WELCOME TO ATHERION BIORESEARCH
A True Partner in Drug Development
We are a full-service or bespoke clinical research company enabling clients to develop their technology and grow their pipeline. Whether it be preclinical research from target or drug discovery to clinical research from First in Human to Phase IV, we are passionate about working with you to develop innovative medicines that will positively impact people's lives.
We provide high quality services to all of our clients and as we grow, our commitment to your needs remains the key driver behind our company. Our team of professionals is here to inspire you with their unique ideas and abilities - get in touch today to learn more.
We are a clinical research organization (CRO) established by a team of experienced drug development professionals.
We are dedicated to helping our partners advance their pipelines.
We work relentlessly to provide assistance, insight, and solutions for pharmaceutical and biotechnology companies of all sizes. Get in touch to learn more.
Derisking Your Drug Development Pipeline
We understand the risks of using a CRO:
Lack of engagement
Constant changes of scope
Gaps in capabilities
We will work with you to provide a high value, reasonable cost solution to meet and exceed your drug development needs.
"Big results require big ambitions"
Expertise to Meet Your Needs
We have decades of experience in a wide variety of disease areas, in research and development, in diagnostics (including radiopharmaceuticals) and therapeutics, and in drug chemistry and manufacturing.
Broad Clinical Experience
1 / Radiopharmaceuticals
2 / Oncology and Immuno-oncology
3 / Rheumatology
4 / Cardiology
5 / Neurology
6 / Ophthalmology
7 / Respiratory
8 / Musculoskeletal
Services we can provide include, but are not limited to:
Preclinical study design
Clinical trial design
Preclinical and Clinical trial project management
Regulatory document preparation
GMP manufacturing and CMC oversight
Study design and oversight
Lead candidate, early efficacy, and safety study design and management
Clinical Trial Operations
Site selection, monitoring, and project management
Document preparation and submission
Clinical study reports and FDA/EMA submissions
Onsite trial monitoring