Almac Sciences Limited

Craigavon, United KingdomFEI 3008699637API manufacture registered

Almac Sciences Limited is a drug establishment in Craigavon, United Kingdom, registered with the US FDA under FEI 3008699637. Its registered operations are: Analytical testing, API manufacture. 8 EU/UK GMP certificates are matched to this site, 4 inspected within the last three years.

Sources: FDA Drug Establishments Current Registration Site (checked 2 Nov 2026); EudraGMDP; MHRA GMDP. Methodology

Registered operations

Business operations this establishment declares in its FDA registration. Registration is not an approval and says nothing about EU or UK GMP status.

Analytical testingAPI manufacture

GMP documents matched to this site (9)

DocumentAuthorityInspectionSource
UK GMP 31890 Insp GMP/IMP 31890/16997281-0010 [V]
GMP certificate
MHRA7 May 2025
within 3-year review window
MHRA-GMDP
UK API 31890 Insp GMP 31890/383321-0022
GMP certificate
MHRA7 May 2025
within 3-year review window
MHRA-GMDP
UK GMP 31890 Insp GMP/IMP 31890/16997281-0010 [H]
GMP certificate
MHRA7 May 2025
within 3-year review window
MHRA-GMDP
UK MIA(IMP) 31890 Insp IMP 31890/16997281-0005[I]
GMP certificate
MHRA6 Feb 2025
within 3-year review window
MHRA-GMDP
UK API 31890 Insp GMP/GDP 31890/383321-0015 [V]
GMP certificate
MHRA16 Dec 2019
outside 3-year review window
MHRA-GMDP
UK API 31890 Insp GMP 31890/383321-0016
GMP certificate
MHRA16 Dec 2019
outside 3-year review window
MHRA-GMDP
UK API 31890 Insp GMP/GDP 31890/383321-0015 [H]
GMP certificate
MHRA16 Dec 2019
outside 3-year review window
MHRA-GMDP
UK API 31890 Insp GMP 31890/383321-0001
GMP certificate
MHRA21 May 2009
outside 3-year review window
MHRA-GMDP
UK API 31890
API registration
MHRA—MHRA-GMDP

A GMP document is matched to this site when its address names the site's street and its city or postcode. In our latest internal review 59 of 60 sampled matches were the right site (not yet independently reviewed; measured match quality). Check the certificate's own address before relying on it. The three-year review window is the EMA guideline default after an inspection, not an official expiry date.

What this page does not show

  • Which substances are made here: DMFs and CEPs are filed by organisations, not sites, so we do not link substances to this site.
  • Capacity, scale, price or current availability: no regulator publishes these.
  • FDA inspection classifications for this site, which are not yet linked.