Articles by Susan Haigney - Pharmaceutical Technology

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Articles by Susan Haigney

EMEA Recommends Two H1N1 Vaccines for Authorization

Oct 1, 2009

On September 25, the European Medicines Agency's (EMEA) Committee for Medicinal Products for Human Use (CHMP) recommended the authorization of two vaccines for use in Europe against the H1N1 influenza: GlaxoSmithKline's (GSK) Pandemrix and Novartis's Focetria.

GlaxoSmithKline and Pfizer Create New HIV-Focused Company

Apr 23, 2009

Pharmaceutical giants GlaxoSmithKline (GSK) and Pfizer announced on April 16, 2009 that they are joining forces to create a new HIV-focused drug company.

Growth of US Prescription Sales Slow in 2008

Mar 26, 2009

On March 19, 2009, IMS, the leading provider of market research for the pharmaceutical and healthcare industries, reported that annual sales of prescriptions in the US grew 1.3% from 287.6 billion in 2007 to 291.5 billion in 2008.

Governor Kathleen Sebelius Nominated for Secretary of HHS

Mar 5, 2009

President Obama nominated Kansas Governor Kathleen Sebelius as his new Secretary of Health and Human Services (HHS).

FDA Comments on ICH Q4B Draft Annexes

Feb 26, 2009

The US Food and Drug Administration stated its considerations in regards to the three draft annexes to the International Conference on Harmonization's Q4B document.

Congressman Questions FDA's Heparin Investigation

Nov 26, 2008

In a letter to Acting Comptroller General Gene Dodaro dated November 19, 2008, Congressman Joe Barton (R-Texas) requested that the US Government Accountability Office (GAO) review the US Food and Drug Administration's handling of the highly-publicized, tainted heparin scare that occurred in 2007 and 2008.

FDA Outlines Rules on Genetically Engineered Animals

Sep 25, 2008

In an effort to clarify its policy on the use and creation of genetically engineered animals (GE animals), the US Food and Drug Administration released the draft guidance "The Regulation of Genetically Engineered Animals Containing Heritable rDNA Constructs" on September 18.

FDA Issues Warning Letters and Import Alert on Ranbaxy Laboratories

Sep 18, 2008

The US Food and Drug Administration has issued two warning letters to Ranbaxy Laboratories.

FDA Updates Bioequivalence Guidelines

Sep 11, 2008

The US Food and Drug Administration has updated its draft bioequivalence recommendations for several products, and added 66 new draft product-specific guidelines since October 2007.

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