Curriculum

Inspection Readiness

Inspection readiness in the life sciences industry refers to the state of preparedness of an organization to undergo regulatory inspections. It involves ensuring that all operations, systems, and documentation are in compliance with relevant regulations and industry standards.

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Accredited Courses

Fundamentals Series

The Fundamentals of Inspection Readiness

15 mins
Basic

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Accredited Courses

FDA Inspection Readiness (GMP Auditing)

General Inspection Readiness

20 mins
Basic

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Accredited Courses

FDA Inspection Readiness (GMP Auditing)

Inspection Readiness: Your Role & Preparing for Inspector Interactions

25 mins
Basic

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Microlearning

FDA Inspection Readiness (GMP Auditing)

How Self-Inspection Leads to Continuous Improvement

3 mins
Basic

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Microlearning

Microlearnings

How to Act When an Inspector is On Site

2 mins
Basic

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Microlearning

FDA Inspection Readiness (GMP Auditing)

Responding to Open-Ended Questions

2 mins
Basic

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Microlearning

Microlearnings

The Difference Between Audits and Inspections

3 mins
Basic

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Microlearning

Types of GMP Inspections (PAI, Routine, For Cause)

3 mins
Basic

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Microlearning

FDA Inspection Readiness (GMP Auditing)

What Does It Mean To Be Inspection Ready?

2 mins
Basic

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Microlearning

Good Manufacturing Practices (cGMP) - Beginner

Why are Regulatory Inspections So Critical?

1 min

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