Released on = August 7, 2006, 10:50 am

Press Release Author = Mike Rozbih/ Novatek International

Industry =

Press Release Summary = Montreal - August 7th, 2006 - Novatek International, a world
leader that provides the Pharmaceutical, Biotech, Chemical, Biological, Contract and
Medical Device Industries a broad range of compliant specialized software solutions
today announced the latest version of its standardized Environmental Monitoring
software solution EM© version 2.1.

Press Release Body = Compliance has become mission critical for many organizations.
With the proliferation of regulations, such as 21 US Code of Federal Regulations
Part 11, cGMP, other international guidelines, and increased inspection from
internal & external auditing agencies, all aspects of a business are impacted.
Problems associated with microbiological environmental and utility monitoring data
control, documentation, reporting and trending are among those most commonly cited
as objectionable during FDA inspections of manufacturing facilities. As
pharmaceutical manufacturing sites strive to reach higher levels of process maturity
and compliancy, the movement towards adopting high-tech tools increases. Therefore,
an enforceable, clearly a process based complaint Environmental Monitoring solution
is crucial, no matter your size or industry.
"EM© version 2.1 is another confirmation of Novatek's consistent endeavors to look
in to the future of laboratory automation and the pharmaceutical industry's need for
specialized solutions," said Mike Rozbih, Senior Manager of Technical Sales &
Marketing, Novatek International.
Novatek International, the Environmental Monitoring solution' Power House, takes
pride in providing the pharmaceutical industry with the only process based
off-the-shelf, 21 CFR Part 11 compliant Environmental Monitoring solution. The
Environmental Monitoring solution EM© enables users to track and manage all
environmental & utility monitoring data for sterile and non-sterile health care
industries and other industries with a requirement for environmental monitoring
based on the latest guidelines from FDA, EU, ISO 14644-1 and PDA Technical report
13. It supports CFR Part 11 and other key regulatory requirements.

The Environmental Monitoring solution EM© offers complete off-the-shelf
environmental & utility monitoring workflows designed by some senior members of the
pharmaceutical and IT worlds such as Dr. Frank S Kohn ( President, FSK Associates &
a former Director of Wyeth, Vaccines) and Ms. Susan Cleary ( Associate Director of
Product Development, Novatek International). Additional EM© solution functionalities
allow companies to monitor locations, personnel and utilities for viable and
non-viable contamination as well as identify and track Micro-organisms. It includes
an enhanced Built-in statistics for rooms, personnel and utilities. It permits
location and personnel mapping, execution of investigations for incidents such as
"OOS" conditions, management of media and inventory for cost effective operations
and configurable reporting & query tools for data retrieval, control and knowledge
management.


Novatek International EM© Contact:
Mike Rozbih
(+) 1.514.337.7337
Mike.Rozbih@ntint.com



Web Site = http://

Contact Details = Novatek Intl
5995 Gouin Blvd West, Suite 308
Montreal, QC, Canada
Mike Rozbih
Corporate Manager, Technical Sales & Marketing
Novatek International
Tel: (514) 337-7337
Fax:(514) 336-6537
E-Mail: Mike.Rozbih@ntint.com