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Scaleable, high-performance records-management
solutions are now the affordable alternative to inflexible and expensive
DMS and ERP systems for pharmaceutical and biotech market
June 13, 2005 - Vienna, VA - ZyLAB, an innovative
developer of content management and compliance solutions for paper
intensive organizations, today announced the availability of its
new FDA-compliant content-management solution for the pharmaceutical
and biotechnology industries. In most cases, not only will the ZyLAB
FDA-compliant solution cost up to a third less than other comparable
systems, but it will take a fraction of the time to deploy.
ZyLAB has bundled the technology required by leading firms into
a standard, scaleable ZyIMAGE-based system that contains the most
advanced tooling available, on a scale that is flexible for specific
organizational needs. This mix of scalability and functionality
is proving to be a successful strategy for ZyLAB in its continued
penetration of the pharmaceutical and biotechnology records-management
market, particularly in terms of providing enhanced value for money.
Most importantly, ZyLAB's ZyIMAGE pharmaceutical and biotechnology
solution is completely aligned with rigid FDA guidelines for records
management.
The ZyIMAGE solution is used for digital capture and archiving of
lifecycle GMP records, as well as all paper records requiring back
up, such as validation protocols, validation reports and batch records.
This ZyIMAGE solution also controls document review and access through
a specialized interface or web browser, while maintaining a full
audit trail of all actions performed. Many of ZyLAB's clients in
this market are able to adapt and implement the ZyIMAGE solution
in numerous departments across the entire firm, such as R&D,
engineering, manufacturing, quality control, distribution, and global
operations.
Of course, any ZyIMAGE solution includes standard core ZyIMAGE
features such as fuzzy search, hit navigation and highlighting,
no additional plug-ins, tools for publishing archives to CD or DVD,
and more. These capabilities have always formed one of the most
attractive tool suites for organizations that are required to adhere
to a variety of regulations and rigid business practices, as well
as remaining vigilant against fraud. In fact, most Federal and private-sector
regulators rely on ZyLAB software to help conduct their audits and
investigations.
In accordance with FDA guidelines, the audit trails utilized by
this ZyIMAGE solution for relevant actions is fully compliant with
21 CFR Part 11. Full documentation has been prepared and approved
for the ZyIMAGE solution.
About ZyLAB
Founded in 1983, ZyLAB is the leading provider of low-cost content
management and compliance solutions for small-and-medium-sized business
(SMB) and government organizations that need to digitally file and
manage millions of pages of paper and electronic documents. ZyLAB's
comprehensive investigative capabilities, with its high quality
search and retrieval features supporting over 200 languages, gives
users the ability to organize and easily share all information online.
In particular, ZyLAB solutions are relied upon extensively by legal,
law enforcement/intelligence, and financial/back-office professionals.
With over 7,500 installations worldwide and over 350,000 users, ZyLAB
has a wide breadth of experience and knowledge across a variety of
different industries and business applications. Our clients include
such U.S. Government organizations as the FBI, Department of Homeland
Security, Department of the Treasury, Department of Justice, SEC,
Department of Agriculture, Department of Commerce, IRS, Department
of Labor, State Department, Amtrak's OIG, Office of Personnel Management,
Department of Defense and all branches of the US military, as well
as such well-known companies as the New York Stock Exchange, Pepsico,
Pacific Life, and Anheuser-Busch. For more information visit: www.zylab.com - contract management.
Media Contact:
Evan Weisel
Welz & Weisel Communications
P: 703-323-6006
evan@w2comm.com
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