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Enzyme Screening Kits – selectAZyme™
Enzyme Screening Kits – selectAZyme™
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Biocatalytic Oligonucleotide Synthesis Technology
Synthesis of single stranded RNA oligonucleotides
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Enzyme panels available to support Oligonucleotide synthesis
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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 Catalog Peptides for Research Use
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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 digitizes conventional on-site client tours and audits.
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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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Delivering comprehensive solutions to support drug substance (API) and drug product development programs.
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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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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
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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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A global distribution solution to safeguard your patients and clinical trials
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An intuitive and logical way to manage the key components of clinical trials
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From Kick-Off to Go-Live in 2 Weeks
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Add these products and services to your IRT build to increase its efficiency, compliance, and transparency.
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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 serialization
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Pediatric solutions from development to commercialization
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Supporting clients in developing their serialization 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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Dr Stewart McWilliams – VP Quality and Regulatory Affairs
Dr Stewart McWilliams – VP Quality and Regulatory Affairs
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