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Ireland Life Science Hub · Verified CDMO Directory

Ireland CDMO Directory & Sourcing Engine 2026

Search every major Contract Development and Manufacturing Organization (CDMO) operating in Ireland. Compare facility capabilities, containment ratings (OEB 4/5), spray drying platforms, biologics capacity, and regulatory licenses.

15 Verified Irish CDMO Facilities
#3 Global Pharma Exporter
€100B+ Annual Life Science Exports
Dual FDA & EMA Compliant Sites
Capabilities:
Aenova Group (Temmler Ireland) logo
Aenova Group (Temmler Ireland)
Killorglin, Co. Kerry
Modified Release Pellets & Spray Drying

Aenova Competence Center for spray drying and modified release pellets, trading on-site as Temmler Ireland Ltd. Over 50 years of site experience (since 1972) producing oral solids and inhalation powders.

Aenova Group Competence Center for modified release pellets
Employees
~70
Potency Rating
OEB 4
Capabilities
Oral Solid Dose Spray Drying Modified Release Pellets Inhalation Powders Granulation & Coating
Certifications
EMA (EU GMP) PMDA (Japan) ISO Certified MFDS
Almac Group Craigavon logo
Almac Group Craigavon
Craigavon, Co. Armagh
Peptide Synthesis & Commercial Drug Product

Opened a £65M, 100,000 sq ft commercial manufacturing facility in March 2025 for oral dose and potent drug products, alongside a separate 28,000 sq ft GMP peptide API synthesis plant (completed 2024) supporting growing demand for peptide therapeutics.

£65M commercial facility (2025) plus 28,000 sq ft peptide synthesis plant (2024)
Employees
Thousands of staff (NI's largest indigenous life sciences employer)
Potency Rating
cGMP Multi-suite
Capabilities
Peptide API Manufacturing Commercial Drug Product Clinical Trial Supply Sachet Formulation Drug Discovery
Certifications
FDA Approved EMA (EU GMP) MHRA ISO 9001
APC (Applied Process Company) logo
APC (Applied Process Company)
Loughlinstown, Co. Dublin
Pharmaceutical Process Development (Synthetics & Biologics)

APC (Applied Process Company) is a Dublin-based pharmaceutical process development organization, spun out of UCD in 2011 by Dr. Mark Barrett and Prof. Brian Glennon. It focuses on process development and scale-up rather than commercial manufacturing itself — GMP manufacturing is handled by sister company VLE Therapeutics as part of their joint 'Medicine Accelerator' campus. A €100M expansion announced in 2024 is adding 300 R&D jobs and a new 130,000 sq ft building.

€100M 'Medicine Accelerator' campus expansion (2024) — largest biopharma R&D build in Ireland
Employees
Several hundred, growing toward 600+
Potency Rating
Process Development (GMP via sister co. VLE Therapeutics)
Capabilities
Process Development Chemistry & Crystallization Engineering Tech Transfer HPAPI Development Upstream/Downstream Bioprocessing Cell & Gene Therapy Tech Transfer
Certifications
Bimeda logo
Bimeda
Tallaght, Co. Dublin
Veterinary Contract & Toll Manufacturing (Liquids)

Founded in Ireland in 1960, Bimeda is a global animal health company whose Tallaght, Dublin facility offers contract and toll manufacturing plus private-label production for distributors and international companies in liquid veterinary dosage forms — oral drenches, nutritional liquids, ectoparasiticides and disinfectants — alongside its own branded veterinary product lines.

Explicit contract & toll manufacturing plus private-label production for outside companies
Employees
Part of 1,000+ employee global group
Potency Rating
Liquid Veterinary Dosage Forms
Capabilities
Contract & Toll Manufacturing Private Label Manufacturing Oral Drenches Nutritional Liquids & Supplements Ectoparasiticides Disinfectants
Certifications
HPRA-Regulated EU GMP
Cambrex (Q1 Scientific) logo
Cambrex (Q1 Scientific)
Waterford, Co. Waterford
cGMP Stability Storage & Testing

Acquired by Cambrex in 2022, this facility features 40+ walk-in ICH stability storage chambers and cryogenic freezers down to -80°C.

