SCCR22: Opening statement of the Development Agenda Group
Development Agenda Group’s Statement
22nd session of the Standing Committee on Copyright and Related Rights
(15-24 June 2011)Mr. Chairman,
Opening statement of Uruguay at WIPO’s 22nd Standing Committee on Copyright and Related Rights
Comité Permanente de Derechos de Autor y Conexos – SCCR 22 – OMPI – Ginebra
Intervención de la Delegación de Uruguay. Ginebra, 15 de junio de 2011.Gracias Señor Presidente,
Señor Presidente, reciba de nuestra delegación nuestras mas sinceras felicitaciones por su designación como Presidente del Comité Permanente de Derechos de Autor y Conexos SCCR y cuente con nuestro apoyo para hacer una exitosa gestión al frente de este importante comité.
Señor Presidente:
White House and European Commission trade official oppose waiver of drug patents for Least Developed Countries (LDCs)
KEI Policy Brief 2011:1
June 11, 2011, Revised August 15, 2011Pharmaceutical global R&D was 7.9 percent of sales in 2010
Using industry assertions of R&D spending, pharmaceutical related R&D spending by the private sector was less than 8 percent of global sales in 2010.
These are the data:
2010 Global R&D by all private companies: – $67.4 billion
Source: Page 2 of the 2011 PhRMA industry profile
http://report.nih.gov/investigators_and_trainees/acd_bwf/pdf/Phrma_Industry_Profile_2011.pdf2010 Global sales – $856 billion
Continue ReadingKEI Intervention at UN HLM on HIV: De-Linking R&D costs from drug prices and the sustainability of treatment
These are the notes from my intervention today at the UN’s High Level Meeting on HIV/AIDS in New York. The persons making statements from the floor were asked to keep their comments to two minutes, so the actual intervention was somewhat shorter. Jamie
2011 High-Level Meeting on
the comprehensive review of the progress achieved in realizing
the Declaration of Commitment on HIV/AIDS and
Continue ReadingDraft of the Political Declaration on HIV and AIDS disappoints public health NGOs
NYC, 7 PM Wed, June 8, 2011.
FDA New drug approvals for 2011, through June 6
This is a report from the FDA on 2011 new molecular entities (NMEs) approvals, through June 6, 2011. The total number of FDA approvals during that same period was 150. So far, 16 NMEs have been approved in five months, a sharp increase in approvals over the same period 2010.
6 NMEs NDAs were considered priorities
8 NDAs that were considered standard approvals
2 BLA (biologic products) that were not classified.
- NMEs were 10.7 percent of all approvals.
- The NME priority NDAs were 4 percent of FDA approvals.
WHO Executive Board Decision 129(8): WHO reform for a healthy future
On Wednesday, 25 May 2011, the 129th session of the World Health Organization’s Executive Board approved Decision, EB129(8) on “WHO reform for a healthy future”. Reproduced below is the text of the Decision which is yet to be published on the WHO website in all 6 UN languages.
EB129(8) WHO reform for a healthy futureThe Executive Board,
Karl De Gucht writes Andris Piebalgs on topic of European Union IPR demands on India and other developing countries
KEI has received a copy of a May 16, 2011 letter from Karl De Gucht to Andris Piebalgs, which discusses (1) the EU-India FTA, and (2) Relations between IPR and development policies. Continue Reading
Senator Sanders introduces two medical innovation prize bills in U.S. Senate to de-link R&D costs from drug prices
On Thursday, May 26, 2011, Senator Bernie Sanders (I-VT) introduced two bills in the United States Senate that would de-link R&D costs from drug prices. The bill names and numbers are as follows: