Almac House, 20 Seagoe Industrial Estate
Armagh, BT63 5QD
United Kingdom
Company Description
The Almac Group is an established contract development and manufacturing organization providing an extensive range of integrated services across the drug development lifecycle to the pharmaceutical and biotech sectors globally. Our innovative services range from R&D, biomarker discovery development and commercialization, API manufacture, pharmaceutical development, clinical trial supply, IRT (IVRS/IWRS) through to commercial-scale manufacture and specialized commercial packaging. The international company is a privately owned organization that has grown organically over the past five decades now employing over 5,600 highly skilled personnel across 18 facilities including UK, Europe, the US and Asia.
We have a global reputation for excellence built over 50 years of client service, delivering expertise right across the drug development lifecycle and offering a tailored solution to each of our clients.
Service Highlights:
API Services & Chemical Development
Providing integrated services from development to commercial scale of advanced intermediates and Active Pharmaceutical Ingredients (API), we offer a wide range of services for small molecules (including highly potent) and peptides. We have a proven track record of saving time and costs through the integration of our services and application of innovative biocatalysis and technology solutions:
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API development and manufacture
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Peptide & Protein Technologies
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Analytical Services
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Solid state services
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14C-radiolabeling
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Biocatalysis solutions
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Continuous flow chemistry
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Non GMP starting materials / intermediates
Pharmaceutical Development
Addressing the increasing pressure to bring clinical candidates through pipelines faster and with greater efficiency, we provide expert solid, oral dose pharmaceutical drug product development solutions. From developing a fit-for-purpose formulation for First-in-Human trials, to scaling up for late phase trials and ultimately commercialization, our solid oral dose, pharmaceutical development solutions are customized to meet our client needs.
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Pre-formulation
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Non-GMP development
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Early stage development
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Scale-up and later stage development
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Clinical trial manufacture
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High potency processing
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Analytical support
Commercial Services
Meeting all your commercial needs, we provide a wide range of customized commercial services from supporting your Orphan Drug / Gene Therapy product launch, commercial drug product manufacturing and/or specialized packaging of your drug product, to securing your supply chain with global serialization solutions.
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Commercial Product Launch & 3PL Distribution
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Solid Oral Dose Commercial Manufacturing
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Solid Oral Dose Commercial Packaging (Sachets, Stickpacks, Bottles, Blisters, Wallets)
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Specialized Commercial Packaging (Vial/Syringe Labelling, Complex Kit Assembly, Ultra Low Temperature Packaging)
Why work with Almac?
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50 years’ experience serving > 600 clients, high level of repeat business
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Financial stability and long term focus
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Focus on service integration to mitigate risk, reduce time and cost to market
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Quality driven and client focused
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Prepared to invest in new solutions to meet customers’ needs
Contract Service Categories
Contract Services Directory
Accelerated Stability Studies |
Analytical Laboratory Services |
Analytical Methods Development |
Analytical Validation Studies |
Anti-Counterfeiting Technology |
Assay Development |
Bioanalytical Analysis LC/MS/MS |
Bioanalytical Services |
Biocatalysis |
Bioprocessing |
Biostatistics |
Blending |
Calibration |
cGMP Synthesis |
Chemistry, Medicinal |
Chiral Separations, R&D |
Chromatographic Analysis, LC/GC |
Clinical Analysis |
Clinical Supply Management |
Clinical Trials Management |
Clinical Trials, Phase I |
Clinical Trials, Phase II |
Clinical Trials, Phase III |
Clinical Trials, Phase IV |
CMC (Chemistry, Manfacturing & Controls) |
Commercial Drug Sourcing |
Comparator Drug Purchasing |
Consulting, Quality Management Systems |
Consulting, Regulatory |
Contaminant Analysis |
Contract Development and Manufacturing Organization (CDMO) |
Contract Manufacturing |
Contract Packaging |
Custom Synthesis |
Dissolution Testing |
Distribution, Clinical Trials |
Distribution, Commercial |
Dosage Form Development |
Drug Development Services |
Efficacy Testing |
Encapsulation |
Environmental Analysis |
Environmental Monitoring |
European QP |
Extractables / Leachables Testing |
Fermentation |
Fluid Bed Processing |
Formulation Development |
HPLC |
Immunotoxicity Testing |
In Vitro Testing |
In Vivo Testing |
Manufacturing, API |
Manufacturing, API, High Potency |
Manufacturing, Capsules |
Manufacturing, Clinical Trials Supply |
Manufacturing, Controlled Substances |
Manufacturing, Custom |
Manufacturing, Dose Form, Non-Sterile |
Manufacturing, High Containment Operations |
Manufacturing, Oral Drug Delivery |
Manufacturing, Peptides |
Manufacturing, Powders, Non-Sterile |
Manufacturing, Proteins |
Manufacturing, Solid Dosage |
Manufacturing, Sustained Release |
Manufacturing, Tablets |
Mass Spectrometry |
Materials Analysis |
Medicinal Chemistry |
Metabolic Analysis |
Methods Development |
Methods Validation |
Micro FT-IR Analysis |
Microbiological Testing |
Micronization |
Organic Synthesis |
Packaging, Anti-Counterfeiting |
Packaging, Blister |
Packaging, Blister, Cold Form |
Packaging, Capsules |
Packaging, Clinical Trial Materials |
Packaging, Clinical Trials |
Packaging, Compliance |
Packaging, Design & Testing |
Packaging, Development |
Packaging, Electronic Pedigree |
Packaging, Injectables |
Packaging, Labels |
Packaging, Parenterals |
Packaging, Pouches |
Packaging, Powders |
Packaging, Solid Dosage |
Packaging, Unit Dosage |
Particle Characterization |
Particle Size Analysis |
Pharmacokinetics |
Pharmacovigilance |
Physical Testing |
Preclinical Testing Formulations |
Preformulation |
Process Analytical Technology (PAT) |
Process Characterization |
Process Development/Scale-Up Services |
Process R&D |
Process Validation Studies |
Project Management |
Protein Extraction/Purification |
Protein Synthesis |
Purification |
QA/QC |
Quality Control Testing |
Radiopharmaceuticals |
Raw Materials Analysis |
Regulatory Affairs Consultants |
Scale-Up |
Serialization |
Software |
Spray Drying |
Stability Studies |
Stability, ICH |
Statistical Analysis |
Storage |
Supply Chain Auditing |
Supply Chain Management |
Technology Transfer |
Third Party Logistics (3PL) |
Trace Metal Analysis, ICP |
UV-VIS Spectrophotometer Analysis |
Validation, Manufacturing |
Water Testing: Chemical |
Water Testing: Microbiology |
X-Ray Fluorescence |
X-Ray Powder Diffraction |
X-Ray Spectroscopy |