Ronald Piervincenzi, USP, explains why drug supply resilience needs a system approach, from procurement benchmarks to regulatory capacity building.
|Articles|March 2, 2018
VAI
VAI's manufacturing and testing operations mirror current GMP/GLP standards.
Advertisement
VAI’s manufacturing and testing operations mirror current GMP/GLP standards. With over 35 years of contamination control experience, our products and services include a comprehensive line of disinfectants, sporicides, residue removers, process cleaners, quality water, saturated and dry wipes, disposable garments, cleanroom paper, documentation materials, printing systems, viable monitoring, cleanroom cart systems, cleaning equipment, consulting, and laboratory services.
15 Lee Blvd, Malvern, PA 19355
tel. 610.644.8335
vai@sterile.com
INTERPHEX Booth #2527
Advertisement
Related to this article
Episode 1, Part 3 of PharmTech AI Pulse Check covers why INTerpath-001's AI isn't ChatGPT and names pharma manufacturing's biggest AI governance gaps.
Michael Levy, senior vice president, Digital & Innovation, USP, explains the digital supply chain in a preview of his upcoming CPHI Milan panel presentation, The Next Phase of Pharma Supply Chains.
FDA approves tavapadon, first D1/D5 agonist, validating AbbVie's $8.7B Cerevel deal and an October five-strength oral tablet launch.
Richard Jaenisch weighs how FDA's new NAM rule could reshape preclinical testing and what CMC teams should do now, on Manufacturing Intelligence.
In a preview of their panel discussion at AAPS PharmSci 360 2026, Alfred Rumondor, PhD, AbbVie, and Swita Singh, PhD, Bristol Myers Squibb, discuss the implementation of risk-based approaches for CMC.
Merck licenses SciBrunch's preclinical KRAS G12D inhibitor for $2.13B, raising tech transfer and scale-up questions for oral cancer drug development.
Ronald Piervincenzi, USP, urges drugmakers and purchasers to act on supply chain resilience to curb drug shortages and shape better policy.
Advertisement
Advertisement