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DPS
Engineering & Construction Ltd.– The Company
Formed in 1974, DPS is now a leading Engineering and Project
Management Company in the Pharmaceutical Industry. We employ over
250 people in our 3 European Offices and serve a broad range of
clients ranging from Multinational companies to small Generic
Producers. DPS is fully owned by its working directors which ensures
a personal approach, to project ownership and high level commitment
which sets us apart from our competition.
DPS is totally dedicated to the Pharmaceutical sector. Our focus
is on quality, meeting the clients business needs, being responsive
and flexible and maintaining long term client relationships. Our
Size and Multi-national Presence allow us to execute projects
both small and large in many locations.
Our Mission
DPS Engineering will remain Dedicated to the Pharmaceutical Market,
targeting revenue from the capital projects, operational budgets
and R&D expenditures for existing and new pharmaceutical facilities
and building our future on a reputation for technical and service
excellence.
Business Sectors
- Dedicated to the Pharmaceutical Industry
- Full Project Execution Capability (EPCMV)
- Site Selection & Master Planning
- Feasibility / Conceptual / Front End Studies
- Construction Management & Commissioning
- Validation Execution (DQ,IQ,OQ,PQ support)
- High Level Project Evaluations/ Review
- Contract Services/ Client Teams
Bulk Pharmaceuticals
Our Process capability in Pharmaceutical
Bulk Manufacture ranges from Pilot Plant and scale-up through
Synthetic and Biological steps to Purification Isolation and final
API Handling. We have particular skills in the later stages of
Product Containment, cGMP and Operator Protection derived from
our experience in Secondary Manufacture. Similarly, we have excellent
experience in Contained Solids Handling. We were selected by GlaxoSmithkline
and Pfizer for significant GMP upgrades in this specialist area
in recent years. Safety and Hazard Analyses are key parts of our
design process and compliance with both Safety and Environmental
regulations are fundamental in our approach. Our capability in
Bulk Facilities covers Conceptual Design, Detailed Engineering,
Procurement, Construction Management, Commissioning and Validation
and many of our facilities have successfully undergone FDA audits.
Secondary Pharmaceuticals
Design, Construction and Validation of Secondary facilities
for the full range of dosage forms has been a central part of
DPS activity for over 15 years. Our clients have ranged from Multinational
Producers to small Generic Operations, and our experience has
covered Oral, Topical, Parental and other dosage forms. Most of
our projects in the Secondary area begin with conceptual design
and we have considerable experience in Layouts, Materials and
Personnel Flows, Access Requirements as well as Material Handling,
Containment, Cleanroom Design and Sterility. All our Engineering
Staff have been imbued with a Pharmaceutical Culture and the careful
detailing of interdisciplinary interfaces is a particular speciality.
Our Secondaries capability includes expertise in Equipment Specification
and Procurement for both Oral and Parental Processing as well
as the interdisciplinary skills required for facility design.
Our Validation experience includes direct dealing with FDA and
other National Regulatory Bodies.
Biopharmaceuticals
Expertise in Sterile Processing for Parentals Manufacture and
a long term involvement in conventional fermentation were the
foundation for DPS current Biopharmaceutical capability. Our experience
spans all stages of manufacture from Laboratory scale, through
full production facilities, and our process team includes highly
qualified Microbiologists, Biochemists and Biochemical Engineers
to support our other engineering disciplines in executing Biopharmaceutical
projects. Our process know-how covers the full range of specialised
equipment from Inoculum preparation, through Fermentation &
Downstream Processing to final formulation, Aseptic filling &
Freeze Drying. Strong capabilities in cGMP design & Biohazard
containment ensure regulatory compliance & effective integration
of these requirements in cost effective and functional layouts.
The critical requirements for cleaning and sterilisation are central
to our Biopharmaceutical design approach and automated CIP/SIP
systems are our speciality, as are the "Clean" utilities
needed to support Biopharmaceutical manufacture.
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Us
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Address
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DPS Engineering & Construction
Ltd. |
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4 Eastgate Avenue
Eastgate Business Park
Little Island
Cork
Ireland |
| Tel. |
+353 21 450 33 22 |
| Fax |
+353 21 450 35 27 |
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