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Browse our extensive catalog of GxP, Compliance & Regulatory training
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CodeCourse Name and LearnGxP.com link๐Ÿ”—Duration (minutes)Current Status Course Availability:Industry
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Annual Refresher Training
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2024 Annual Refresher Courses |An 8-part Interactive SeriesPharma & Biotech
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ELM-944Good Manufacturing Practice6Pharma & Biotech
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ELM-945Good Clinical Practice4Pharma & Biotech
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ELM-946Good Laboratory Practice3Pharma & Biotech
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ELM-947Good Pharmacovigilance Practice6Pharma & Biotech
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ELM-948Good Distribution Practice6Live| March 2024 ReleasePharma & Biotech
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ELM-949GxP Hot Topics: Cybersecurity6Pharma & Biotech
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ELM-950Good Documentation Practice4Pharma & Biotech
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ELM-951Data Integrity Refresher Course4Pharma & Biotech
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ELM-931Annual GxP Refresher Training (2023)15Live | July 2023 ReleasePharma & Biotech
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The Fundamentals of GxP Series
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๐ŸŒELM-219The Fundamentals of Good Manufacturing Practices (cGMP)13Live| March 2024 Redesign โญPharma
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๐ŸŒELM-220The Fundamentals of Good Documentation Practices (GDP/GDocP)15LiveLive
Pharma & Med Tech
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๐ŸŒELM-221The Fundamentals of Data Integrity10Live| March 2024 Redesign โญ
Pharma & Med Tech
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๐ŸŒELM-222The Fundamentals of Contamination Control15LiveLive
Pharma & Med Tech
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๐ŸŒELM-223The Fundamentals of Good Laboratory Practices 15LiveLivePharma
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๐ŸŒELM-224The Fundamentals of GxP in a Regulated Environment - Pharma15LiveLivePharma
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๐ŸŒELM-226The Fundamentals of Corrective and Preventive Actions (CAPA)15LiveLive
Pharma & Med Tech
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๐ŸŒELM-227The Fundamentals of Deviations 15LiveLive
Pharma & Med Tech
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๐ŸŒELM-228The Fundamentals of Inspection Readiness15LiveLive
Pharma & Med Tech
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๐ŸŒELM-229The Fundamentals of Quality Control (QC) 15LiveLive
Pharma & Med Tech
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๐ŸŒELM-230The Fundamentals of Computer System Validation (CSV)15LiveLive
Pharma & Med Tech
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ELM-232a
The Fundamentals of Quality Risk Management (QRM)20LiveLivePharma
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ELM-232b
Quality Risk Management (QRM): Global Regulations and Their Impact20LiveLivePharma
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ELM-247The Fundamentals of Change Control15Live| August 2023 New Release
Pharma & Med Tech
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๐ŸŒELM-926The Fundamentals of Good Clinical Practices (as of ICH E6 R2)20LiveLivePharma
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ELM-937The Fundamentals of Good Clinical Practices (as of ICH E6 R3)-In Development2024 |When R3 LivePharma
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TBDThe Fundamentals of Good Distribution Practices (GDP)-
Tech Writing Not Started
TBD
Pharma & Med Tech
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TBDThe Fundamentals of Pharmacovigilance (GVP)-
Tech Writing Not Started
TBDPharma
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ELM-255The Fundamentals of Software Testing in a Regulated Environment -
Tech Writing Complete
TBD
Pharma & Med Tech
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ELM-930The Fundamentals of Inspection Readiness for GCP-
Tech Writing Complete
2024Pharma
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ELM-195Computer Software Assurance (CSA)14Live| January 2024 New Release
Pharma & Med Tech
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ELM-723The Fundamentals of Sterile Manufacturing-
Tech Writing Complete
2024Pharma
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ELM-725The Fundamentals of Cell and Gene Therapy 15Live| August 2023 New ReleaseBiotech
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ELM-726The Fundamentals of Biotech Manufacturing11Live| January 2024 New ReleaseBiotech
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International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
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ELM-233ICH Q10 โ€“ Management Responsibilities20Live| January 2024 New ReleasePharma
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ELM-236ICH Q10 โ€“ Pharmaceutical Quality Systems-In Development SoonQ1 2024Pharma
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ELM-237ICH Q9 - Quality Risk Management20Live| August 2023 New ReleasePharma
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ELM-238ICH Q9 - Risk Management Methods and Tools20Live| October 2023 New ReleasePharma
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ELM-239ICH Q9 - QRM as Part of Integrated Quality Management20Live| December 2023 New ReleasePharma
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ELM-243ICH Q8 - Pharmaceutical Development-
Tech Writing Complete
TBDPharma
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ELM-246ICH Q7 - GMP for API (Part 1): Quality Management -
