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The Challenge:
Is your existing Autoclave or Pure
Steam Generator control system ..................?
- Old and difficult to operate
- Unreliable with no manufacturer support available
- Non-compliant with latest Regulatory requirements
- No alarm and event traceability
- Without user-security measures to prevent unauthorised
access to operator actions
- Built into inaccessible production and technical areas
making it difficult and/or expensive to replace
Upgrades also apply to other types of cGMP Equipment &
Systems including:-
Ovens, Purified Water Generation Systems,
Purified Water / WFI distribution systems and WFI Stills.
The Solution:
Upgrade to a compliant, fully validated Control System from
Honeyman Group Ltd, specialists in Pharmaceutical Process Support.
Our experienced Technical Team have successfully completed a
number of upgrade projects.
From Project initiation to completion and on-going support, Honeyman system
upgrades are benchmarked against 'Best in Class' and come with application
knowledge built in.
The Benefits
Improve Performance, Save Time, Upheaval & Cost
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| 1. |
PROJECT TIMESCALES CUT: |
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Typically reduced from 15 months
to just 3 months! |
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2. |
PRODUCTION
OUTAGE TIME DRAMATICALLY REDUCED: |
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Typically reduced from 6 months
to just 4 weeks!
No need for major re-building work or the upheaval of removing
redundant equipment. |
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3. |
SIGNIFICANTLY
LOWER COST: |
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You can typically save 20%
compared to the overall Project cost of replacement!
Not to mention the production down-time costs of such a project. |
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4. |
COMPLIANT TO
LATEST REGULATORY REQUIREMENTS: |
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Full GAMP and retrospective
equipment / systems validated to IQ and OQ. |
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5. |
FULLY
SUPPORTED: |
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Access to Honeyman Group's full range
of pharmaceutical process support services including process
validation, servicing, maintenance and on-going technical
support. |
The Features
- User-friendly operating methodology
- Bespoke presentation of operator user screens designed to
clearly depict the status of your application.
- Full traceability of operator actions, alarms, events and
parameter changes.
- Electronic records compliant with 21 CFR part 11 requirements.
- Optional Individual User ID and Password controls preventing
unauthorised equipment / system operation.
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