Process Validation

May 19, 2014
By Pharmaceutical Technology Editors
Hospira has recalled one lot of labetalol hydrochloride injection, USP, due to visible particulates.
Feb 25, 2014
PTSM: Pharmaceutical Technology Sourcing and Management
By Pharmaceutical Technology Editors
Daiichi Sankyo announced suspension of API shipments from Ranbaxy's Toansa and Dewas plants; issues apology to stakeholders.
Jan 24, 2014
By Pharmaceutical Technology Editors
FDA adds Ranbaxy's Toansa, India facility to existing consent decree, prohibiting distribution of APIs from that location
Jan 22, 2014
By Pharmaceutical Technology Editors
Online portal accepts nominations for FDA advisory committee membership.
Jan 08, 2014
By Pharmaceutical Technology Editors
EMA has launched a new version of the EudraGMDP database, which includes the publication of statements of non-compliance with good manufacturing practice.
Jan 02, 2014
Pharmaceutical Technology
Antibody fragments pose unique challenges in terms of recovery, purification, and formulation.
Nov 15, 2013
By Pharmaceutical Technology Editors
Covance Inc. and Pathoquest have announced a collaboration to provide next-generation sequencing (NGS) based biosafety assessments to detect and identify viral contaminants within biologic compounds.
Oct 28, 2013
By Pharmaceutical Technology Editors
Zhoydro ER is the first drug to have updated labeling now required for all ER/LA opioid analgesics.
Oct 22, 2013
By Pharmaceutical Technology Editors
FDA is seeking a permanent injunction against a dietary supplement manufacturer following the company?s repeated distribution of unapproved drugs and adulterated dietary supplements.
Oct 07, 2013
By Pharmaceutical Technology Editors
During the ongoing federal government shutdown, FDA activities will be limited to work involving the safety of human life or the protection of property, and activities funded by carryover user fee balances PDUFA, GDUFA, and MDUFA.
native1_300x100
lorem ipsum