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In the construction
or restructuring of chemical and pharmaceutical production
plants, GMP starts at the very beginning of the design
phase.
Our Offer
Take advantage of our many years of experience in:
- User Requirement Specification (URS)
- Plant concepts
- Selection and evaluation of plant components
- CIP / SIP technology
- Clean-room technology
- Water producing plants
- And much more
Our Procedure
Together with you and our engineering partners we define
the procedure to reach "integrated plant qualification"
at the beginning of each new construction or restructuring
project. The main focus is on the adaptation to standard
engineering procedures as well as to your specific procedures
to make the work as efficient and cost effective as
possible.
Especially during Design Qualification
(DQ) we support you in the development of GMP- oriented
studies and user requirement specifications, we help
with advice in the selection and evaluation of specific
plant components and give recommendations and tips in
the selection of suitable suppliers.
Through project meetings with engineers,
subcontractors and suppliers at the very beginning of
the project we ensure that quality-relevant specification
criteria are followed and the documents necessary for
qualification are provided in time.
For the detail engineering stage we place
at your disposal process engineers, electrical engineers,
construction engineers and experts who can instigate
the most important GMP requirements into the design
phase of the plant.
Your Result
User Requirement Specification (URS), plant concepts
and technical solutions in accordance with GMP requirements
that support the qualification and validation activities
in all points.
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Consulting
