The IWA Consulting Team has specialized in assisting our clients from development to launch and life cycle management. We provide regulatory affairs services to a large range of international private and public clients based on long term regulatory experience and in-depth knowledge. We have the courage to give honest advice, and we have broad expertise to provide services from development to launch and life cycle management of pharmaceuticals and medical devices.
Is your organisation looking to apply for registration in the US and EU, simultaneously? The IWA Consulting Team has been through this exercise several times, and we will see your plan through to success on a global eCTD submission.
We trust that doing things right from the beginning is the fastest and most efficient route to reach the goal. Hence, we control and handle all documents from the start of a project in simple templates, which are compatible to the eCTD format. Learn more about our unique approach and IT-platform in Document Management.
For more information about the IWA Consulting Team services, please visit the right hand side menu or contact us.