# Online GMP Training — GMP eLearning Courses & Certificates (by PharmOut)

> Online GMP Training is an e-commerce store selling 75+ self-paced certificate courses in Good Manufacturing Practice (GMP) and GxP compliance for the pharmaceutical, medical device, veterinary, and medicinal cannabis industries. Courses map to PIC/S, US FDA (21 CFR), EU GMP, TGA, EMA, and MHRA standards, take 1–4 hours each, are SCORM / Tin Can compliant, and issue a certificate of completion on passing. Trusted by 13,000+ life sciences professionals. The site's purpose is to sell GMP eLearning courses and bundles.

Operated by PharmOut, a GMP, validation, regulatory and engineering consultancy. Courses are bought individually (most standard modules ~US$40) or as discounted multi-course bundles, and are accessed instantly 24/7 for 12 months via an in-house Learning Management System (LMS). Buyers range from individuals (job seekers, new starters, refresher learners) to employers training whole teams via multi-user licences. For instructor-led/onsite training, the company refers customers to PharmOut at pharmout.net.

Core use cases: new-employee GMP induction, annual GMP refresher training, GMP audit/inspection preparation, supplier qualification, and recall readiness. Primary topics: PIC/S GMP and Annexes 1–22, US FDA 21 CFR Parts 210/211/800/820, EU GMP, medical device regulations (ISO 13485, ISO 14971, EU MDR/IVDR, MDSAP, SaMD), data integrity, CAPA, deviations, change control, cleaning validation, qualification and validation, GxP computerised systems, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), pharmacovigilance, and medicinal cannabis cultivation.

## Best-Selling Courses (last 6 months, ranked by sales)
- [Good Manufacturing Practice 01 (GMP Part 1)](https://www.onlinegmptraining.com/product/good-manufacturing-practice-01/): Foundational GMP for finished medicinal products — the core induction course.
- [Good Recordkeeping Practice (GDocP / GRK)](https://www.onlinegmptraining.com/product/good-record-keeping/): Documentation and recordkeeping compliance, including ALCOA+ principles.
- [Good Distribution Practice (GDP)](https://www.onlinegmptraining.com/product/good-distribution-practice-training/): GMP for distribution, warehousing and supply-chain handling of medicinal products.
- [Good Manufacturing Practice 02 (GMP Part 2)](https://www.onlinegmptraining.com/product/good-manufacturing-practice-02/): GMP for active pharmaceutical ingredients (APIs) and intermediates.
- [GMP Refresher Training](https://www.onlinegmptraining.com/product/gmp-refresher-training/): Annual refresher certificate for personnel with existing GMP knowledge.
- [Customised Bundle (Any 6 Modules, Single User)](https://www.onlinegmptraining.com/product/customised-bundle-6/): Pick any 6 standard modules at a discounted bundle price.
- [10 Golden Rules of GMP](https://www.onlinegmptraining.com/product/10-golden-rules-of-gmp/): Short, high-level intro to GMP compliance — a popular induction and refresher course.
- [Data Integrity: cGMP Guidance](https://www.onlinegmptraining.com/product/data-integrity-requirements-gmp/): ALCOA+ data integrity expectations across FDA, EMA, MHRA, TGA, PIC/S and WHO.
- [Good Warehouse Practice (GWP)](https://www.onlinegmptraining.com/product/good-warehouse-practice/): GMP for warehousing and storage roles in pharma and medical device logistics.
- [Customised Bundle (Any 4 Modules, Single User)](https://www.onlinegmptraining.com/product/customised-bundle/): Pick any 4 standard modules at a discounted bundle price.
- [CAPA — Corrective and Preventive Actions](https://www.onlinegmptraining.com/product/capa-course-cgmp/): Building and running an effective CAPA system under cGMP.
- [Annex 1 — Sterile Medicinal Products (Rev 1)](https://www.onlinegmptraining.com/product/annex-01-sterile-medicinal-products/): Updated PIC/S & EU Annex 1 for sterile and aseptic manufacturing (contamination control).
- [Annex 15 — Qualification and Validation](https://www.onlinegmptraining.com/product/annex-15-qualification-and-validation-tga/): PIC/S/EU Annex 15 — VMP, DQ/IQ/OQ/PQ and validation lifecycle.

