QbD Group
Tom Lokermans has extensive work experience in finance and leadership roles. Tom started their career as a Financial Auditor at PricewaterhouseCoopers in 2003. In 2006, they joined Ontex as a Manufacturing Controller and worked there until 2009. At Colfridis Invest nv, they served as a CFO from 2009 to 2017, where they were responsible for financial reporting, planning, budgeting, treasury, consolidation, and compliance. From 2017 to 2019, they worked as a CFO at Vulpia, and since 2019, they have been working as a CFO at QBD.
Tom Lokermans has a diverse education history. In 1998, they began their studies at KU Leuven, where they pursued a Master's degree in applied economics. Tom successfully completed this program in 2003. Later, in 2013, they attended Vlerick Business School, where they enrolled in the Executive Master class in corporate finance. This program lasted until 2014.
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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.