Today’s operating and business climate demands facilities that provide flexibility and adaptability to accommodate dynamic and increasingly complex market requirements.
As the industry advances, the need for controlled environments, efficiency and validated up-to-date facilties continues to be a primary focus; Austin’s understanding of the pharmaceutical industry makes it uniquely qualified to provide facilities that meet manufacturers’ short and long term objectives.
Within the field of pharmaceuticals, Austin designs and constructs:
- Research and development centres
- Pilot and scale-up plants
- Clinical trial and quality control buildings
- Bulk and intermediate manufacturing plants
- Secondary production facilites
- Finishing and packaging plants
- Distribution centres
Austin has extensive experience in planning and implementing facilities for all types and classes of products including capsules, tablets, powders, injectables, creams, ointments, liquids and creams.
Austin understands the requirements of Medicines and Health Care Products Regulatory Agency (MHRA), Food and Drug Administration (FDA) including the design of Clean Rooms to ISO6/Class 1,000, ISO7/Class 10,000 and ISO8/Class 100,000, GMP facilities and the validation process (including Design Qualification (DQ), Installation Qualification (IQ), Operational Installation (OQ) and Product Qualification (PQ).