15 September 2009
The Innovative Medicines Inititative (IMI), the public-private partnership between the European Commission and the European pharmaceutical industry, has announced the topics for research for its second call for proposals.
Funding of 156.3 million will be made available, 76.8 million coming from the European Commission and 79.5 coming from EFPIA member companies.
The topics are as follows:
Imaging biomarkers for anticancer drug development
New tools for target validation to improve drug efficacy (oncology)
Molecular biomarkers: accelerating cancer therapy development and refining patient care.
Indentification and development of rapid point of care diagnostic tests for bacterial diagnosis to facilitate conduct of clinical trials and clinical practice
Understanding aberrant adaptive immunity mechanisms
Translational research in chronic immune-mediated disease: bridging between animal models and humans
Drug/disease modelling: library & framework
Open pharmacological space
Electronic Health Records
The IMI has also announced the appointed of a new executive director, Professor Michel Goldman. Commenting on his appointment he said: "I am very please to be joining IMI at such an exciting moment in its development. On the basis of my previous experience in public-private partnerships, my first priority will be to strengthn the bridges between academia andindustry in the interest of patients."
CEO of Bayer Healthcare and President of EFPIA, Arthur J. Higgins commenting in a press release, said: "The IMI is a clear statement that Europe intends to be at the forefront of biopharmaceutical innovation. By accelerating and optimising R&D processes we are trying to remove bottlenecks in the drug development process...The greatest success of this initiative has been bringing together normally competing pharmaceutical companies with academic stakeholders in an unparalleled effort to accelerate the discovery of innovative medicines."
Beyond the Prescription: Pharma's Role in Digital Health Conversations
April 1st 2025Join us for an insightful conversation with Jennifer Harakal, Head of Regulatory Affairs at Canopy Life Sciences, as we unpack the evolving intersection of social media and healthcare decisions. Discover how pharmaceutical companies can navigate regulatory challenges while meaningfully engaging with consumers in digital spaces. Jennifer shares expert strategies for responsible marketing, working with influencers, and creating educational content that bridges the gap between patients and healthcare providers. A must-listen for pharma marketers looking to build trust and compliance in today's social media landscape.