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
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.
