Reports

Generics saved US healthcare system and patients US$1 trillion

Home/Reports | Posted 10/08/2012

According to a new report from the Generic Pharmaceutical Association (GPhA), released on 2 August 2012, generics saved the US healthcare system and patients US$1 billion every other day―totaling US$193 billion in 2011 and more than US$1 trillion over the last 10 years (2002–2011).

Rise in US spending on generics: a buoyant market as patents expire on brand-name drugs

Home/Reports | Posted 22/06/2012

A new IMS report notes a rise in spending on generic medicines in the US to 27%, or US$75 billion, and looks at the main changes driving the trend.

More capacity needed in clinical trial review for national approval of biosimilars

Home/Reports | Posted 22/06/2012

The need for National Regulatory Authorities to build capacity in clinical trials review, and for WHO to continue monitoring regulatory procedures for the evaluation of biosimilars were among the main recommendations of a workshop to discuss the implementation of WHO guidelines on evaluating biosimilars in Seoul, Republic of Korea, 24–26 August 2010.

WHO guidelines on biosimilars: case studies and discussion highlights

Home/Reports | Posted 18/06/2012

The experiences and progress of different countries in implementing WHO guidelines on evaluating biosimilars were the focus of a workshop hosted jointly by WHO and Korea Food and Drug Administration (KFDA).

Global generics markets predicted to grow to US$221 billion by 2016

Home/Reports | Posted 04/05/2012

The global markets for generic drugs will continue to grow despite cost reduction measures from governments and healthcare payers in many markets.

Biosimilars marketed in Europe

Home/Reports | Posted 18/05/2012

Europe was the first region to approve and introduce biosimilars into the market back in 2006, and now in 2012 the continent is the largest biosimilars market in the world, with 14 biosimilars approved by EMA.

Biosimilars use in Europe

Home/Reports | Posted 25/11/2011

A legal framework for approving biosimilars in the EU was established in 2003 and guidelines for an abbreviated registration process were issued in 2006. However, acceptance and use of biosimilars within Europe varies by country.

Oncologists inconsistent in how they judge value of high-cost cancer drugs

Home/Reports | Posted 27/04/2012

A survey of oncologists in Canada and the US has shown that physicians are inconsistent when deciding how long an expensive new cancer therapy should extend a person’s life before the cost of the therapy is justified. The results of the survey also showed the benefit that oncologists demand from new treatments in terms of length of survival does not necessarily increase according to the price of the treatment [1].

AARP report highlights importance of generics

Home/Reports | Posted 16/03/2012

According to a report issued on 6 March 2012 by AARP (formerly the American Association of Retired Persons) the prices of drugs used most widely by older Americans rose by nearly 26% from 2005 to 2009 or in other words nearly twice the rate of inflation.

UK gets value for money for its medicines

Home/Reports | Posted 02/03/2012

A UK Department of Health (DoH) report confirms that the voluntary pricing agreement between the DoH and the pharmaceutical industry is working and that medicines are good value for money for the National Health Service (NHS).