Our Solutions

Fast and Reliable Data for Your First-in-Human Trials

 

Data gathered during first-in-human (FIH) trials is critical to making go/no-go decisions in drug development. At Altasciences, we provide you with: 

  • Timely sample analysis and scheduling flexibility
  • Rapid turnaround of PK/PD analysis between cohorts (within 48 to 72 hours)
  • Excellent communication and information sharing between clinic and lab  
  • Early proof-of-concept signals

Our focus on early phase research, our integrated preclinical, clinical, manufacturing, and laboratory operations ensure data is shared with full transparency. PK analysis is built into your program schedule from the start, and dosage adjustments can be accommodated for safe and quick
decision-making.

Partner with us to get quality data you can rely on, fast.

Contact us

You may also be interested in the following:

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.

Working as a flexible, attentive extension of your team, we offer comprehensive drug development services to move your molecule forward.

Sign up for exclusive content

Join our list of 10,000+ VIP members and have access to our exclusive content.

You can unsubscribe at any time. For more details, please review our privacy policy.

Stay connected