Outsourcing STREAM

  1. How To Boost Disclosure Efficiencies With Outsourcing 11/1/2018

    In this webinar, you’ll hear about exciting new advisory and managed disclosure services from TrialScope, including: compliance, policy and process assessments, as well as plain-language summaries, protocol registration, results posting, and redaction services.

  2. Proactive Drug Development: Explained 1/30/2023

    Watch this short video to learn about Proactive Drug Development with Altasciences.

  3. Imagine… Easier, Proactive Drug Development 2/14/2023

    Imagine partnering with a single CRO/CDMO for your early phase drug development. With Altasciences, you don’t have to imagine—learn how they’re able to deliver for your project.

  4. Flipping The Drug Development Industry On Its Head 6/18/2024

    The video dives into the obstacles of the traditional outsourcing relationship between CROs and sponsors, and how Altasciences has broken from tradition to offer an alternative model.

  5. Streamlining Patient Access To Cell And Gene Therapies 12/21/2023

    Learn about the obstacles patients encounter when seeking CGTs and explore how technology and patient services can empower manufacturers and clinical teams to help patients overcome barriers.

  6. Navigating The Unique Attributes Of Psychedelic Drug Development 1/22/2024

    Join our panel of experts for an in-depth review of the FDA's guidance on psychedelic drug development, exploring necessary methodological adaptations for safety, pharmacology, and efficacy.

  7. Big Impact With A Personal Touch 1/30/2023

    Transforming lives. Improving human health. Bringing new therapies to life. Altasciences' CRO and CDMO services deliver.

  8. We Are Altasciences: Proactive Drug Development 1/30/2023

    When you partner with Altasciences, you get a single source outsourcing partner who knows your program from end to end and who can anticipate your needs, for a seamless and simplified experience.

  9. Altasciences Clinical Services At A Glance 1/30/2023

    We can support your entire drug development program end to end, or you can partner with us for just one element. We offer you complete flexibility.

  10. Improving Sponsor Oversight Of The Trial Master File 2/15/2023

    In the face of increasing documentation requirements and trial complexity, discover how global biopharmaceutical company Chiesi and its CRO partners collaborated to ensure ongoing oversight compliance.