40+ walk-in cGMP stability chambers (-80°C to +50°C range)
Employees
Specialist stability storage team
Potency Rating
-80°C Cryogenic to +50°C
Capabilities
Stability Storage ICH Conditions Cryogenic Storage cGMP Warehousing Biologic Stability
Certifications
HPRA Licensed EU GMP FDA Registered ICH Q1A(R2)
Chanelle Pharma logo
Chanelle Pharma
Loughrea, Co. Galway
Generic Human & Veterinary Pharmaceuticals + Contract Manufacturing

Ireland's largest indigenous manufacturer of generic pharmaceuticals for both human and veterinary use. Founded in 1985 by Michael H. Burke in Loughrea, Co. Galway, the company grew over almost four decades into a group holding 1,200+ human and 3,000+ animal health licenses, the largest veterinary licence portfolio of any animal health company in the EU, exporting to 90-100 countries worldwide. Operations run across two divisions: Human Health, manufacturing generic prescription and OTC medicines, and Animal Health, established in the UK market since 1991 with 50+ active brands across trade, veterinary and pet retail channels. The Loughrea campus itself has grown with the business, with a 2021 conversion adding a further 35,000 sq ft manufacturing facility at Ballinasloe, alongside the original site's multiple production buildings and R&D laboratories. Beyond its own generics portfolio, Chanelle offers contract development, manufacturing and packaging services to other human and animal health companies, backed by HPRA licensing and an FDA-approved manufacturing line (Spot On, operational since September 2019). In February 2024, founder Michael H. Burke sold the company to UK private equity firm Exponent for an estimated €300 million and retired. Angelo Gatto was appointed CEO that August, bringing 25 years of pharmaceutical leadership experience from Johnson & Johnson, Pfizer, Aenova Group and Adragos Pharma to lead the next phase of growth.

Ireland's largest indigenous generics manufacturer, with 1,200+ human & 3,000+ animal health licenses
Employees
Approximately 550
Potency Rating
cGMP Human & Veterinary Manufacturing
Capabilities
Generic Drug Manufacturing Contract Manufacturing & Packaging Human Health Animal Health Product Development Regulatory Strategy Advisory
Certifications
HPRA Licensed FDA-Approved Facility (Spot On line, 2019)
EirGen Pharma logo
EirGen Pharma
Waterford, Co. Waterford
High-Potency OSD & Oncology

Specializes in high-potency oral solid dose medicines for oncology and rare diseases. Produces 520M dosage units annually across 60 countries, targeting 1B units/yr by 2027.

High-containment oncology leader (Targeting 1B units/yr by 2027)
Employees
160+
Potency Rating
OEB 4 (High Containment)
Capabilities
High-Potency OSD Oncology Softgel Capsules Rare Diseases Film-Coated Tablets
Certifications
FDA Approved EMA (EU GMP) HPRA Licensed ISO Certified
HiTech Health logo
HiTech Health
Ballynahown, Co. Galway
Cell & Gene Therapy (ATMP)

First Irish CDMO licensed by HPRA for cell and gene therapy (ATMP) manufacturing, confirmed by independent press coverage (Irish Times, Feb 2024). Provides drug substance, drug product formulation, and cryogenic cold-chain logistics.

Ireland's first HPRA-licensed ATMP cell & gene therapy CDMO
Employees
20-50
Potency Rating
GMP-Classified Aseptic Cleanrooms
Capabilities
Cell Therapy Gene Therapy ATMP Sterile Injectables Cold Chain Logistics
Certifications
HPRA Licensed EMA (EU GMP) FDA Registered
Hovione Cork logo
Hovione Cork
Ringaskiddy, Co. Cork
API Synthesis & Spray Drying

Hovione describes itself as a global leader in spray drying and particle engineering for inhalable therapies and low bioavailability oral drugs. Operates 24/7 continuous production with GEA and Büchi platforms on the former Pfizer Lipitor API site, acquired in 2008/2009.

Nearly doubled spray-drying capacity in a 2024 multi-million-euro expansion
Employees
300+
Potency Rating
Highly Potent API Capable
Capabilities
API Manufacturing Spray Drying Inhalation Particle Engineering Amorphous Solid Dispersion
Certifications
FDA-Inspected EU GMP (HPRA-Inspected) ICH Compliant
PCI Pharma Services Meath logo
PCI Pharma Services Meath
Stamullen, Co. Meath
Injectable Packaging & Autoinjectors

Existing 45,000 sq ft site paired with new 82,000 sq ft facility dedicated to final assembly, labeling, and packaging of biologic injectables, pre-filled syringes, and autoinjectors.

