About Altasciences

  • About Altasciences
  • Altasciences Has You Covered From Coast to Coast

    Accelerate your drug development timelines by up to 40% with an integrated CRO/CDMO by your side, from lead candidate selection to clinical proof of concept, and beyond.

    Our scientific and operational teams move in unison to provide a seamless and synchronized drug development roadmap with research activities running in parallel. With nine strategically placed research and manufacturing facilities across North America, Altasciences has the capacity to help you get better drugs to the people who need them, faster.

    700+ 
    Preclinical safety studies
    per year
    285+ 
    Clinical trials
    per year
    720,000+ 
    Study samples trials
    per year

    With multiple points of entry, Altasciences' integrated, full-service solutions help you make educated and more complete early phase drug development decisions. When you choose the right partner, you only need one.

    Get a glimpse of the unique expertise at each of our nine facilities: Altasciences Facilities

    You may also be interested in the following:

    •   Digital Brochure: Our Expertise at a Glance
    •   Video: Accelerate Your Data With Our Co-Located Clinic and Lab
    •   Webpage: Proactive Drug Development
    •   Video: Quick Chat With CEO Chris Perkin: One Operational Structure

     

    How Is Your CRO Handling Your Trial Data?

     

    Best Practices for a Successful, Multi-Step Data Journey

    In this issue of The Altascientist, we guide you through the complex, multi-step data journey for Phase I clinical trials, from study conceptualization and protocol development, to data collection and analysis, through to final regulatory submission. We highlight best practices and approaches to mitigate challenges, and show how integration and collaboration build the strongest datasets for your drug development program.

    Building your early phase clinical data, from protocol to regulatory submission.

     

    Speak with an expert to learn more about our service offering.

    Have a few more minutes? Check out these insightful resources:

    •   The Altascientist—CDISC Data Standards
    •   Fact Sheet—Comprehensive Research Support
    •   Blog—Data Management Excellence

    Altasciences' Truly Integrated Platform

    Never Miss an Issue of The Altascientist—Subscribe!

     
    Altasciences
     

    Listen to The Altascientist on the Go

    Did you know? The Altascientist: Scientific Journal is available as an audiobook series. Listen on our website or wherever you get your podcasts:


    Subscribe to Altasciences' podcast channel on your favorite streaming provider to never miss a new audiobook release.
      


     

    RECENT RELEASE 
    Audiobook: Nonclinical Studies in Cell and Gene Therapy: Key Considerations and Regulatory Guidance.ISSUE 36 — Nonclinical Studies in Cell and Gene Therapy: Key Considerations and Regulatory Guidance

    It is estimated that there are more than 6,000 monogenic diseases affecting over 350 million people worldwide. For these diseases, cell and gene therapy may provide a cure. 
    Listen now



    ABOUT THE ALTASCIENTIST
    A scientific journal written by our experts, The Altascientist is a deep dive into the critical processes behind early phase drug development. Available to read or to listen
     

    Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services.




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    OUR SERVICES
    Preclinical   —   Clinical   —   Manufacturing and Analytical
    Bioanalysis   —   Research Support
    Copyright © 2023, Altasciences, All rights reserved.


     

    Don’t Miss the Latest Altasciences News!

     

    Angel Reyes Joins Altasciences as General Manager of CDMO Services

    Altasciences is pleased to welcome Angel Reyes as General Manager, Contract Development and Manufacturing Organization (CDMO) Services. Having previously been the Director of Operations at Catalent, he brings to Altasciences over a decade of experience in management and supervisory roles.

    CONTINUE READING

     

    Altasciences Completes Expansion of New State-Of-The-Art Laboratory in Columbia, Missouri

    The impressive 8,000-square-foot space, which includes a test material department, features state-of-the-art equipment and forty-eight workbenches, with a vast range of services, including ligand binding assays, flow cytometry, biomarker analysis, and cell culture capabilities.

    CONTINUE READING

     

    IN OTHER NEWS…

    Altasciences’ Marie-Hélène Raigneau and Steve Mason Named Most Influential COOs in the Healthcare Industry to Follow in 2023

    In honor of this recognition, Insights Care published two in-depth interviews with Altasciences’ Co-chief Operating Officers, providing a glimpse into their daily roles, their journeys to becoming part of Altasciences, and their thoughts on the industry.

    •   Read Marie-Hélène’s interview

    •   Read Steve Mason’s interview

     

    View more Altasciences news on our website.

     

    It's Been a Minute, See What You Missed! Top 10 Life Science Resources


     

    Top 10 Life Science Resources 

    Your time is precious. Therefore, we’ve curated a selection of recently published expert insights, tips, case studies, and scientific and regulatory information, just for you. 

    Nonclinical Resources

    1. eBook: Safety Assessment for Ophthalmic Products

      Learn about the considerations and assessments necessary for performing nonclinical research on ophthalmic therapies, from species selection and routes of administration to preparing for first-in-human trials. Read it now.
       
    2. ​​The Altascientist: Issue No. 36 – Nonclinical Studies in Cell and Gene Therapy: Key Considerations and Regulatory Guidance

      Find out what the key factors are when developing nonclinical cell and gene therapies–including expert approaches to mitigating complex challenges, improving study efficiency, and maximizing translational opportunities to first-in-human (FIH) trials.​​​​​ Read or listen now.
    Clinical Services
    1. Video: Think Canada: The Team Behind Your Clinical Trials

      Learn about the inner workings of our clinical pharmacology unit in Montréal, and meet the dedicated team of experts driving the many trials conducted there, in this fun behind-the-scenes look. Watch the video.
       
