QbD Group
Louise Buelens is a seasoned legal professional currently working as a Paralegal - Contract Associate at QbD since March 2023. Prior to this role, Buelens served as an Advocaat in opleiding at KONSILIO Advocaten from September 2021 to April 2023 and gained valuable experience as an intern at the Openbaar ministerie in September 2019. Buelens holds a Master's degree in Forensics, Criminology and Law from Maastricht University (2020-2021) and a Master's degree in Criminal Law from KU Leuven (2018-2020). Additional academic credentials include a Master's exchange semester in Law at the University of Montpellier (2018) and a Bachelor's degree in Law from KU Leuven (2015-2018). Buelens completed secondary education with a High School Diploma in Latijn Wiskunde at Sint-Gummarus College (2009-2015).
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QbD Group
The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. We are a multinational company with over 450 high-qualified employees. Our experienced team serves the wider life science industry, with a strong focus on ATMPs, medical devices, IVDs, and digital health, thanks to the specific expertise we have built in these areas. The services we offer fall under the following divisions: • Regulatory Affairs: We help our clients in their journey throughout the entire drug and medical device regulatory lifecycle. • Clinical: We are an expert clinical solutions provider specialized in medical devices and biotech, offering global CRO services and consultancy. • Qualification and Validation: We guarantee that products meet quality demands and comply with regulation through the qualification and validation of your processes, equipment, and software. • Quality Assurance: We offer the full range of QA services necessary to get your product to market in a safe and compliant way, including auditing from certified auditors, setting up your QMS, and all QP (Qualified Person) activities. • Quality Control: Our QC division consists of a GMP laboratory that offers analytical services for testing pharmaceutical raw materials, excipients, and release testing of finished products. • Software solutions: Cloud-based and pre-validated Quality Management Software built for the life sciences, as well as eIFU services which enable IVD and MD manufacturers to digitalize paper Instructions For Use (IFU). • Go to market: We help you launch your product to market by providing marketing and communication services, business development support and sales strategy.