General Activities: Performs submission according to local regulations. Keeps track of the progress of the approvals of the different requests made to the Ministries of Health. Implements regulatory processes, in a manner that avoids warnings or rejections of submission including those required to obtain protocol, site, marketing, and importation /exportation approval. Provides training to Clinical Operations personnel in regulatory matters in order to promote compliance with all applicable regulations. Monitor all Regulations in the region to maintain systems in compliance.
MMATISS offers a wide range of professional development opportunities. If you are an outstanding professional and you’re interested in joining our team, do not hesitate to send your resume to the address described below.
Contact MMATISS:
[email protected]
