New European legislation designed to protect patients is delaying clinical trials
The trade group European Federation of Pharmaceutical Industries and Associations (EFPIA) has slammed recent new regulations, saying they delay medical research.
It says that new legislation designed to improve public health and protect patients has unforeseen implementation effects that are delaying clinical trials and blocking access to new treatments for conditions like cancer and rare diseases.
The number of clinical trials delayed is expected to run into the hundreds, affecting up to 42,200 patients over the next three years, according to a survey run by EFPIA. The legislation is also likely to result in delays to therapies reaching patients in Europe. The EFPIA is urging all partners to enter talks to find solutions and mitigate the negative unintended impact of the legislation.
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