127,000 sq ft biologics & autoinjector packaging hub
Employees
250+
Potency Rating
Biologics Packaging
Capabilities
Injectable Packaging Autoinjectors Pre-filled Syringes Vial Fill & Finish LEED Gold Facility
Certifications
FDA Registered EMA (EU GMP) HPRA Licensed LEED Gold Target
Pinewood Healthcare logo
Pinewood Healthcare
Clonmel, Co. Tipperary
Oral Liquids/Suspensions, Powders & Creams — Generic Licensing & Contract Manufacturing

Founded in 1976 by Michael Costello to serve Ireland's renal/dialysis care market, Pinewood Healthcare has been owned by India's Wockhardt Group since a 2006 acquisition (~$150M). Manufactures oral liquids, suspensions, powders, creams and ointments — both its own generic portfolio (200+ licensed formulations across 30+ countries) and third-party contract manufacturing.

Ireland's renal/dialysis-care pioneer, Wockhardt-owned since 2006
Employees
300-400 (across Tipperary manufacturing & Dublin distribution)
Potency Rating
cGMP Oral Liquids, Powders & Semi-Solids
Capabilities
Contract Manufacturing Generic Licensing Oral Liquids & Suspensions Non-Penicillin Powders Creams & Ointments White Label Manufacturing
Certifications
HPRA GMP Licensed HPRA GDP Licensed ISO 9001 ISO 13485
Sterling Pharma Solutions logo
Sterling Pharma Solutions
Ringaskiddy, Co. Cork
API Development & Manufacturing, Peptides, Large-Scale Chromatography

Acquired from Novartis in 2022, this 111-acre Ringaskiddy campus (operating since 1994) is one of Sterling Pharma Solutions' largest global API manufacturing sites, led by EVP & Site Head Maeve Byrne. Specializes in peptide manufacturing and large-scale chromatography alongside general API development and manufacturing.

111-acre ex-Novartis API campus — 30+ reactor trains, 175m³ total vessel capacity
Employees
350+
Potency Rating
175m³ vessel capacity, 250L-10,000L batch sizes
Capabilities
API Manufacturing Peptide Manufacturing Large-Scale Chromatography High Potency APIs Hazardous Chemistry Tech Transfer & Scale-Up
Certifications
HPRA Licensed ANVISA HSA (Singapore)
Thermo Fisher Scientific (Patheon) logo
Thermo Fisher Scientific (Patheon)
Ringaskiddy, Co. Cork
API Drug Substance & Process Chemistry

Acquired from GSK in 2019 for €90M, this manufacturing site traces its roots to 1975 and doubled its lab and analytical capacity in a 2023 expansion, serving complex small-molecule API manufacturing for global pharmaceutical customers.

Doubled lab & analytical capacity in a 2023 expansion
Employees
500+
Potency Rating
cGMP API Manufacturing
Capabilities
API Drug Substance Process Chemistry Analytical Development Commercial API Supply
Certifications
FDA-Inspected EU GMP ICH Q10
TopChem Pharmaceuticals logo
TopChem Pharmaceuticals
Ballymote, Co. Sligo
Niche & Low-Volume Active Pharmaceutical Ingredients (APIs)

Founded in 2006, TopChem is a GMP manufacturer of niche, low-volume active pharmaceutical ingredients and excipients that are difficult for customers to source elsewhere. A new Collooney, Co. Sligo facility came online in 2024, roughly tripling total production capacity with a dedicated new R&D centre. Sole API supplier for the only FDA-approved Bretylium Tosylate injection on the US market.

2024 Collooney facility expansion tripled production capacity
Employees
Low-to-mid 20s (specialist team)
Potency Rating
Niche/Low-Volume API Manufacturing
Capabilities
Commercial API Manufacturing Custom Chemical Synthesis API Product Development Reference Standards & Impurities Purification Process Upgrades
Certifications
EU cGMP Certified FDA Inspected
WuXi Biologics Dundalk logo
WuXi Biologics Dundalk
Dundalk, Co. Louth
Biologics Drug Substance & Drug Product

Ireland's first WuXi Biologics manufacturing site (announced 2018, €325M initial investment), featuring 48,000L fed-batch bioreactor capacity using single-use and continuous bioprocessing technology. Distinct from the adjacent WuXi Vaccines facility on the same campus, which was sold to Merck/MSD in 2025 — this biologics drug substance/drug product plant remains WuXi-operated and gained EMA commercial manufacturing approval in August 2025.

