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.

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ABOUT US

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.

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Derisking Your Drug Development Pipeline

We understand the risks of using a CRO:

Lack of engagement
High costs
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"

Heraclitus

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

Services we can provide include, but are not limited to:

Preclinical study design
Clinical trial design
Preclinical and Clinical trial project management
Protocol writing
Monitoring
Regulatory consulting
Regulatory document preparation
GMP manufacturing and CMC oversight
Data interpretation
Manuscript writing