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The IWA Consulting Team has specialized in assisting our clients from development to launch and life cycle management. We provide onsite and offsite regulatory affairs services to international private and public clients based on long term regulatory experience and in-depth knowledge, through a unique multidisciplinary approach with experts based globally. 


From Regulatory Affairs to Regulatory Science 

We have the courage to give honest advice based on our broad expertise within regulatory affairs for pharmaceutical products and medical devices.
Every consideration in your product development or maintenance has an impact on your regulatory documentation and vice versa. We have the knowledge, experience, and resource to support your project successfully, be it through providing key expert guidance, replacing a critical resource, or supporting operationally your team through critical periods of growth or change.


Our global expertise encompasses the full spectrum of health products: drugs, biologics, cell and tissue therapies, medical devices/ digital, In-Vitro Diagnostics/CDx, combination products, as well as nutraceuticals and cosmeceuticals.
For more information about the IWA Consulting Team services, from Regulatory Strategy, Agency interactions, Regulatory Project Management, eCTD Compiling and Publishing, Submission Management to Access to Market and Patients, please visit the right-hand side menu or contact us.