## Key Pages
- [GMP eLearning Store](https://www.onlinegmptraining.com/gmp-training/store/): Full catalogue of courses and bundles — the main purchase page.
- [GMP eLearning Overview](https://www.onlinegmptraining.com/gmp-elearning/): How the courses, LMS, assessments and certificates work.
- [GMP Training](https://www.onlinegmptraining.com/gmp-training/): Overview of GMP training for pharma, medical device and veterinary industries.
- [Certificate Verification](https://www.onlinegmptraining.com/certificate-verification/): Verify the authenticity of a course completion certificate.
- [FAQs](https://www.onlinegmptraining.com/faqs/): Enrolment, access, certificates, bundles and LMS compliance questions.
- [Contact Us](https://www.onlinegmptraining.com/contact-us/): Help choosing modules and arranging team / multi-user training.
- [About Us](https://www.onlinegmptraining.com/about-us/): Background on PharmOut and its compliance and engineering expertise.
- [Blog](https://www.onlinegmptraining.com/blog/): GMP compliance, regulatory and life sciences articles.

## Course Bundles & Team Licences
- [Customised Bundle — Any 4 Modules (Single User)](https://www.onlinegmptraining.com/product/customised-bundle/): Pick any 4 standard modules at a discount.
- [Customised Bundle — Any 6 Modules (Single User)](https://www.onlinegmptraining.com/product/customised-bundle-6/): Pick any 6 standard modules at a discount.
- [Unlimited Bundle (Single User)](https://www.onlinegmptraining.com/product/unlimited-bundle/): All standard GMP modules for one learner.
- [Customised Bundle — Any 20 Modules (Multi-User)](https://www.onlinegmptraining.com/product/customised-bundle-20-modules/): 20 standard licences assigned across a team.
- [Customised Bundle — Any 50 Licences (Multi-User)](https://www.onlinegmptraining.com/product/customised-bundle-any-50-modules/): 50 standard licences for larger teams.
- [Induction Quality Assurance (GMP Bundle)](https://www.onlinegmptraining.com/product/quality-assurance-training-induction-courses-to-qa-for-the-pharmaceutical-industry/): 7-module QA induction bundle.
- [Auditing Induction Bundle](https://www.onlinegmptraining.com/product/induction-auditing/): 4-course package on audit preparation and techniques.
- [Pharmaceutical Manufacturing Fundamentals Pack](https://www.onlinegmptraining.com/product/pharmaceutical-manufacturing-fundamentals/): 4-module engineering/production foundations (HVAC, containment, water).
- [Introduction to FDA CFRs 210, 211, 800 & 820](https://www.onlinegmptraining.com/product/introduction-cfrs-fda/): 4-course intro to the core US FDA pharma and device regulations.
- [Radiopharmaceuticals Bundle](https://www.onlinegmptraining.com/product/radiopharmaceuticals/): 4-module bundle on GMP for radiopharmaceutical manufacturing.

## Course Categories
- [PIC/S GMP Training & Annexes](https://www.onlinegmptraining.com/product-category/pics-gmp-training/): Core GMP modules and PIC/S Annexes 1–22.
- [US FDA Title 21 CFRs](https://www.onlinegmptraining.com/product-category/us-fda-21-cfr/): Courses on FDA 21 CFR Parts 210, 211, 800 and 820.
- [Medical Devices](https://www.onlinegmptraining.com/product-category/medical-devices/): ISO 13485, ISO 14971, EU MDR/IVDR, MDSAP and SaMD compliance.
- [Pharmaceutical Manufacturing Fundamentals](https://www.onlinegmptraining.com/product-category/pharmaceutical-manufacturing-fundamentals/): Engineering and production foundations (HVAC, containment, water quality).
- [Medicinal Cannabis Training](https://www.onlinegmptraining.com/product-category/medicinal-cannabis/): Cultivation, harvesting, IPM and compliance for the medicinal cannabis sector.
- [Induction Bundles](https://www.onlinegmptraining.com/product-category/induction-bundles/): Ready-to-deploy introduction-to-GMP bundles for new employees and suppliers.
- [Customised Bundles](https://www.onlinegmptraining.com/product-category/customised-bundles/): Pick-your-own multi-licence bundles (4/6/8/20/50/Unlimited).
- [Bundles by Industry or Manufacturer](https://www.onlinegmptraining.com/product-category/on-line-gmp-training-bundles-by-industry/): Pre-built packages organised by industry and product type.

