Therapeutic Areas
20+ Years Experience Across Various Therapeutic Areas.
BioPharma Services has supported drug development programs across a broad range of therapeutic areas, dosage forms and product types.
Our experience is primarily focused on early-phase clinical trials and bioequivalence studies conducted in healthy volunteers. This allows sponsors to work with a clinical research team that understands the scientific, operational and regulatory considerations associated with diverse compounds, while maintaining a consistent approach to study execution, participant safety and data quality.
While most studies are conducted in healthy participants, BioPharma Services also has experience supporting select patient-based and rare-disease studies in collaboration with sponsors, investigators and therapeutic-area experts.
Cardiovascular
Psychiatry
Oncology
Neurology
Metabolic
Pain
Rare/Genetic
Immunology
Reproductive
Gastroenterology
Infectious Disease
Respiratory
Other Includes
- Women’s Health
- Rheumatology
- Endocrinology
- Dermatology
- Musculoskeletal
- Vaccine
Our Experience by Study Objective
Studies Completed
- Safety & Tolerability
- Alcohol Effect
- Irritation & Sensitivity
- Adhesion
- PPI Pre-Treatment
- Oral Tolerability/Palatability
%
First in Human of all Phase 1 Studies
BioPharma Services provides integrated support across clinical study planning and execution, including protocol development, regulatory submissions, participant recruitment, clinical conduct, bioanalysis, data management, biostatistics and final reporting.
Whether a sponsor is developing an innovative medicine, evaluating a new formulation or advancing a generic product, our team can provide the infrastructure and experience required to move the program forward.
Quality. Trust. Partnership.
We know how hard it can be to select the right CRO for your drug development program. That’s why we work so hard to ensure that from the moment you contact us to schedule a discovery call, we are with you for every step of the journey.
BioPharma Services is a full service CRO that can help you take your compound from the protocol development stage right through to submission to regulatory agencies.
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