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Providing services for all stages of drug development for small (including highly potent) molecules and peptides.
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API Development and Manufacture – Late Phase
Highly Potent API Manufacture
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Extensive experience in QC and Analytical Support
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Enzyme Screening Kits – selectAZyme™
Enzyme Screening Kits – selectAZyme™
Biotransformation Process Development
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Biocatalytic Oligonucleotide Synthesis Technology
Synthesis of single stranded RNA oligonucleotides
Synthesis of double stranded oligonucleotides
Enzyme panels available to support Oligonucleotide synthesis
Peptide and Protein Technology
A range of peptide & protein services from early phase to commercial launch
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Custom Peptide Synthesis for Research Use
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Specialist Catalogue Peptides for Research Use
Specialist Catalogue Peptides for Research Use
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Site-specifically biotin labelled Chemokines
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GMP Peptide Manufacture
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Comprehensive range of Chemokine and Histone products with worldwide shipping and online discounts available.
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Fine chemical manufacture for pharmaceutical & health care, flavour/ fragrance and more
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Almac’s continuous flow technology platform enables access to better synthetic strategies
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Almac Sciences’ innovative virtual tour solution digitises conventional on-site client tours and audits.
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Expert development & manufacturing solutions for all phases of clinical trials
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Providing a range of solid oral dose development and manufacturing services from 3 state-of-the-art facilities
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Oral dose formulations to support your early phase clinical trials.
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Developing robust formulations and manufacturing processes suitable for late phase clinical trials.
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Flexibility, cost and time are key criteria in evaluating options in a ‘build or buy’ decision for your technology.
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Providing flexible tailored solutions
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Delivering comprehensive solutions to support drug substance (API) and drug product development programs.
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Pharmaceutical Method Development and Validation
Developing and validating over 300 drug substances and drug product methods each year
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Expertise in Release Testing including API, drug product, medical devices and biologics
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Comprehensive and cost-effective stability testing, study management and stability storage
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Skilfully guiding you to make the right decisions at the right time
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State-of-the-art laboratories with a comprehensive range of fully GMP spectroscopic equipment.
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Comprehensive and flexible Biological Testing solutions
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All our analytical laboratories are fully certified by the appropriate authorities (FDA, MHRA, INAB, HPRA).
Global Analytical Laboratory Testing Facilities
All our analytical laboratories are fully certified by the appropriate authorities (FDA, MHRA, INAB, HPRA).
Analytical Laboratory Facilities in the US
State-of-the-art US based labs support drug substance (API) and drug product (finished product) analytics across all phases of clinical development and into commercial release.
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The most comprehensive Global Clinical Supply Chain Solution in the marketplace
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Navigating the complexities of the clinical supply chain
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Global blinding experience across a range of investigational medicinal products.
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Efficient, flexible and innovative global packaging solutions
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Extensive global secondary clinical packaging solutions
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Changes to your clinical supply landscape require a quicker response and greater flexibility
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A global distribution solution to safeguard your patients and clinical trials
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Expert Qualified Persons (QPs) and an experienced support team for your trial
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Unlock new efficiencies through industry-leading technology
Clinical Technologies
Unlock new efficiencies through industry-leading technology
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An intuitive and logical way to manage the key components of clinical trials
IRT Startup Modes
From Kick-Off to Go-Live in 2 Weeks
IRT Boosters
Add these products and services to your IRT build to increase its efficiency, compliance, and transparency.
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ART™ – Drug Accountability & Reconciliation Tracking
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Access to industry-leading experts and clinical data integrations at your fingertips
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Helping you successfully launch your orphan drug products in to the EU market
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Over 50 years’ experience manufacturing solid oral dosage forms.
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From initial artwork and pack design, to commercial packaging and serialisation
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CBE – 30 Filing
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Paediatric solutions from development to commercialisation
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Supporting clients in developing their serialisation strategies to GS1 standards
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A range of storage conditions and flexible distribution solutions to meet your needs
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Flexibility, cost and time are key criteria in evaluating options in a ‘build or buy’ decision for your technology.
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