We provide project based mentoring for regulatory departments and bespoke training for your regulatory affairs team.

Training in compliance requirements related to Good Practice expectations for healthcare products is also offered for:

  • Company Executives & Board Members
  • Pharmacovigilance Officers
  • GxP for Applicants / Holders of Certificates of Registration
  • Regulatory Documents | Authoring & Editing
  • Registrations for Africa
  • Regulatory Affairs Departments:
    • Managers & Responsible Pharmacists
    • Pharmacists / Scientists
    • Assistants

Our Training Calendar for 2017 can be accessed here: 2017-TrainingCalendar_MRA_v3_2016-12-19.

Contact training@mra-regulatory.com for your training requirements / enquiries.

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