Outsourcing Drug Development

  • Outsourcing Drug Development
  • Regulatory processes can be challenging, and potential solutions can be found in broadening your focus to include clinical sites in the U.S. and Canada for your drug development strategy. With an understanding of how regulatory agencies and market environments may differ, you will be in a better position to optimize your program. In Altasciences’ on-demand webinar, A Hop Across the Pond, Ingrid Holmes, Vice President of Global Clinical Operations, and Dr.

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    The drug development landscape has been evolving over the years, from an earlier emphasis on blockbuster drugs developed in-house by large pharmaceutical companies, t

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    We are often asked about the advantages of working with an integrated CRO/CDMO.

    In 2021, you did incredible things — and we are grateful to have been part of your journey.

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    Your drug discovery phase is nearing completion and your funding is in place. What comes next?

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    Bringing new drugs to market, from lead candidate selection through preclinical testing, to clinical proof of concept, is a complex, time-consuming, and costly process.

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    Early-phase drug discovery and drug development are complex processes, where many moving parts can, and do, influence the success of a program.

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    In our February 2021 blog we discussed protocol design concepts for ethnobridging in Phase I clinical trials.

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    What Data Managers Do

    Gathering, analyzing, and presenting the data to support life-altering new medicines for people around the world is a long, complex, and detailed proces

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    Renowned for our full-service offering, we often get asked — how does Altasciences manage the development process for biologics and biosimilars so seamlessly from the require

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