ABOUT NORD CONSULTING
Regulatory expertise, tailored to your project
Focused support for the preparation, assessment and maintenance of regulatory documentation for human medicinal products.
OUR PROFILE
Years of professional experience in pharmaceutical regulatory affairs
Our focus
NORD CONSULTING provides specialist regulatory affairs consulting services for human medicinal products. We support pharmaceutical businesses with regulatory dossiers, marketing authorisation procedures, compliance assessments and lifecycle activities across the United Kingdom and European Union.
Regulatory experience
With more than 15 years of professional experience in pharmaceutical regulatory affairs, our approach combines regulatory knowledge, detailed documentation review and practical support throughout the product lifecycle. This experience relates to professional work in the field and does not describe the age of the NORD CONSULTING business.
Working with clients
Projects are approached according to the medicinal product, the regulatory procedure, the available documentation and the client’s commercial or technical objectives. The scope, deliverables and responsibilities are agreed for each assignment.
Markets and products
Our core experience is in the UK, EU and wider European regulatory environment, supplemented by selected international project exposure. Support is relevant to a broad range of human medicinal products, including generic and innovative medicines, where appropriate.
DISCUSS A PROJECT
Need specialist regulatory affairs support?
Get in touch to discuss the regulatory scope and documentation requirements for your project.