Our network of global manufacturing facilities ensures support for Customers worldwide. They are situated in Ireland, United States, Poland and Malaysia. The four unified state-of-the-art facilities offer solutions on all continents.
IRELAND
SteriPack HQ Ireland
Established: 2017
Facility features: 10.500 Sqm, 2.000 Sqm ISO Class 7 clean room
Capabilities: Headquarters, Science & Innovation Campus & Plant, Technical Centre, Administration, Clean room Additive / 3D Printing (Polymers & Elastomers), Clean room Manufacturing
POLAND
SteriPack Poland
Established: 2006
Facility features: 15.000 Sqm, 2.300 Sqm ISO Class 7 & 8, Grade D clean room , ISO 13485 / ISO 17025 / cGMP
Capabilities: Full Range of Contract Services from Development to Final Product, Clean room Injection Moulding, Manual to Automated Assembly, Kitting & Packing, Development & Project Management, Secondary Pharmaceutical Packing, ISO 17025 Accredited In-House Microbiological Laboratory
USA
SteriPack USA
Established: 2012
Facility features: 3.900 Sqm, 1.800 Sqm ISO Class 8 Clean room, ISO 13485
Capabilities: Full Range of Contract Services from Development to Final Product, Clean room Injection Moulding, Manual to Automated Assembly, Kitting & Packing, Development & Project Management
MALAYSIA
SteriPack Malaysia
Established: 2007
Facility features: 8.000 Sqm, 2.230 Sqm ISO Class 8 clean room , 540 Sqm Grade D clean room , ISO 13485 / cGMP
Capabilities: Full Range of Contract Services from Development to Final Product, Clean room Injection Moulding, Manual to Automated Assembly, Kitting & Packing, Development & Project Management, Primary & Secondary Pharmaceutical Packing
USA
HS Design, Inc.
Established: 1979
Capabilities:
Design Research & Human Factors, Industrial Design, User Experience, Mechanical Engineering, FEA/CFD analysis, Electrical Engineering, Software Engineering, Rapid and Pilot Prototyping, Technology and Manufacturing Transfer
IRELAND
Europharma Concepts Ltd. Ireland
Established: 2007
Facility features: 2,300 Sqm, 1.100 Sqm ISO Class 8 clean room, ISO 13485 / ISO 22716
Capabilities:
Fluid Filled Medical Devices, Contract Services, Research, Formulation, Product Design, Development & Process Validation, Testing, Supply Chain Management, Packaging, Sterilization Management
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