Regulatory Affairs (RA) Training Program Cover Image
15

Jun

Regulatory Affairs (RA) Training Program

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There are no going users.
Start date 06/15/26 - 06:30
End date 07/08/26 - 07:30
  • Description

    REGULATORY AFFAIRS (RA) TRAINING PROGRAM

    Limited Period Offer – Registration Only ₹99 for First 10 Students!

    Regulatory Affairs professionals play a critical role in ensuring pharmaceutical products comply with national and international regulations. This training program is designed for life science graduates who want to build a rewarding career in the pharmaceutical industry.

    Course Modules:
    ✅ Introduction to Regulatory Affairs
    ✅ Pharmaceutical Product Lifecycle
    ✅ Drug Development Process
    ✅ CTD & eCTD Submissions
    ✅ USFDA Guidelines
    ✅ EMA Regulations
    ✅ CDSCO Regulatory Framework
    ✅ ANDA & NDA Overview
    ✅ Regulatory Documentation
    ✅ Labeling Requirements
    ✅ Post Marketing Surveillance
    ✅ Industry Case Studies

    Program Benefits:
    ✅ Industry Expert Trainers
    ✅ Practical Exposure
    ✅ Live Case Studies
    ✅ Resume Building Assistance
    ✅ Interview Preparation Sessions
    ✅ Placement Assistance Support

    Career Opportunities:
    Regulatory Affairs Associate, Regulatory Executive, Submission Specialist, Regulatory Coordinator and Compliance Specialist.

    Contact: 9019974004
    support@mercurymentors.com

    Limited Seats Available. Register Today!