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A Fast and Reliable Turnkey Solution
Whether springboarding your first-in-human study, generating data that informs your global registration trials, completing required Phase I studies for your NDA submission or post-marketing commitment fulfillment, Altasciences is poised and ready to accelerate your clinical pharmacology needs with our turnkey solutions.
With a deep understanding of the challenges and nuances in drug development, Altasciences is committed to providing solutions that safely accelerate timelines, improve outcomes, and ensure regulatory compliance. Discover the difference through the insightful resources below.
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Find out how open dialogue, aligned expectations, and direct communication with the sponsor contributed to a clinical trial start-up of only 3.5 weeks.
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Discover how Altasciences' unique site-selection process ensures a strong feasibility plan and rapid study initiation.
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Explore the important role of drug interaction studies in minimizing adverse effects and optimizing treatment response.
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Learn how the FDA has undertaken efforts to manage the misuse and abuse of prescription drugs, including opioid analgesics, through guidelines for understanding the abuse potential of new drugs.
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Discover how ethnobridging studies streamline the approval process in Asian markets and address potential disparities in drug metabolism between Asian and non-Asian populations.
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