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Professional Expert Course Records and Regulatory Affairs

Professional Expert Course Records and Regulatory Affairs

Upskilling is a better roadmap to success. Enroll in this course to learn critical principles of Biopharmaceuticals through real-life case studies & examples

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Course Highlights

  • Each student will have access through the Virtual Campus, to all relevant documentation to the areas scheduled

  • CESIF provides career assistance after satisfactory completion of their training period

  • Course content is available in all languages

Duration: 180 Days

Mode of learning: Online Classroom

Course Overview

Who should do this course ?
  • The Professional Expert Course Records and Regulatory Affairs is aimed at graduates and university graduates in the area of ??Health Sciences and Allied Workers (Pharmacy, Chemistry, Biology, etc.)

  • Students coming to their qualifications, as well as professionals recently joined the pharmaceutical industry interested in acquiring a specialization that allows them to implement their professional activity in that sector

What are the course deliverables ?
  • The objective of Professional Expert Course Records and Regulatory Affairs It is to provide students with a comprehensive, deep and practical insight into all aspects of the rules governing the registration of medicines, both nationally and internationally as well as all the necessary technical requirements for the marketing authorization of the products with all health and in the shortest time possible

More about this course
  • Course of Professional Expert in Drug Registration and Regulatory Affairs is designed to fully develop the professional skills of students in all areas of specialization theoretical and related departments Records / Regulatory Affairs of pharmaceutical companies worldwide practices

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Curriculum

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