Working at Quality by Design:
Great rules, great pharma. And medical devices, ATMPs and cosmetics, of course. As a regulatory affairs expert you master and manage everything from strategy to approval right down to aftercare. Regardless of whether our clients are launching in Europe or beyond, rules and guidelines help safeguard the quality of the end product. And together with QbD you ensure their implementation.
– Isabel Helena de Brito Manique, pharmaceutical consultant and regulatory affairs specialist at QbD
Not what you were looking for?
Then be sure to check out our other areas of expertise.
Quality and coincidence? The two don’t mix. That’s why QbD safeguards quality for its clients. From the initial idea to the end product, from documentation to materials and much more.
Validation & qualification
No checks, no quality, right? Here, too, QbD experts offer a solution across the board and from start to finish through validation & qualification. From products tot processes, from data to software.
Project management & support
Introducing new products in the market. Launching technologies and processes. QbD project managers keep everything running smoothly for so many more projects than we could fit in this field.
Also known as Advanced Therapy Medicinal Products or cell therapy, this is an emerging market that still has some growing pains. In conjunction with Antleron, QbD intends to tackle them through a robust and automated approach.