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.
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
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.