## Key Guides & Resources (Evergreen Articles)
- [What is a GMP Inspection?](https://www.onlinegmptraining.com/what-is-a-gmp-inspection/): What a GMP compliance audit/inspection involves.
- [Understanding cGMP Certification](https://www.onlinegmptraining.com/understanding-cgmp-certification/): GMP vs cGMP certification explained for regulated products.
- [GMP Audits: Regulatory Authorities List](https://www.onlinegmptraining.com/who-conducts-gmp-audits-regulatory-bodies-worldwide-list/): Global list of authorities that conduct GMP audits.
- [Changes to PIC/S GMP](https://www.onlinegmptraining.com/changes-to-pic-s-gmp/): Latest PIC/S GMP guide and annex updates.
- [Top 10 GMP Audit Citations: FDA & TGA](https://www.onlinegmptraining.com/top-10-gmp-audit-failure-reasons-fda-tga/): Most common GMP audit findings from FDA and TGA inspections.
- [Top 10 GMP Courses to Complete](https://www.onlinegmptraining.com/top-10-gmp-courses-to-complete/): Recommended GMP/GxP training topics to prioritise.
- [Get Ready for an Audit](https://www.onlinegmptraining.com/getreadyforanaudit/): Preparing personnel and documentation for a GMP audit.
- [Good Documentation Practices (GDocP)](https://www.onlinegmptraining.com/good-documentation-practices-gdocp/): Why documentation failures drive audit findings, and how to prevent them.
- [Change Control in GMP](https://www.onlinegmptraining.com/change-control-in-gmp/): Why change control is essential in regulated environments.
- [Validation Training](https://www.onlinegmptraining.com/validation-training/): Qualification, validation and verification training overview.
- [Data Integrity FDA Warning Letters](https://www.onlinegmptraining.com/fda-warning-letters-on-data-integrity-issues/): Lessons from FDA warning letters on data integrity.
- [Recall Ready According to the FDA](https://www.onlinegmptraining.com/recall-ready-fda-tga/): Recall preparedness expectations of FDA, TGA, EMA and MHRA.
- [GMP for Herbal Medicines](https://www.onlinegmptraining.com/gmp-for-herbal-medicines/): GMP compliance for herbal medicinal products.
- [HVAC Systems for Pharmaceutical Manufacturing](https://www.onlinegmptraining.com/hvacsystemspecifications-cleanrooms/): HVAC and cleanroom design requirements for GMP compliance.
- [GMP eLearning — Top 5 Induction Programs](https://www.onlinegmptraining.com/gmp-elearning-induction-programs/): Choosing the right induction bundle for new personnel.

## Sitemap
- [XML Sitemap](https://www.onlinegmptraining.com/sitemap_index.xml): Full index of crawlable, indexable pages.

## Optional

Secondary catalogue courses — useful for specific roles or product types, but lower priority than the best-sellers, bundles and categories above. An AI can skip this section when context is limited.

