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Validation and Compliance Consulting
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With increasing regulatory
scrutiny and requirements to
comply with national and
international regulations,
more and more companies are
moving to replace manual and
paper-based processes with
automated systems. Due to
their experience and
background, CSI consultants
are well equipped to qualify
your systems of varying
levels of complexity and
help you stay compliant. CSI
optimizes the time and cost
of validation by applying a
risk-based approach to each
system. CSI can also provide
a wide range of automated
tools as part of the
consulting engagement to
provide you with sustainable
compliance.
CSI is a recognized leader
in providing compliance
solutions to the
FDA-regulated industry with
a global client base that
spans North America, Europe
and Asia. CSI consultants
combine regulatory knowledge
with technical expertise to
provide solutions to issues
instead of simply
highlighting them. CSI
follows the FDA-recommended
GAMP 4 methodology for all
validation services. CSI's
validation methodologies
have been developed after
years of real-world field
experience to ensure
successful project outcomes.
We strive to deliver value
as an added ingredient in
all our deliverables with a
view to improving operations
and productivity and
simplifying processes with
compliance as a by-product.
CSI offers a wide range of
services that include
validation planning, risk
assessments, Part 11
assessments and remediation
plans, preparation of
validation documents and
SOPs, protocol execution,
deviation resolution and
training. CSI regularly
contributes to industry
conferences, journals,
tradeshows and events and is
in tune with current FDA
thinking and future
direction. |
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Computer Systems Validation
Experience - Representative
Systems |
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Enterprise Resource Planning
(ERP) Systems |
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Laboratory Information
Management System (LIMS) |
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Document Management Systems
(DMS) |
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Adverse Event Systems |
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Network Infrastructure
Qualification |
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Laboratory Systems |
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Spreadsheet Validation |
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Plant Floor Systems |
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Equipment/Systems Validation |
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Label Management Systems |
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Manufacturing Execution
Systems (MES) |
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Clinical Trial Management
Systems |
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Source Code Reviews |
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Change Management Systems |
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Batch/Process Data
Management System |
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Database Querying and
Information Retrieval in a
Controlled, Part 11
Environment |
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Computerized Maintenance
Management Systems |
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Engineering Drawing
Management System |
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Environmental Monitoring and
Trending |
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Training Systems |
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Our Key Differentiators: |
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Experience |
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People |
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Methodology |
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Industry Participation |
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Regulatory Knowledge |
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© Copyright
2000-2008. CIMCON Software, Inc. All rights reserved. |
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