Curriculum

Contract Manufacturing (CDMOs & Generics)

CDMOs and Generics play a vital role in the life sciences industry by providing essential services and products. CDMOs (Contract Development and Manufacturing Organizations) offer a range of services, including drug development, manufacturing, and testing, to pharmaceutical companies. They allow companies to outsource non-core activities, reduce costs, and accelerate time-to-market. Generics are copies of brand-name drugs that have lost patent protection. They offer lower-cost alternatives to patients and increase access to essential medications. CDMOs and Generics contribute to the overall health and well-being of populations by providing affordable and accessible medicines.

Learning Paths

Core

Build

Refresh

Good Manufacturing Practices (cGMP) - Beginner

The Devastating Effects of Not Following GMP

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Good Manufacturing Practices (cGMP) - Intermediate

Batch/Product Release

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Good Pharmacovigilance Practices (GVP)

Recalls and Consent Decrees

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FDA Inspection Readiness (GMP Auditing)

General Inspection Readiness

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Good Documentation Practices (GDocP)

CAPA and Effectiveness Checks

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Human Error Prevention

Human Error Prevention

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Contamination Control & Aseptic Techniques

Winning Cleanroom Behaviors

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Good Manufacturing Practices

In-Process Sampling and Testing

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Good Manufacturing Practices (cGMP) - Intermediate

Equipment Maintenance

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Refresher Training

Data Integrity Refresher Course

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Good Manufacturing Practices (cGMP) - Beginner

Clothing Requirements for Grades A/B, C and D

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FDA Inspection Readiness (GMP Auditing)

How Self-Inspection Leads to Continuous Improvement

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Good Manufacturing Practices (cGMP) - Beginner

The Four Main Sources of Pharmaceutical Contamination

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Good Manufacturing Practices (cGMP) - Beginner

The Importance of Contamination Control

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Good Manufacturing Practices (cGMP) - Beginner

Top 10 Principles of Good Manufacturing Practices (cGMP)

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Good Manufacturing Practices (cGMP) - Beginner

What is Drug Contamination?

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Good Manufacturing Practices (cGMP) - Beginner

What is Drug Cross Contamination?

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