At Aurora BioPharma, we offer a diverse portfolio of pharmaceutical solutions tailored to global healthcare needs.
Active Pharmaceutical Ingredients for major therapeutic segments
Your partner in crafting the future of pharmaceuticals
Impurities used in the production of high‑purity drugs.
Your vision, our expertise. Manufacturing made easy quality you can trust, service you can count on.
Innovating Chemistry Solutions
Precision in every step
Solutions in Solvents
Your Reliable Partner in International Trade
Established in 2018, Aurora BioPharma is a GMP‑ISO 9001:2015, and ISO 14001:2015‑certified company founded by Kirtee Wani along with a team of knowledgeable and experienced professionals dedicated to manufacturing actives, intermediates, specialty, and fine chemicals.
We understand that it is only by increasing the value of our customer satisfaction that we can build an ever-flourishing organization. What keeps us going & growing is the solid trust of our large customer base.
Our comprehensive capabilities, from compliance to consultation, drive innovation, scalability, and global delivery for healthier outcomes.
We adhere to global standards such as WHO-GMP and ISO to ensure quality, safety, and regulatory alignment across all our products.
With a strong foundation in chemistry, we scale products from lab to market—delivering innovation through process development and pilot trials.
Our infrastructure ensures secure, transparent, and timely product delivery worldwide, meeting client needs with agility and accuracy.
Our expert team collaborates closely with clients to support product development, regulatory dossiers, and custom synthesis at any scale.
At Aurora BioPharma, we integrate scientific excellence with streamlined delivery to provide cost-efficient, high-quality pharmaceutical solutions trusted worldwide.
We support a wide spectrum of sectors across the healthcare, pharmaceutical, and life sciences ecosystem—driving innovation, compliance, and access at every level.
We simplify the journey from molecule selection to market delivery guided by science, innovation, and regulatory precision.
Choose from a pre-vetted catalog or co-develop tailored formulations to meet your specific needs.
Work closely with our scientific and regulatory teams to align with global standards.
Leverage full-scale, GMP-certified production and seamless global logistics to ensure timely delivery.
Benefit from continued assistance—ranging from documentation and tech transfer to stability studies
Unsure about the ideal molecule, formulation approach, or regulatory pathway? Our experienced specialists are here to guide you at every stage from development to delivery.