The European Commission's anticipated package to revise European Unionpharmaceutical legislation was presented on July 18, and has been broadly welcomed by both the prescription and non-Rx industries.
Essentially, the objectives of three draft directives presented by the Commission are: to build on the success of the European Medical Evaluation Agency; increase and accelerate the availability of products; move with the times on better access to information for patients (see also page 12); improve the competitiveness of the European pharmaceutical industry in the world market; meet the challenges of an enlarged EU; and cut red tape.
Generics testing prior to patent expiry proposed
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