Tech Writing Complete
TBDPharma
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ELM-251ICH Q7 - GMP for API (Part 2): Operational Areas and Equipment-
Tech Writing Complete
TBDPharma
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ELM-252ICH Q7 - GMP for API (Part 3): Production Process-
Tech Writing Complete
TBDPharma
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ELM-253ICH Q7 - GMP for API (Part 4): Special Cases-
Tech Writing In Progress
TBDPharma
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21 CFR Part 11
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ELM-11221 CFR Part 11 - An Introduction 45LiveLive
Pharma & Med Tech
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ELM-11421 CFR Part 11 - Electronic Records45LiveLive
Pharma & Med Tech
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ELM-11521 CFR Part 11 - Electronic Signatures45LiveLive
Pharma & Med Tech
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ELM-11621 CFR Part 11 - Guidance30LiveLive
Pharma & Med Tech
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21 CFR Part 820
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ELM-30121 CFR Part 820 Subpart A - General Provisions30LiveLiveMed Tech
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ELM-30221 CFR Part 820 Subpart B - Quality System Requirements30LiveLiveMed Tech
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ELM-30321 CFR Part 820 Subpart C - Design Controls30LiveLiveMed Tech
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ELM-30421 CFR Part 820 Subpart D - Document Controls30LiveLiveMed Tech
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ELM-30521 CFR Part 820 Subpart E - Purchasing Controls30LiveLiveMed Tech
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ELM-30621 CFR Part 820 Subpart F - Identification and Traceability30LiveLiveMed Tech
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ELM-30721 CFR Part 820 Subpart G - Production and Process Controls30LiveLiveMed Tech
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ELM-30821 CFR Part 820 Subpart H - Acceptance Activities30LiveLiveMed Tech
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ELM-30921 CFR Part 820 Subpart I - Nonconforming Products30LiveLiveMed Tech
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ELM-31021 CFR Part 820 Subpart J - Corrective and Preventative Action 30LiveLiveMed Tech
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ELM-31121 CFR Part 820 Subpart K - Labeling and Packaging Controls30LiveLiveMed Tech
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ELM-31221 CFR Part 820 Subpart L - Handling, Storage, Distribution, and Installation30LiveLiveMed Tech
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ELM-31321 CFR Part 820 Subpart M - Records30LiveLiveMed Tech
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ELM-31421 CFR Part 820 Subpart N - Servicing30LiveLiveMed Tech
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ELM-31521 CFR Part 820 Subpart O - Statistical Techniques30LiveLiveMed Tech
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TBDAn Introduction to 21 CFR Part 820-
Tech Writing Not Started
TBDMed Tech
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Good Manufacturing Practices (cGMP) - Beginners
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ELM-710The Devastating Effects of Not Following GMP15Live (Redesign Available Q4 2024)
Pharma & Med Tech
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Good Manufacturing Practices (cGMP) - Intermediate
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ELM-201cGMP Cases From History and the Regulations30LiveLivePharma
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ELM-202cGMP QMS, Premises & Personnel30LiveLivePharma
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ELM-203cGMP Equipment, Validation, Complaints & Self-Inspection30LiveLivePharma
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ELM-204cGMP Good Practices and Quality Control30LiveLivePharma
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Good Manufacturing Practices (cGMP) - 21 CFR Part 211
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ELM-21121 CFR Part 211 Subpart B โ€“ Organization and Personnel 30LiveLivePharma
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ELM-20521 CFR Part 211 Subpart C - Buildings and Facilities 30SaLivePharma
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ELM-21221 CFR Part 211 Subpart D - Equipment 30LiveLivePharma
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ELM-20621 CFR Part 211 Subpart E - Control of Components and Drug Product Containers and Closures30LiveLivePharma
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ELM-20821 CFR Part 211 Subpart F - Production and Process Controls30LiveLivePharma
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ELM-20921 CFR Part 211 Subpart G: Packaging and Labeling Control30LiveLivePharma
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ELM-20721 CFR Part 211 Subpart H - Holding and Distribution30LiveLivePharma
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ELM-21021 CFR Part 211 Subpart J - Records and Reports30LiveLivePharma
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ELM-21321 CFR Part 211 Subpart K - Returned and Salvaged Drug Products30LiveLivePharma
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Good Manufacturing Practices (cGMP) - Eudralex Volume 4
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ELM-260Eudralex Volume 4 GMP - Introduction30
Tech Writing Complete
TBDPharma
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TBDEudralex Volume 4 GMP โ€“ Chapters 1 to 330
Tech Writing In Progress
TBDPharma
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TBDEudralex Volume 4 GMP โ€“ Chapters 4 to 630
Tech Writing In Progress
TBDPharma
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TBDEudralex Volume 4 GMP โ€“ Chapters 7 to 930
Tech Writing In Progress
TBDPharma