This week, the FDA opened applications for its Expedited IND Pilot, quality experts presented at the PDA/FDA Joint Regulatory Conference, and Hovione expanded its spray drying capacity.
|Articles|February 8, 2022
How to Increase Productivity and ROI in Biopharma Laboratories
Author(s)PHC Corporation, Biomedical Division
Pressure for innovative products is becoming greater for pharmaceutical companies as they spend a significant amount on R&D and ways to achieve ROI in biopharma labs.
Related to this article
Christy Owings, Thermo Fisher, explains clinical trial supply chain risks in Latin America, importer-of-record strategy, AI, and eCOA delays.
PharmTech AI Pulse Check debuts: pharma experts tackle GxP 'slop,' multi-agent validation risk, OCR document mining, personalized mRNA cancer therapy.
Andrea K. Kerrigan, FDA, outlines how validation, data integrity, and QRM determine whether digital tools and AI strengthen or undermine CGMP compliance.
PharmTech spoke with Tara Dougal, event director for pharma at Informa Markets, about trends impacting the pharmaceutical industry and how CPHI Milan is addressing these areas this year.
Andrew Parker, PhD, executive drug development consultant, Quotient Sciences, explains how AI is integrated into pharmaceutical development.
PDA/FDA 2026 session maps the GMP audit lifecycle, root cause to CAPA closure, plus a local vs. above-site decision framework and two case studies.
The recently opened NJ spray drying facility doubles capacity for amorphous solid dispersions, addressing solubility limits in roughly 70% of small-molecule pipelines.
Trending on Pharmaceutical Technology
1
Introducing the "PharmTech AI Pulse Check" Expert Video Series
2
PharmTech Weekly Roundup—September 18, 2026
3
Can AI Agents Satisfy CGMP Documentation Requirements?
4
Two Audit Case Studies Reveal the Cost of Incomplete Corrective Actions
5