Learn the Computerized System Validation as per GAMP-5, 21 CFR Part 11 Guideline by Joining course

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LIMS Course is End to End learning of Laboratories Information Management Application and it's Validation efforts.

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Join Drug Regulatory Affairs Online Course to learn submission of regulatory application to various regulatory bodies, in this course you learn NDA, ANDA and various other submission. For full course join the course.

Learn Online details of Clinical Data Management System (CDMS), in this course you will learn basics of CDMS, for full course join the course by click below button. 

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Learn Online details of Pharmaceutical Quality and Validation

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Our Manufacturing Execution System (MES) Training enables you to get up to speed with the latest MES concepts and technologies.  

Candidates will learn LIVE administrative LIMS knowledge like creation and management of users, configuration of LIMS application from front end, job scheduler configuration, etc all admin level task.  

Learn Online Pharmacovigilance, in this course you will learn basics of PV, for full course join the course by click below button. 

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Learn Online details of Medical Writing, in this course you will learn basics of Medical Writing and topics to be covered, for full course join the course by click below button. 

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