you want to truly optimize packing operation,
you can use a duplex printer and combine the
shipping label and packing list into a single
document, thereby reducing errors, processing
time and costs. Then by fully automating the
process, you can gain even further efficiency.
Whichever approach you prefer, we’ll work
with you to tailor it to your needs. Contact
us now to secure more information about Pack
List Express.
Related Information & Links
FDA Bar Code Label
Requirement for Human Drug Products and Blood
www.fda.gov/bbs/topics/news/2004/hhs_022504.html
Combating Counterfeit Drugs, FDA Report, February
2004
www.fda.gov/oc/initiatives/counterfeit/report02_04.html#execsummary
Healthcare Distribution
Management Association
www.healthcaredistribution.org |
