Articles by Stephanie Sutton - Pharmaceutical Technology

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Articles by Stephanie Sutton

EMA Aims to Facilitate Biosimilars Development

Oct 1, 2012

The European Medicines Agency has updated its guidance on biosimilar medicines, with the aim of helping companies to avoid unnecessary repetition of clinical trials.

Sanofi to Cut 900 Jobs

Sep 27, 2012

Sanofi is planning to shed approximately 900 jobs in France in the lead up to 2015 as it seeks to implement certain key strategic objectives.

EMA Streamlines Working Parties

Sep 25, 2012

The European Medicines Agency has abolished its Cell-based Product Working Party and Gene Therapy Working Party, with the aim of improving efficiencies and optimizing the use of available expertise.

Great Expectations for CPhI Worldwide 2012

Sep 20, 2012

This year's CPhI Worldwide event is set to take place at the Feria de Madrid in Spain, October 9-12, with expectations for more than 30000 visitors and 2200 exhibitors from 140 countries.

J&J to Establish Innovation Centers

Sep 19, 2012

Johnson & Johnson has announced plans to open four innovation centers in California, Boston, London, and China, with the aim of accelerating early innovation and facilitating collaboration and investment opportunities.

Potential European Pharmacovigilance Fees Criticized

Sep 18, 2012

The European Generic Medicines Association (EGA) has raised concerns about the potential fees to be charged by the European Medicines Agency for pharmacovigilance activities

Eli Lilly Receives FDA Warning Letter

Sep 10, 2012

Eli Lilly has received an FDA Warning Letter because of a "misleading" image of a multicolored brain that appeared on the company's website for the diagnostic PET tracer, Amyvid.

Merck KGaA to Reduce 10% of its German Workforce

Sep 5, 2012

Merck KGaA has announced plans to eliminate 1100 jobs in Germany by the end of 2015—almost 10% of the company's 10,900 German positions.

Industry Gears up for GDUFA

October will see the implementation of FDA's Generic Drug User Fee Amendments of 2012.
Sep 4, 2012

Generic-drug manufacturers are preparing to pay fees to FDA for the first time in the agency’s history.


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Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
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Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
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