Training Catalog
Category
Categories
Featured accredited learning paths
Combination Products
Combination Products (Drugs, Devices and Biologics) – Part 3
Combination Products
Combination Products (Drugs, Devices and Biologics) – Part 2
Combination Products
Combination Products (Drugs, Devices and Biologics) – Part 1
21 CFR Part 820
21 CFR Part 820 Subpart K: Labeling and Packaging Control
21 CFR Part 820
21 CFR Part 820 Subpart J – Corrective and Preventive Action
Good Manufacturing Practices (cGMP) - Beginner
The Devastating Effects of Not Following GMP
ISO 13485:2016
ISO 13485:2016 – Product Realization (Chapter 7 – Part B)
Good Manufacturing Practices (cGMP) - Intermediate
Good Manufacturing Practices – Good Practices and Quality Control
ISO 13485:2016
ISO 13485:2016 Product Realization (Chapter 7 – Part A)
CSV - Intermediate
Computer System Validation – Requirements: The Basis for Validation
ISO 13485:2016
ISO 13485:2016 – Chapter 5: Management Responsibility
CSV - Intermediate
Computer System Validation – The Regulated Software Life Cycle
CSV - Intermediate
Computer System Validation (CSV) – Basic Concepts, Regulations and GAMP®5
Equipment Qualification
How to Perform a Failure Mode Effect Analysis (FMEA) – Part 2
Good Documentation Practices (GDocP)
How to Manage Deviations in a GMP Environment – Part 2
Good Documentation Practices (GDocP)
How to Manage Deviations in a GMP Environment – Part 1
Contamination Control & Aseptic Techniques
Contamination Prevention and Control – Quality Risk Management (QRM)
Equipment Qualification
How to Perform a Failure Mode Effect Analysis (FMEA) – Part 1
Contamination Control & Aseptic Techniques
Sources of Contamination in a GMP Environment
Contamination Control & Aseptic Techniques
Types of Contamination in a GMP Environment
21 CFR Part 820
21 CFR Part 820 Subpart G – Production and Process Controls
FDA Inspection Readiness (GMP Auditing)
How To Be An Effective GMP Auditor – Part 3
FDA Inspection Readiness (GMP Auditing)
How to be an Effective GMP Auditor – Part 2
FDA Inspection Readiness (GMP Auditing)
How to be an Effective GMP Auditor – Part 1
21 CFR Part 820
21 CFR Part 820 Subpart F – Identification and Traceability
Good Documentation Practices (GDocP)
Good Documentation Practices – Data Integrity for General Test Results
Good Documentation Practices (GDocP)
Good Documentation Practices – Logbook Data Integrity
Good Documentation Practices (GDocP)
Good Documentation Practices – Making Correction to Ensure Data Integrity
Good Documentation Practices (GDocP)
Good Documentation Practices – General Rules of Data Integrity
21 CFR Part 820
21 CFR Part 820 Subpart B – Quality System Requirements
Good Manufacturing Practices (cGMP) - Intermediate
cGMP – Equipment, Validation, Complaints and Self Inspection
Good Manufacturing Practices (cGMP) - Intermediate
Good Manufacturing Practices – QMS, Premises and Personnel
Good Manufacturing Practices (cGMP) - Intermediate
cGMP – Cases from History and the Regulations
Good Laboratory Practices (cGLP)
Good Laboratory Practices: History and Regulatory Compliance
Good Laboratory Practices (cGLP)
How to Prepare for Internal & External Laboratory Audits
Good Laboratory Practices (cGLP)
Laboratory Investigations & Deviations
Good Laboratory Practices (cGLP)
Performing Analytical Analysis in a Regulated Laboratory
Good Laboratory Practices (cGLP)
Organization and Roles for the Regulated Laboratory
Featured Courses
Course Code
Course Name
Duration
Combination Products
MDSAP
21 CFR Part 820
Good Manufacturing Practices (cGMP) - Beginner
ISO 13485:2016
Good Manufacturing Practices (cGMP) - Intermediate
CSV - Intermediate
Equipment Qualification
Good Documentation Practices (GDocP)
Contamination Control & Aseptic Techniques
FDA Inspection Readiness (GMP Auditing)
Process Validation
21 CFR Part 11
CSV - Beginner
Good Laboratory Practices (cGLP)
