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Fundamentals of Drug Regulatory Affairs

nisha pandya

nisha pandya

Consultant -Business Development

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Chemical & PharmaceuticalChemical & Process
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Fundamentals of Drug Regulatory Affairs

  • Trainers feedback

    ( reviews)

  • Course type

    Watch to learn anytime

  • Course duration

    25 Min

  • Course start date & time

    Access anytime

  • Language

    English

Why enroll

A career in DRA is highly rewarding due to its growing demand, high salary potential, and opportunities for career advancement. Whether through diplomas, certifications, or master's programs, gaining expertise in regulatory compliance can lead to a stable and lucrative career in the pharmaceutical industry across the U.S., Europe, India, and Australia. Regulatory affairs professionals play a key role in ensuring drug safety, efficacy, and compliance, contributing to global healthcare advancements.

Opportunities that awaits you!

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Course details

The primary objective of Drug Regulatory Affairs (DRA) is to ensure the safety, efficacy, and quality of pharmaceutical products by complying with national and international regulations. DRA professionals work to facilitate the approval, manufacturing, marketing, and distribution of drugs while adhering to regulatory guidelines set by authorities such as the FDA (USA), EMA (Europe), CDSCO (India), MHRA (UK), and WHO.

Drug Regulatory Affairs is a multidisciplinary field that bridges pharmaceutical sciences, regulatory laws, and quality compliance. It covers aspects of drug development, licensing, registration, and marketing authorization.

Course suitable for

  • Chemical & Pharmaceutical
  • Chemical & Process
  • Health, Safety & Environmental

Key topics covered

Drug regulatory affairs is a critical field focused on ensuring the safety, efficacy, and quality of pharmaceutical products.

  • Regulatory Agencies and Guidelines

  • Drug Approval Process

  • Clinical Trial Regulation

  • Market Authorization and Licensing

  • Regulatory Strategy and Lifecycle Management

Course content

The course is readily available, allowing learners to start and complete it at their own pace.

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Fundamentals of Drug Regulatory Affairs

5 Lectures

25 min

  • Lesson icon

    Overview of Drug Regulatory Affairs

    5 min

  • Lesson icon

    Career in Drug Regulatory Affairs

    5 min

  • Lesson icon

    Regulatory Affairs

    5 min

  • Lesson icon

    Drug Regulatory Affairs (DRA) Training and certification

    5 min

  • Lesson icon

    Pharmaceutical Regulatory Affairs

    5 min

Why people choose EveryEng

Industry-aligned courses, expert training, hands-on learning, recognized certifications, and job opportunities—all in a flexible and supportive environment.

nisha pandya

nisha pandya

Consultant -Business Development

Questions and Answers