On 19 December 2016, the European Medicines Agency (“EMA”) published an updated version of the EMA guidance document concerning post-authorisation procedural advice for users of ...24 January 2017
Drug pricing myths and realities
MYTH: It’s all about profit.
REALITY: “Drug manufacturers want to be part of the solution, and they’re always looking at ways they can offer value-based pricing to the marketplace,” says Roberts. “[But] the regulatory environment – and the many laws that affect pricing – can make that challenging.”
MYTH: It’s a U.S. problem.
REALITY: “While a lot of the media attention is focused on the U.S. market, countries all over the world are struggling with how to pay for specialty pharmaceuticals and how to finance cures within our health care systems,” Roberts says. “There is no question that this is a pressing issue around the globe.”
MYTH: It shouldn’t be a political issue.
REALITY: “It’s important for drug manufacturers to have a seat at the table and for their voices to be heard,” Roberts says. “They need to be able to talk about the value of their products… the value of cures, the value of medical innovation, and the fact that we all need to find a way that the cures can be affordable to both governments and patients.”
MYTH: Drugs cost too much, period.
REALITY: “I think we, as a society, need to look carefully at how we pay for innovation,” Roberts says. “When you compare drug prices to the cost of having someone sick in the hospital, missing work, or dying prematurely from cancer, you realize what a complex, challenging issue it is.”
Watch the below video to hear what Beth Roberts views as some of the most common misconceptions related to the crucial issue of drug pricing in this exclusive video interview.
Regulation (EU) No 536/2014 of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC (“the Clinical Trials Regulation”) was...24 January 2017
The UK Medicines and Healthcare products Regulatory Agency (“MHRA”) has published a draft strategy for developing pharmacopoeial public quality standards for biological...20 January 2017