Amsterdam, 2 July 2015
Joint response to an EMA public consultation. The European Medicines Agency (EMA) and Heads of Medicines Agencies (HMA) are in danger of failing to address urgent public health needs due to a lack of independence and transparency.
> Click here to download the Joint Response (pdf, 824 Ko)
> Click here to download the Press Release (pdf, 122 Ko)
Press release
The European Medicines Agency (EMA) and Heads of Medicines Agencies (HMA) are in danger of failing to address urgent public health needs due to a lack of independence and transparency, Health Action International, the International Society of Drug Bulletins and the Medicines in Europe Forum warned today.
The coalition expressed its concerns in a public consultation response to the EU Medicines Agencies' Network Strategy to 2020.
Ancel.la Santos, policy advisor with Health Action International, said the projection that 83 percent of the EMA's budget will come from corporate fees in 2015 is major cause for concern.
"The EMA must lead by example and make independence its clear priority," said Santos. "Reliance on fee-for-service sets up a customer/provider relationship between the regulator and the regulated. Direct financial relations between the EMA and industry must be phased out. Protecting patients is a public task that should be directly financed from the EU budget without strings attached."
The health NGOs also stated that independence of medicines agencies also relies on the implementation of strong conflicts of interest policies for staff and experts.
"The recent weakening of the EMA's conflicts of interest policy for experts is a strong indication that the problem is being underestimated," said Pierre Chirac, coordinator of the Medicines in Europe Forum.
Chirac also warned that "the provision of customised, confidential scientific advice from medicines agencies to companies holds an inherent risk of regulatory capture. At a minimum, committee members deciding on marketing authorisation shouldn't be involved in providing advice, and detailed reports of these interactions should be made available."
The coalition also calls for the medicines agencies to prevent adaptive pathways from becoming the rule rather than the exception.
"Too many medicines are being given premature licensing at the expense of proper evaluation," said Jörg Schaaber, president of the International Society of Drug Bulletins. "If no genuine unmet medical need is at stake, accelerated approval should not be used to prevent unnecessary exposure to avoidable harm. Instead of lowering the bar, new drugs must show benefits that matter to patients – this is today often not the case."
The group also urged competent authorities and medicines agencies to comply with clinical data transparency requirements because they are crucial to assess the true benefits and harms of treatments. This data must be considered a public good and not commercially confidential.
Further details are available in the Coalition's full consultation response (link below).
For comment and additional information:
Ancel.la Santos Quintano, Policy Advisor, Health Action International
Phone: +31 20 683 3684 - Email: ancel.la@haieurope.org - Web: www.haieurope.org
Pierre Chirac, Coordinator, Medicines in Europe Forum
Email: pierrechirac@aol.com - Web: http://english.prescrire.org
Jörg Schaaber, President, International Society of Drug Bulletins
Email: press@isdbweb.org - Web: www.isdbweb.org
©HAI, ISDB, MiEF July 2015
> Click here to download the Joint Response (pdf, 824 Ko)
> Click here to download the Press Release (pdf, 122 Ko)
