Abbott Laboratories (IL, USA) has agreed to acquire the pharmaceutical business of the Solvay Group (Belgium) for 4.5 billion Euros in cash.
Abbott Laboratories (IL, USA) has agreed to acquire the pharmaceutical business of the Solvay Group (Belgium) for 4.5 billion Euros in cash. The transaction also includes payments of up to 300 million Euros if certain sales milestones are met between 2011 and 2013. Abbott will also assume certain liabilities, mainly pensions, valued at EUR 400 million, according to a Solvay press release.
"The acquisition of Solvay Pharmaceuticals further diversifies our pharmaceutical portfolio, expands our presence in key high-growth emerging markets, enhances our investment in R&D and accelerates our long-term earnings-per-share growth outlook," said Miles D. White, Chairman and CEO of Abbott, in the company’s release.
Solvay Pharmaceuticals posted 2008 sales of 2.7 billion Euros, according to the Solvay press release. It employs 9000 people worldwide. Its key areas of therapeutic focus are neuroscience, cardiometabolic, influenza vaccines, gastroenterology, and men's and women's health. The acquisition also includes full global rights to the fenofibrate franchise. Currently Abbott has US rights to fenofibrate and pays royalties to Solvay. Solvay also has a small molecular diagnostics unit that will become part of Abbott's diagnostics organization upon the close of the transaction. This transaction is subject to customary closing conditions and regulatory approvals and is expected to close in the first quarter of 2010.
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.