About Us
At Aroga Biosciences
We are a full-service medical writing and regulatory operations partner dedicated to supporting life sciences companies through every stage of development—from first-in-human studies to global submissions. Our name, Aroga, means “free from disease”—reflecting our commitment to helping bring safe and effective therapies to patients, faster.
Founded by scientists, Aroga brings together deep regulatory knowledge, rigorous quality standards, and an agile, collaborative spirit. Whether you need clinical and regulatory documents, expert-level QC, or eCTD-ready publishing, our team works seamlessly with yours to deliver excellence without compromise.
We don’t just write documents—we tell data-driven stories that stand up to regulatory scrutiny and accelerate development.
Aroga Team
Our team is made up of scientists first—PhDs, PharmDs, and advanced-degree professionals with years of experience in clinical, nonclinical, and regulatory strategy. We pride ourselves on being not just writers, but scientific partners who understand the “why” behind every project.
- Experienced in all major document types, from INDs, IBs, protocols, and CSRs to Module 2/Module 5 summaries and submissions.
- Therapeutic area expertise across oncology, rare diseases, neurology, infectious disease, and more.
- Rigorous QC and compliance standards, driven by our internal SOPs and client-specific requirements.
- Fully remote and global-ready, with staff across Pacific, Central, and Eastern time zones.
We also believe in mentorship, continuous learning, and collaboration. Our writers and QC professionals regularly attend AMWA and DIA conferences, contribute to internal trainings, and present at industry events—ensuring our clients benefit from the latest trends and best practices.
With Aroga, you are gaining a dedicated scientifically trained partner committed to the success of your therapeutic development programs.
Aroga Management
