How Is Partnering with Altasciences for Your First-in-Human Clinical Trials Different?

Advancing your molecule to first-in-human (FIH) clinical trials is a major milestone in your drug development program. Altasciences is here to help you get there, conduct your study, and provide you with a full range of complementary services.  

A Different Kind of CRO

Altasciences offers a unique integrated approach that can reduce program timelines by as much as 40%, lowering costs and getting better drugs to the people who need them, faster.

  • Regulatory expertise
    o  
    Our regulatory advisors have extensive experience navigating complex regulatory processes, ensuring your IND and CTA applications are submitted and processed swiftly and efficiently.
  • Scientific and operational expertise
    o   You can trust our team to deliver high-quality, customized solutions for your clinical trial needs.   
  • Pharmaceutical manufacturing
    o   We offer a wide range of manufacturing services to support your preclinical and clinical trials.
  • Bioanalysis
    o   With over 200 highly trained specialists and a capacity of over 60K study samples per month, Altasciences has the capacity to process your data quickly.
  • Project management

A single, dedicated project manager, along with a proprietary information-sharing database, means you only have to Tell Us OnceTM. Learn more about Altasciences’ FIH solutions.

Speak with one of our experts.

Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining 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.