POMS
CMS™ for Clinical Supplies  Manufacturing
Compliance, Speed and Efficiency for Clinical
Manufacturing and Supplies
When you are bringing a new pharmaceutical product
to market, delay caused by inefficiencies, and incomplete
or lost records can translate into a loss of millions
of dollars. Prices pharmaceutical companies charge are
enduring increased scrutiny from Regulatory agencies,
public interest groups and the newsmedia. Cost
controls are increasingly a way of life for R&D.
To compete in todays fast-paced marketplace, you must
strive to reduce time-to-market, control the rising
cost of drug development, increase compliance efficiency,
and achieve earlier attainment of revenues associated
with the drug.
Honeywell’s POMS CMS™ is an ideal tool
to help achieve these objectives. POMS CMS™ is
a clinical manufacturing and supplies (CMS) system that
directs and enforces current Good Manufacturing Practices
(cGMP) and streamlines specification, production, packaging,
labeling, and distribution of clinical supplies.
Since all POMS records are electronic, the software
also simplifies the transfer of formulation histories
and master batch records to commercial production.
The result is faster new drug application (NDA) preparation
and new product scale-up.
POMS CMS Benefits
• Reduced time-to-market
• Reduced development costs
• Ensured compliance with regulations
• Streamlined new drug application activities
• Faster scale-up to commercial production
Versatility for the Spectrum of Operations
POMS CMS supports and enforces the procedures and functions
required by drug development organizations in the specification,
production, management and distribution of clinical
supplies.
The application increases a clinical organization’s
ability to respond to medical and study tests, while
reducing waste, lowering costs, and ensuring compliance.
You have the assurance the right clinical supplies are
produced, tracked and delivered to the right investigation
site.
The system’s versatility is ideal for small,
constantly changing batches; production volumes; and
packaging requirements unique to clinical supplies.
POMS CMS also reduces time-to-market by streamlining
new drug approval preparation activities, and accelerates
the transition to commercial production volumes by seamlessly
integrating with the POMS MES™ manufacturing execution
system.
POMS CMS Functionality
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