The regulation will entitle EU-based companies to manufacture a generic or biosimilar version of an SPC-protected medicine during the term of the certificate, if done either for the purpose of exporting to a non-EU market where protection has expired or never existed, or for stockpiling during the final 6 months of an SPC ahead of entry into the EU market. It will thus remove a major competitive disadvantage of EU manufacturers compared to manufacturers based in non-EU countries and ensure a better deal for patients.
The revision is a well-calibrated adjustment to the current regime striking a balance between ensuring the attractiveness of Europe for innovative pharmaceutical companies and allowing EU-based generics and biosimilar to compete on the global market. This manufacturing waiver will help create growth and high-skilled jobs in the EU and could generate more than €1 billion net additional sales per year and up to 25,000 new jobs over 10 years, particularly benefitting SMEs. More competition will improve patients’ access to a wider choice of medicines and alleviate public budgets.
Today’s vote amends EU Regulation 469/2009 on the supplementary protection certificate for medicinal products. The text now needs to be formally endorsed by the Council of the European Union. Once published on the Official Journal of the EU, the regulation will enter into force in 20 days. It will be directly applicable in all EU countries. The full effects of the SPC waiver will be felt from 3 years after the date of that entry into force.
EU and global pharmaceutical markets are undergoing profound changes. Global demand for medicines has increased massively, reaching over €1 trillion in 2017. Alongside this, there is a shift towards an ever-greater market share for generics and biosimilars. Traditionally the EU has played a pioneering role in pharmaceutical research and development, including generic medicines and biosimilars. But this leadership position is under threat…