Associate Director/Director Regulatory Affairs

The UK team of the international QbD group is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, regulatory approval, market launch, and into life cycle management. We have been offering support to life science companies for 15 years.     What do we expect from you as […]

Consultant Regulatory Affairs IVD

Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations.  Our objective is to provide manufacturers with practical solutions in the area of regulatory affairs and quality assurance. We help with the implementation of quality systems, […]

Principal Consultant Regulatory Affairs Pharma

The UK team of the international QbD group is a specialist regulatory and pharmacovigilance consultancy company. Our services consist in providing consultation throughout product development, regulatory approval, market launch, and into life cycle management. We have been offering support to life science companies for 15 years.    What do we expect from you as a […]

Regulatory Affairs Specialist – Medical Devices

At QbD our RA Services go from regulatory strategy, clinical, technical file to Vigilance. We support from idea to commercialization. Do you want to support companies throughout the entire medical device regulatory lifecycle? Do you want to guide them through complex regulatory requirements? This all in an efficient and pragmatic way? Then apply now and […]

Come visit our booth at CPHI Barcelona 2023

Come to see the QbD Group at stand #3G73 at CPHI Conference in Barcelona. And after the conference…Eat & Connect with lifescience professionals at our QbD’s CPHI Networking Drink.