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    Providing services for all stages of drug development for small (including highly potent) molecules and peptides.
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      Integrated API manufacturing solutions throughout the drug development lifecycle.
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      Extensive experience in QC and Analytical Support
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      A range of peptide & protein services from early phase to commercial launch
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      Developing robust formulations and manufacturing processes suitable for late phase clinical trials.
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      All our analytical laboratories are fully certified by the appropriate authorities (FDA, MHRA, INAB, HPRA).
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        All our analytical laboratories are fully certified by the appropriate authorities (FDA, MHRA, INAB, HPRA).
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        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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    Unlock new efficiencies through industry-leading technology
    • Clinical Technologies
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      Unlock new efficiencies through industry-leading technology
    • Almac Trial Coordinator™
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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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      Access to industry-leading experts and clinical data integrations at your fingertips
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      Utilise Almac’s industry leading IRT – submit your IRT request for immediate review
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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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      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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