Martin Schmid

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regulatory information management submission publishing lifecycle management ectd nees etc product registration planning tracking xevmpd idmp pharmacovigilance management susar icsr psur e2b meddra cioms medwatch r3 document management master data management software development document management system quality management system clinical trial management pharmacovigilance solutions idmp compliance ectd submission regulatory publishing services submission management registration management data management submission validation safety management training & education services technical consulting automation in regulatory processes compliance solutions regulatory data management quality assurance document automation workflow management business process consulting regulatory compliance safety reporting clinical document management regulatory submission templates integrated regulatory solutions risk management user training programs life sciences software regulatory agency support customer support services flexible it solutions quality control workflows automated validation regulatory process optimization document archiving solutions pharmaceutical compliance submission tracking multi-region compliance software as a service user-friendly interface back office optimization operational efficiency consultative approach innovation in life sciences data security measures information technology & services saas computer software