Rethinking bioequivalence for nasal suspensions: Adopting an in-vitropathway with confidence
Discover how MDRS provides a regulatory-accepted alternative to clinical endpoint studies for nasal suspension bioequivalence. Learn to de-risk your ANDA pathway today.
Automating pMDI Actuation for Consistent In Vitro Bioequivalence Testing
Discover how automated pMDI actuation improves consistency and reduces analyst variability in in vitro bioequivalence testing, supporting realistic APSD analysis and FDA expectations.
Targeting accelerated progress at the IPAC-RS Nasal Innovation Forum 2025
Explore how Nanopharm presented strategies for accelerating patient-centric nasal product development at the IPAC-RS Nasal Innovation Forum 2025. Dive into key insights on regulatory science, advanced bioequivalence methods, and targeted drug delivery.
Aligning Alternative Bioequivilence with U.S. FDA: Advancing aerosol dose collection to enhance in vitro dissolution studies
Discover how Nanopharm’s DissoHale system advances aerosol dose collection and dissolution testing to support FDA-aligned alternative bioequivalence for OIDPs.
