|Articles|April 1, 2019

USP

USP’s Ingredient Verification Program for Excipients includes a complete evaluation of your quality system.

USP’s Ingredient Verification Program for Excipients includes a complete evaluation of your quality system. We take a holistic approach to excipient quality, incorporating a thorough review of your manufacturing batch records and product release data and offering an in-depth examination of how quality decisions affect your final product.

 

USP
12601 Twinbrook Parkway, Rockville, MD 20852
tel. +1.301.881.0666
CPhI North America Booth #2330


Related to this article

The BioPharm Brief: A $7 Billion Oncology Option Deal, a TL1A Pivot, and Oral Adalimumab Heads to the Clinic
Boehringer Ingelheim licenses six preclinical ADC and T-cell engager programs from Sino Biopharmaceutical in a deal worth up to $7 billion, Spyre Therapeutics drops anti-TL1A antibody SPY072 in rheumatic diseases after phase 2 misses and turns to hidradenitis suppurativa, and Biora Therapeutics gets ethics approval for a first-in-human trial of its BioJet oral adalimumab capsule.
The Promise of Microgravity for R&D and Manufacturing
As access to low Earth orbit expands, space-based research is opening possibilities in drug discovery, formulation, and manufacturing. In Part 1, the authors look at how microgravity changes biology and chemistry in ways that can’t be reproduced on Earth and where it fits from target discovery to life cycle management.