Start dealing with full electronic submission services with regard to eCTD preparation, publishing and submission activities in Europe, US, Switzerland and GCC countries.
Medical devices are under high scrutiny – regulatory requirements are currently being reinforced, in particular to ensure patient safety (vigilance and market surveillance).
We offers full range of case processing services from collection, database entry, coding and medical assessment to regulatory submission.
We maintain a dynamic, lean, highly skilled and very creative core team of professionals who work virtually and remotely from liaison offices in Europe, USA, and Middle East.