ISPE Facility of the Year 2023 — 48,000L single-use biomanufacturing plant
Employees
600+ (2024 campus figure)
Potency Rating
Biologics Single-Use
Capabilities
Biologics Manufacturing Single-Use Bioreactors Monoclonal Antibodies Recombinant Proteins Continuous Bioprocessing
Certifications
HPRA Licensed EMA (EU GMP) — commercial approval Aug 2025

At a Glance Comparison — Ireland CDMO Sites

Quick reference matrix of top contract development and manufacturing facilities operating in Ireland. Click any site to submit an inquiry.

Company / Site Location Primary Focus Containment / Scale Regulatory Approvals Action
Aenova Group (Temmler Ireland) Killorglin, Co. Kerry Modified Release Pellets & Spray Drying OEB 4 EMA (EU GMP), PMDA (Japan), ISO Certified Inquire →
Almac Group Craigavon Craigavon, Co. Armagh Peptide Synthesis & Commercial Drug Product cGMP Multi-suite FDA Approved, EMA (EU GMP), MHRA Inquire →
APC (Applied Process Company) Loughlinstown, Co. Dublin Pharmaceutical Process Development (Synthetics & Biologics) Process Development (GMP via sister co. VLE Therapeutics) Inquire →
Bimeda Tallaght, Co. Dublin Veterinary Contract & Toll Manufacturing (Liquids) Liquid Veterinary Dosage Forms HPRA-Regulated, EU GMP Inquire →
Cambrex (Q1 Scientific) Waterford, Co. Waterford cGMP Stability Storage & Testing -80°C Cryogenic to +50°C HPRA Licensed, EU GMP, FDA Registered Inquire →
Chanelle Pharma Loughrea, Co. Galway Generic Human & Veterinary Pharmaceuticals + Contract Manufacturing cGMP Human & Veterinary Manufacturing HPRA Licensed, FDA-Approved Facility (Spot On line, 2019) Inquire →
EirGen Pharma Waterford, Co. Waterford High-Potency OSD & Oncology OEB 4 (High Containment) FDA Approved, EMA (EU GMP), HPRA Licensed Inquire →
HiTech Health Ballynahown, Co. Galway Cell & Gene Therapy (ATMP) GMP-Classified Aseptic Cleanrooms HPRA Licensed, EMA (EU GMP), FDA Registered Inquire →
Hovione Cork Ringaskiddy, Co. Cork API Synthesis & Spray Drying Highly Potent API Capable FDA-Inspected, EU GMP (HPRA-Inspected), ICH Compliant Inquire →
PCI Pharma Services Meath Stamullen, Co. Meath Injectable Packaging & Autoinjectors Biologics Packaging FDA Registered, EMA (EU GMP), HPRA Licensed Inquire →
Pinewood Healthcare Clonmel, Co. Tipperary Oral Liquids/Suspensions, Powders & Creams — Generic Licensing & Contract Manufacturing cGMP Oral Liquids, Powders & Semi-Solids HPRA GMP Licensed, HPRA GDP Licensed, ISO 9001 Inquire →
Sterling Pharma Solutions Ringaskiddy, Co. Cork API Development & Manufacturing, Peptides, Large-Scale Chromatography 175m³ vessel capacity, 250L-10,000L batch sizes HPRA Licensed, ANVISA, HSA (Singapore) Inquire →
Thermo Fisher Scientific (Patheon) Ringaskiddy, Co. Cork API Drug Substance & Process Chemistry cGMP API Manufacturing FDA-Inspected, EU GMP, ICH Q10 Inquire →
TopChem Pharmaceuticals Ballymote, Co. Sligo Niche & Low-Volume Active Pharmaceutical Ingredients (APIs) Niche/Low-Volume API Manufacturing EU cGMP Certified, FDA Inspected Inquire →
WuXi Biologics Dundalk Dundalk, Co. Louth Biologics Drug Substance & Drug Product Biologics Single-Use HPRA Licensed, EMA (EU GMP) — commercial approval Aug 2025 Inquire →

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