    2. Podcast: FDA Guidance for Industry Psychedelic Drugs

      Listen to an in-depth discussion on the FDA’s recent draft guidance on clinical investigation of psychedelic drugs with Altasciences’ expert doctors, Denise Milovan, Debra Kelsh, and Beatrice Setnik. Listen to the podcast.
    Bioanalytical Services
    1. Fact Sheet: Bioanalytical Expertise for Immunomodulatory Drugs 

      See how Altasciences’ bioanalytical experts can provide support for your immunomodulatory drugs, and advance your drugs from preclinical to early phase clinical trials.​​​​​ Read the fact sheet.
       
    2. Blog: Choosing the Best Bioanalytical Platform for Your Program

      Explore how we determine the most appropriate and effective bioanalytical platform for your molecule. Read the blog.
      ​​​
    Manufacturing and Analytical Services
    1. The Altascientist: Issue No. 35 – Critical Considerations for the Safe and Compliant Manufacture of Highly Potent Drugs

      How the demand for manufacturing highly potent active pharmaceutical ingredients (HPAPIs) has increased, and the intricacies involved in manufacturing them safely. Read or listen now.
       
    2. Podcast: Successful Manufacturing of Clinical Trial Supply

      Uncover secrets from our formulation and pharmacy experts for effectively completing clinical trials, and resolving potential issues that could hinder your drug development timeline. Listen here.
    Research Support Services
    1. Educational Video: The Benefits of Conducting a Clinical Trial in Canada

      Gain valuable insights into Health Canada's Clinical Trial Application (CTA) submission and review process, along with answers to some of your most common questions. Watch it now.
       
    2. The Altascientist: Issue No. 34: Toxicokinetics, Pharmacokinetics, and Pharmacodynamics 

      Take a closer look at the collection and use of pharmacokinetic (PK) and pharmacodynamic (PD) data in early phase drug development, as well as the critical role of nonclinical toxicokinetic (TK) studies in guiding early phase clinical trials. Read or listen now.
    Visit Our Complete Resource Center

    Recent Regulatory Updates:

    Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services from lead candidate selection to clinical proof of concept, and beyond.


    Altasciences has been recognized as a 2023 CRO Leadership Award Champion in the Capabilities category, as voted by you in ISR’s annual CRO Quality Benchmarking survey.


    LET'S STAY CONNECTED!

    LinkedIn   

    YouTube   

    Blog

    OUR SERVICES
    Preclinical   —   Clinical   —   Manufacturing and Analytical
    Bioanalysis   —   Research Support
    Copyright © 2023, Altasciences, All rights reserved.

    Getting to the Heart of Science With Natasha Savoie

    Natasha Savoie, Senior Director of Quality Assurance at Altasciences, has an undeniable passion for science, a passion that drives her to ensure that the data we generate for our clients is reliable and precise.

    Watch this video to experience Natasha's unwavering dedication to science. 

    Hot off the Press!


     

    Altasciences Chosen by Virpax to Support the Development of a New Drug to Prevent Spread of Flu-like Viruses

    ​​​​​​Virpax Pharmaceuticals Inc. has chosen Altasciences to conduct preclinical studies in support of their new drug, an intranasal spray called AnQlar™. The drug is intended to prevent the spread of viruses such as influenza, COVID-19 and similar flu-like viruses. The studies were performed at Altasciences’ preclinical facilities located in Columbia, MO, and Scranton, PA, and are currently ongoing.
     

    Altasciences Completes Successful Phase I Trial of Ischemix’ Novel Compound for Treatment of Traumatic Brain Injury (TBI)

    ​​​​​​A Phase I trial of Ischemix, Inc.’s novel, proprietary cytoprotective drug candidate, CMX-2043, was successfully completed at Altasciences’ clinical facility in Montréal. The study was performed in a group of 80 healthy participants, to evaluate safety, tolerability, and pharmacokinetics of the drug. If successful, CMX-2043 could be a vital step to treating TBI, which is responsible for 60,000 deaths per year in the U.S.
     



    Let's Promote Your Project!

    Interested in a custom press release, written by our experts, to feature the great research we do together? Email us to get started!


    You may also be interested in:

    Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services.
     


    LET'S STAY CONNECTED!
     

    LinkedIn   

    YouTube   

    Blog

     

    OUR SERVICES
    Preclinical   —   Clinical   —   Manufacturing and Analytical
    Bioanalysis   —   Research Support
    Copyright © 2023, Altasciences, All rights reserved.

     

    Save Time. Choose the Right Regulatory Pathway.

     

    Advantages of Conducting Early Phase Clinical Research in Canada


    Given the regulatory constraints in Europe, Altasciences' Montréal facility continues to be an ideal choice for clinical research. Discover the benefits of conducting early phase research in Canada, such as time and cost savings.
     

    Advantages of Conducting Early Phase Clinical Research in Canada


    This issue of The Altascientist examines the advantages of conducting early phase clinical research in Canada, including 76 days in time savings, and a predictable regulatory review.​​​

    Download it Now!

     

    Determining the right regulatory pathway for your drug


    In this on-demand webinar, Leslie Dowling and Roland Jbeily walk you through different regulatory pathways available to safely get your drug to market as quickly as possible.

    Watch it Now!


    Altasciences’ Canadian clinical facility consists of seven Phase I units, at which we conduct over 100 trials every year. We support the full range of first-in-human studies, specialty studies, and therapeutic areas, such as ophthalmology, CNS, and substance abuse.

    We can help get you into the clinic faster—schedule a chat today!

     

    Take five minutes to explore these insightful resources:

    Podcast: The Benefits of Conducting a Clinical Trial in Canada 
    Drug Development Timelines: How Health Canada’s 30-Day Regulatory Review Process Could Provide an Advantage 
     

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