Locations
A global network of dedicated Pharma specialists.
Frederikssund / DK:
- Certified cGMP manufacturing plant
- DMA approved for the manufacture of sterile and aseptically filled intermediates in accordance with:
- EU GMP Part 1 – Basic Requirements for Medicinal Products
- Annex 1 - Manufacture of Sterile Medicinal Products
Leek / UK:
- MHRA approved for the manufacture of API to EU GMP (ICHQ7)
- FDA inspected for the manufacture of API to USA GMP
- KFDA inspected for the manufacture of API to Korea
- EXCiPACT GMP certified
- ISO 9001:2015 – Quality Management System
Alabaster / USA:
- FDA registered API manufacturer
- Compliance with manufacture of API to EU GMP (ICHQ7)
- US FDA inspected
Mill Hall / USA:
- EXCiPACT GMP certified
- ISO 9001:2015 – Quality Management System
Shiga / Japan:
- EXCiPACT GMP certified
- ISO 9001:2015 – Quality Management System
Quality
The pharmaceutical industry is highly regulated, and products of high and consistent quality are essential. When manufactured ingredients are used in drug or vaccines formulations, risk of quality failures must be minimised, and ultimately patient safety ensured.
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