In pharma delivery, size matters. So, too, do the intricacies of dosage
format, active ingredient compatibility, and effective delivery to
patients—whatever their needs or preferences may be.
Yet standard dosage forms haven’t always provided companies the
options, flexibility, or performance to bring all those puzzle pieces
together during therapeutic development.
We spoke with Nathan H. Dormer, PhD, Director of Drug Product
Development at Adare Pharma Solutions, to learn how this new
technology platform is expanding the frontiers of therapeutic delivery
and improving patients’ experience in the process.
Panelists on PharmTech AI Pulse Check debate SURPASS, a new digital-twin trial program, regulatory acceptance, and the data-cleanup burden it will create.
Boyang Wang of Immortal Dragons explains how FDA's Expedited IND Pilot and QRIs could compress sequential first-in-human steps as China's Decree 818 raises the pace.
The FDA expanded Anktiva to BCG-unresponsive papillary-only NMIBC using existing CIS trial data, a precedent with implications for development timelines and supply planning.
Ishani Maharaj of Ingredients + Specialties from Univar Solutions explains how to stabilize GLP-1 multi-agonists, weigh delivery formats, and qualify novel excipients and suppliers.