TUV SUD Acquires MSOURCE to Enter Life Science Clinical Research
TUV SUD has completed the acquisition of all shares of MSOURCE Medical Development to create a new T?V S?D Life Science business unit.
TUV SUD acquires MSOURCE to enter life science clinical research
TUV SUD has completed the acquisition of all shares of MSOURCE Medical Development to create a new TUV SUD Life Science business unit. MSOURCE will be the contract research organization (CRO) of this business unit, which will belong to the PEOPLE division of TUV SUD. TUV SUD’s dedication to product reliability, safety and quality now extends to the pharmaceutical and biotechnology industries. To the medical device industry, TUV SUD now additionally offers clinical research services.
MSOURCE employs more than 240 personnel, active in clinical trial management, data management, statistics, pharmacovigilance and quality assurance on behalf of pharmaceutical, biotechnology and medical device companies. Currently services are delivered from headquarters in Brussels/Kraainem and offices in the Netherlands, Germany, Poland, Spain and the UK.
“The opportunity to apply TUV SUD’s certification, testing and management skills to clinical research services is the main reason to make this important step forward,” said Prof. Dr. Peter Schaff, managing director of TUV SUD’s PEOPLE Division. “There is a distinct need for quality in each step of the clinical research process, while the complexity and global reach of clinical trials increase every year.
“We are creating an important new Contract Research Organization with the stability of a major company, combined with the flexibility and responsiveness of a mid size CRO,” said Dr. Adriaan Hart de Ruijter, co founder and managing director of MSOURCE. “We made the choice for TUV SUD because of a shared vision on quality and future strategy. The access to worldwide facilities and capital enables us to respond better to our client’s needs”. Dr. Hart de Ruyter assumes the role of managing director, TUV SUD Life Science, and will continue to lead the management team of MSOURCE as well as the further expansion to achieve global reach. MSOURCE will remain an independent organization and entity in the TUV SUD group. The headquarters of MSOURCE will remain in Kraainem, close to Brussels.
“Our employees will fit well into the PEOPLE division of TUV SUD. MSOURCE’s mission to deliver excellence in clinical research services is close to TUV SUD’s original corporate mission to support the design of technology for the benefit of people,” said Dr. Anne Jolie, co founder and Manager Pharmacovigilance & Medical Affairs at MSOURCE.
SOURCE TUV SUD
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
The Rise of Predictive Engagement Tools in Clinical Trials
November 22nd 2024Patient attrition can be a significant barrier to the success of a randomized controlled trial (RCT). Today, with the help of AI-powered predictive engagement tools, clinical study managers are finding ways to proactively reduce attrition rates in RCTs, and increase the effectiveness of their trial. In this guide, we look at the role AI-powered patient engagement tools play in clinical research, from the problems they’re being used to solve to the areas and indications in which they’re being deployed.
