The European Generic Medicines Association (EGA) is calling for an urgent reform of the European patent system; in particular, the agency stresses that the quality of patent examinations and applications should be improved, and that examination and opposition proceedings should be accelerated.
The European Generic Medicines Association (EGA) is calling for an urgent reform of the European patent system; in particular, the agency stresses that the quality of patent examinations and applications should be improved, and that examination and opposition proceedings should be accelerated.
Speaking at the 6th EGA legal affairs forum held in Munich (Germany) last week, Greg Perry, Director General of the EGA, said: "If the patent system is not reformed in Europe, drug manufacturers will encounter increasing hurdles to competition and real innovation."
The importance of the patent system was highlighted in the European Commission's Pharmaceutical Sector Inquiry, which was launched in 2008 to identify why so few novel medicines were being brought to market. The final report, released in 2009, called for the strengthening of the European patent system and also suggested the establishment of a single European patent. Both views were supported by the European Patent Office (EPO), which has been trying to "raise the bar" to help end patent uncertainty.
In a press statement, the EGA said that it supports the EPO's efforts and also backs the introduction of an Information Disclosure Statement, a requirement for applicants to provide the results of earlier relevant patent office searches to aid the European examination procedure.
However, there are some issues that the EGA remains concerned about. Firstly, the agency is worried about the possibility of evading EPO rules that limit the filing of divisional applications. Additionally, the EGA adds that patent litigation discrepancies across Europe are problematic. "This disparity could be solved by the establishment of a well-balanced, central European Patent Court with technically qualified experienced judges," said the press statement. "This would create an opportunity to streamline and simplify patent disputes."
Following on from the inquiry, the EGA has said that it will continue dialogue with the EPO with the aim of improving the efficiency of the patent system in line with proposals from the European Commission.
Perry said: "The follow up to the Pharmaceutical Sector inquiry is now clearly taking place. Recent moves by the European Commission's DG competition to investigate actions that hinder the market entry of generic citalopram and Spain's move to accelerate pricing decisions for generic medicines are evidence of this."
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.