Thought Leadership
At NDA our experts stay abreast with the evolving environment and the new regulatory requirements that it gives rise to. One of the results of these activities is a stream of articles, commentaries and white papers that we publish for the benefit of our clients and followers. It captures the state of the art of our industry today.
We call it Thought Leadership.
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23-09-2020
Integrated product development for ATMPs
In this article, published in the September issue of MedNous, Claes and Paula discuss why an integrated product development strategy for ATMPs is essential to meet both regulatory and HTA requirements.
02-02-2019
Design and optimisation of a quality target product profile for ATMPs
The QTPP is an inherent element of product development for an MAA, yet it is perhaps more familiar for those developing conventional pharmaceuticals
02-08-2018
CAR T-Cells for Cancer Immunotherapy – Moving Target for Industry?
This article discusses the product-and patient-related variables that may pose challenges for the industry and developers both from the scientific and regulatory perspective.
02-07-2018
How to commercialise ATMPs in the EU
This article addresses recent findings from the EMA PRIME scheme and provides information about procedural updates and evolving guidance in the ATMP area.
17-05-2018
Regulatory strategies for value maximisation of early clinical stage assets
This white paper written by Niamh Kinsella, Biologics Expert, Paul Chamberlain, Biopharmaceuticals Expert, Josi Holz, Clinical Strategy Expert and Eva Lilienberg, Service area lead Global Development, focus on how you can strengthen your partnering nego...
02-11-2017
Revamping Regulations
Safety information is required to allow clinical development of stem cell products, but clearer guidance concerning safety testing requirements is still needed.