Displaying 1–24 of 24 results for USP
Questions about product sterility due to microbial growth have caused Pfizer's Hospira to issue a large recall of various injectables distributed from January to June 2017.
PDA has been approved by ANSI to be an ASD because PDA’s portfolio of technical reports includes many topics that are good candidates to become American National Standards
AUVI-Q (epinephrine injection, USP) auto-injector will enter the U.S. market in the first half of 2017
Although still not inexpensive, Mylan will offer a generic to its EpiPen Auto-Injector at a list price of $300 per two-pack carton
The company announced the U.S. launch of Doxycycline Hyclate Delayed-Release (DR) Tablets USP, 50 mg
Due to the presence of a particulate, Hospira is voluntarily recalling one lot of 8.4% Sodium Bicarbonate Injection, USP
The product contains an inactive ingredient that may cause nasal burning if OXAYDO is manipulated
This product is a combination penicillin-class antibacterial and beta-lactamase inhibitor
Baxter International Inc. announced on December 23 thatit has initiated a voluntary recall to the hospital/user level of one lot of 5% Dextrose Injection, USP and four lots of 0.9% Sodium Chloride Injection, USP due to particulate matter found in the solutions.
CPhI Conferences announces a three-day technical conference, Quality by Design, taking place from 25 - 27 November 2013 in Kuala Lumpur, Malaysia.
Vial defect may cause particulate to enter solutions
Altaire Pharmaceuticals, Inc. is voluntarily recalling a total of nine lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution, 30 mL, to the consumer level due to complaints of mold found in the 30 mL bottles after use.
Ready-to-submit documentation for the USA and Europe, and now Japan
BD Enters Pharmaceutical Industry with New Line of Generic Prefilled Injectable Products
Becton, Dickinson and Company announced that the FDA has approved the first drug to be offered in the just-launched BD Simplist ready-to-administer, line of prefilled generic injectables.
USP Board of Trustees initiates transition process of CEO Roger L. Williams in accordance with previously agreed contractual commitments
USP will use Thermo Scientific TruScan RM and microPHAZIR RX instruments to develop raman and NIR libraries for pharmaceutical manufacturers
CDER Director Dr. Janet Woodcock Will Keynote Workshop, Modernized Standards to have Broad Patient, Industry Impact
USP has re-evaluated the currently available Prednisone RS Tablets Lot P0E203 and established new acceptance criteria based on a whole-assembly geometric mean and standard deviation approach rather than the individual-position (per tablet) approach.
To promote international scientific exchange and ultimately foster global harmonization of standards for medicines and food ingredients, scientists from around the world will join the U.S. Pharmacopeial Convention (USP) at its headquarters on a rolling basis throughout 2010. USP welcomed the ...
Celsis has expanded the analytical chemistry capabilities of its cGMP labs to include Mass Spectrometry (LC-MS/MS) and Ion Chromatography.
Re-evaluated Material, New Approach and Calculation Tool to Help Pharmaceutical Manufacturers Comply with Quality Standards
The first results from a large-scale study of key antimalarial medicines in ten Sub-Saharan African countries reveal that a high percentage of medicines circulating on national markets are of substandard quality and thus may contribute to the growth of drug-resistant strains of Plasmodium ...