Clinical Trials Products and Services
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Site Management Organization
11/7/2023
Discover the power of clinical excellence with Acrostar's SMO Division, a dedicated entity operating as part of Novotech.
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Novotech Drug Development Consulting: Services For Success
6/27/2023
Delve into the details of this full-service global product development and strategic regulatory group that has a proven track record of successful FDA meetings and approvals.
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How ClinicReady Delivers Foundations For Success
8/8/2024
ClinicReady is the surrogate for outsourced drug development team for preclinical biotechs.
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One Step
6/20/2023
Make strides with a tailored, comprehensive suite of discovery and development services to rapidly progress your project and reduce time to market.
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FSP: Global Support To Fit Clinical Trial Management Needs
7/31/2025
Catalyst Flex provides flexible, scalable solutions and services to enhance our clients’ outsourcing needs. We are a specialized provider of multi-therapeutic functional solutions delivered by our experts.
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The North American Advantage
8/8/2024
With more than 80% of Avance Clinical’s biotech clients located in North America, the region has played a significant role in the almost three decades of the company’s growth.
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Integrated Trial Services
11/22/2024
We work as a single provider to empower patient and site participation in clinical trials. Our Integrated Trial Services team is dedicated to creating partnerships with our Sponsor and CRO clients, building strategic and unique combinations of solutions to accelerate trial timelines.
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Medical Writing For Clinical Trials
1/25/2024
For successful regulatory outcomes, we provide quality medical writing services for clinical trial documents, safety updates, and marketing applications.
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Navigate The Early Phases Of Product Development With Ease
6/16/2025
Early Phase Experts
As a full-service contract research organization, Southern Star Research has the knowledge, industry relationships and technical expertise to get your early-phase clinical trial up and running safely and efficiently.
With a broad range of experience delivering Phase 1 Healthy Volunteer, First in Human, First in Patient and Phase 2 trials, we know just how important it is for your asset to succeed in the early development lifecycle. Our experienced team will help you obtain high-quality data that will appeal to future investors, meet the requirements of international regulatory bodies such as the FDA, EMA, PMDA, and Health Canada, and prepare your product for larger Phase 3 and 4 studies, partnerships, licensing, and sale.
Whatever your clinical trial needs, we can provide a flexible, bespoke solution that will not only meet your regulatory requirements but also position your product for commercial success.
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Getting Biotechs GlobalReady
8/8/2024
Our proprietary GlobalReady model covers the entire drug development journey from robust EARLY PHASE clinical foundations with ClinicReady to seamless multi-regional Late phase expansion. All managed by the one award-winning CRO, saving time and costs and delivering rigorous globally accepted data.