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.
Preclinical safety studies
per year
Clinical trials
per year
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:
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.
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
The Year in Review 2023
Never Miss an Issue of The Altascientist—Subscribe!
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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.
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.
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
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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!
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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.
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.
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.
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