QbD Group
Francisco Javier Canut Andreu is a seasoned professional with extensive experience in the Life Sciences and healthcare sectors. Currently serving as a Project Manager and Life Science Consultant at Grupo QBD since August 2022, Francisco contributes to the qualitative development and production of products throughout their lifecycle. Prior to this, a lengthy career at Grifols, spanning from April 1993 to June 2021, included roles as a Validation Engineer, Production Team Lead, and Supervisor de turno de producción, establishing expertise in bio-pharmaceutical solutions. Francisco's educational background includes multiple advanced degrees in Business Administration and Project Management from esteemed institutions such as EAE Business School and Universitat de Girona, complemented by certifications in coaching and foreign language teaching.
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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.