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Capacity doubled without delay for GMP-compliant pharma plant


When Pronova BioPharma needed a facilities upgrade with minimum downtime, the company called on NNE Pharmaplan. The result was a GMP-compliant production plant with doubled capacity and fast-tracked resumption of production.

Pronova BioPharma is a global leader in the research, development and manufacture of marine-originated omega-3 derived pharmaceutical products. The company’s lead product is manufactured at its plant in Norway using a complex proprietary process.

Having experienced strong growth over the past three years, with demand increasing for its active pharmaceutical ingredient (API), the company decided to open a second manufacturing site in Denmark.

Meeting increasing demand with minimum downtime
The project needed to be approached as a “pit stop” project – with a short shutdown period and a fast-tracked resumption of updated production when the shutdown was over.

NNE Pharmaplan provided a complete range of services, from conceptual design to construction management and qualification. This also included a new distillation unit, a DeltaV automation upgrade on the existing distillation unit, a GMP upgrade on parts of the units and much more.

The results have been a doubling of production capacity with minimum of down periods. Pronova BioPharma can now continue to meet demand for its innovative pharmaceutical ingredients.

 

 

Got questions?

Henning Brink Haltrup
General Manager, Ireland


Tel+353 1 6628908

facts


Client
Pronova BioPharma AS, Norway
Client's success factors
Fast-track upgrade of new facility, production capacity increase, GMP compliance
Project duration
Jan. 2006 – Sep. 2007
Service provided
Basic design
Detail design
Control system – functional requirement specifications
Control system (Emerson Delta V) – programming & computer validation
Construction management
Project management
Installation and commissioning supervision
Qualification


NNE Pharmaplan 2008
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