Contact Information: AT SCHAWK, INC. Alex Sarkisian (847) 827-9494 asarkisian@schawk.com AT SCHAWK, INC. Stephen Kaufman (312) 666-9200 skaufman@schawk.com FOR SCHAWK, INC. Patti Soldavini (973) 527-8103 patti.soldavini@schawk.com
Schawk Digital Solutions Makes Its Pharma-Grade Software Validation Package Available to Food and Beverage Industry
Designed to Mitigate Risk Surrounding Growing Food Safety Regulation
| Source: Schawk, Inc.
DES PLAINES, IL--(Marketwire - September 17, 2009) - Schawk, Inc. (NYSE : SGK ), a leading
provider of brand point management services enabling companies of all sizes
to connect their brands with consumers to create deeper brand affinity,
announced today that it is making its pharma-grade software validation
package available to the food and beverage industry.
This comprehensive software validation package, which allows for the
controlled implementation of Schawk's BLUE™ software has been designed
to meet the highest levels of quality management standards within highly
regulated and validated environments. Schawk has been delivering fully
configurable, comprehensive software and validation service solutions to
seven pharmaceutical and medical device companies worldwide since 2002. As
Schawk has been helping the pharmaceutical and life sciences industry
mitigate risks associated with mis-labeling, documentation and
traceability, it can help consumer products companies mitigate similar
risks surrounding growing food safety regulation.
Alex Sarkisian, chief operating officer, stated, "In a global economy where
ingredients may be sourced in one part of the world for products
manufactured and packaged in another part of the world, food safety must be
viewed through a global prism. All consumer products companies --
especially food and beverage companies -- will have a greater obligation to
comply with growing regulatory oversight, inspections and audits to trace
the source and distribution of products from source to shelf."
According to David A. Schawk, president and chief executive officer,
"Schawk's experience delivering validated solutions to the rigorously
regulated pharmaceutical and life sciences industry can be leveraged by
food and beverage companies to get ahead of the legislative curve, as
opposed to reacting under pressure to required compliance measures. These
measures could occur with more frequent inspections as a result of the
recent passage of H.R. 2749, the Food Safety Enhancement Act of 2009."
Schawk's software validation package is supported by strict quality
management standards. Schawk Digital Solutions adheres to predefined System
Implementation Life Cycle (SILC) procedures which allow for the controlled
implementation of its BLUE software. Each SILC procedure lays out step by
step, the requirements necessary to plan, design, build, test, train and
deploy a BLUE system, and articulates the outputs and deliverables for each
stage.
Stephen Kaufman, chief technology officer, commented, "Schawk's validation
package is designed to help clients efficiently achieve compliance while
working within their internal standard operating procedures to satisfy
compliance with both internal policies and FDA guidance documentation
requirements. If a company is already using Schawk's BLUE software, like
many food and beverage companies are, they are already ahead of the game.
Our quality management documentation for non-validated environments is
exceptionally strong, permitting an easy transition to a validated
environment for most companies."
The Schawk validation package consists of detailed templates containing
SILC information that may be used by food and beverage companies to produce
the documents required by the U.S. Food and Drug Administration (FDA).
These templates have been created against validation industry guidelines
and include various key validation planning and reporting documents,
requirements and design documents and qualification protocols.
The implementation of BLUE within a highly regulated, validated environment
also enables companies to comply with Title 21 CFR Part 11 of the Code of
Federal Regulations which encompasses the U.S. FDA's guidelines on
electronic records and electronic signatures in the U.S.. CFR Part 11
defines the criteria under which electronic records and electronic
signatures are considered to be trustworthy, reliable and equivalent to
paper records. It also requires drug makers, medical device manufacturers,
biotech companies and other FDA-regulated industries to implement controls,
including audits, system validations, audit trails, electronic signatures
and documentation for software and systems involved in processing
electronic data as required by FDA regulation.
Additionally, Schawk is accustomed to working within the regulations
required of a cGMP-compliant (current Good manufacturing Practices)
environment and is a certified supplier to clients working within this
environment. This certification provides for systems that assure proper
design, monitoring, and control of manufacturing processes and
facilities. When adequately put into practice, GMPs help to prevent
instances of contamination, mix-ups, deviations, failures, and errors
related to the manufacture and labeling of products.
Because packaging and labeling falls under FDA guidelines, quality auditors
use FDA guidelines on manufacturing to inspect the facilities of their
certified suppliers. As part of comprehensive, routine inspections, quality
auditors inspect Schawk's processes surrounding the intake, application,
documentation, change management and tracking of information related to
labeling and packaging. Some of the checkpoints that these auditors inspect
relate to making sure the instructions on labeling/packaging are easy to
read, the dosage instructions are correct, the content of the product
matches the ingredients on the label and the size of packaging is correct
based on the dosage.
BLUE is Schawk's proprietary enterprise brand management software developed
specifically to guide the lifecycle processes of the packaging and
promotional materials developed to market, promote and deliver brand
experiences. Schawk supplements its brand management technology with
consulting, installation, training and maintenance and can provide on-site
manpower when required. BLUE is comprised of five web-accessible modules
that encompass digital asset management, copy management, workflow
management, online proofing (which includes annotation and comparator
tools) and Key Performance Indicators, or KPI, reporting. These integrate
seamlessly together and with company-wide Enterprise Resource Planning
(ERP) systems, and can be responsive to the complexities and unique
requirements that regulate packaging in ways that broad-based ERP systems
do not. BLUE is part of Schawk's brand point management offering. Schawk
helps companies create compelling and consistent brand experiences by
providing integrated strategic, creative and executional services across
brand touchpoints at home, on the go, at the store and on the shelf.
Schawk, Inc. is the leading provider of brand management services, enabling
companies of all sizes to connect their brands with consumers to create
deeper brand affinity. With a global footprint of 49 offices, Schawk helps
companies create compelling and consistent brand experiences by providing
integrated strategic, creative and executional services across brand touch
points. Founded in 1953, Schawk is trusted by many of the world's leading
organizations to help them achieve global brand consistency. For more
information about Schawk, visit http://www.schawk.com