Professional Certificate in Regulatory Affairs

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Overview

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Learning outcomes

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Course content

1

Regulatory Frameworks

2

Drug Development

3

Post-Market Compliance

4

Quality Management Systems

5

Regulatory Submissions

6

Labeling and Advertising

7

Medical Devices Regulations

8

Good Manufacturing Practices

9

Regulatory Inspections

10

Clinical Trials Governance

Duration

The programme is available in two duration modes:
Fast track - 1 month
Standard mode - 2 months

Course fee

The fee for the programme is as follows:
Fast track - 1 month: GBP £140
Standard mode - 2 months: GBP £90

Career Path

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Key facts

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Why this course

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Frequently asked questions

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Specialized course covering regulations in industries like pharmaceuticals and medical devices, preparing professionals for compliance roles in regulatory affairs.

Showcase your achievement with a professional certificate upon successful course completion.