Our highly experienced team provides a comprehensive set of services covering all aspects of the electronic drug regulatory affairs business. It covers electronic submission services ranging from eCTD and NeeS compilation and submission hosting to individual processing of submission documents. We also support the registration of your medicinal products in EVMPD.
In addition we provide consulting and training regarding eCTD and EVMPD and support the implementation of electronic submission and tracking systems and related processes in the global pharmaceutical industry.
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