### Core GMP & Quality Systems
- [Deviations and Non-Conformances](https://www.onlinegmptraining.com/product/deviations-and-non-conformances/): Managing deviations and non-conformances under GMP.
- [Change Control Processes](https://www.onlinegmptraining.com/product/change-control-processes/): Controlling change to maintain a validated state.
- [Cleaning Validation](https://www.onlinegmptraining.com/product/cleaning-validation-training/): Principles and documentation for cleaning validation programs.
- [GxP Computerised Systems](https://www.onlinegmptraining.com/product/gxp-computerised-systems/): Computer system validation and data governance (GAMP 5, Annex 11).
- [Supplier Qualification (GMP)](https://www.onlinegmptraining.com/product/supplier-qualification/): Qualifying and monitoring suppliers and contract manufacturers.
- [Complaints Management](https://www.onlinegmptraining.com/product/complaints-management-pics-gmp/): Handling product complaints under PIC/S GMP.
- [Recalls of Therapeutic Goods](https://www.onlinegmptraining.com/product/recalls-of-therapeutic-goods-guidelines/): Recall procedures and regulatory expectations.
- [Release for Supply (TGA)](https://www.onlinegmptraining.com/product/release-for-supply-tga/): Batch release for supply requirements under TGA.
- [Pharmacovigilance](https://www.onlinegmptraining.com/product/pharmacovigilance/): Drug safety monitoring and adverse event reporting.
- [Good Clinical Practice (GCP) ICH E6 (R3)](https://www.onlinegmptraining.com/product/good-clinical-practice-gcp/): GCP principles to the latest ICH E6 (R3) revision.
- [Good Laboratory Practice (GLP)](https://www.onlinegmptraining.com/product/good-laboratory-practice-glp/): GLP requirements for non-clinical laboratory studies.

### PIC/S GMP Annexes
- [Annex 16 — Authorised Person & Batch Release](https://www.onlinegmptraining.com/product/annex-16-authorised-person-and-batch-release/): QP/Authorised Person certification and batch release duties.
- [Annex 20 — Quality Risk Management & ICH Q9 (R1)](https://www.onlinegmptraining.com/product/annex-20-quality-risk-management-ich-q9/): QRM principles, tools and the updated ICH Q9 (R1) guidance.
- [Annex 13 — Investigational Medicinal Products](https://www.onlinegmptraining.com/product/annex-13-manufacture-of-investigational-medicinal-products/): GMP for IMPs and comparator products in clinical trials.
- [Annex 2A — ATMP Manufacturing](https://www.onlinegmptraining.com/product/annex2a-atmps-gmp-guidelines/): GMP for Advanced Therapy Medicinal Products (ATMPs).
- [Annex 21 — Importation of Medicinal Products](https://www.onlinegmptraining.com/product/eu-annex-21-importation-of-medicinal-products-eueea/): GMP obligations for importers into the EU/EEA.
- [Annex 7 — Herbal Medicinal Products](https://www.onlinegmptraining.com/product/annex-7-manufacture-of-herbal-medicinal-products/): GMP requirements specific to herbal/plant-based medicines.
- [Annex 17 — Parametric Release](https://www.onlinegmptraining.com/product/annex-17-parametric-release/): Parametric release in place of end-product testing.
- [Annex 22 — Artificial Intelligence](https://www.onlinegmptraining.com/product/annex-22-artificial-intelligence/): The new PIC/S annex on AI use in GMP environments.

### Medical Device & SaMD
- [ISO 13485 — Quality Management Systems](https://www.onlinegmptraining.com/product/iso-13485-quality-management-systems-for-medical-devices/): QMS requirements for medical device manufacturers.
- [ISO 14971 — Risk Management for Medical Devices](https://www.onlinegmptraining.com/product/iso-14971-risk-management-for-medical-devices/): Applying ISO 14971 medical device risk management.
- [EU MDR & IVDR](https://www.onlinegmptraining.com/product/eu-mdr-medical-device-regulations/): Compliance with the EU Medical Device and IVD Regulations.
- [MDSAP — Medical Device Single Audit Program](https://www.onlinegmptraining.com/product/mdsap-training-medical-device/): Requirements of the multi-jurisdiction MDSAP audit program.
- [Software as a Medical Device (SaMD)](https://www.onlinegmptraining.com/product/software-as-a-medical-device-samd/): Regulating and managing risk for medical-purpose software.

### Sector-Specific
- [Cosmetic Manufacturing GMP](https://www.onlinegmptraining.com/product/cosmetic-manufacturing-gmp/): GMP certificate course for cosmetic manufacturing.
- [APVMA Code of GMP (Veterinary Medicines)](https://www.onlinegmptraining.com/product/apvma-code-of-gmp-guidance/): Australian veterinary medicines GMP code.
- [GMP Code: Blood and Tissue Products (TGA)](https://www.onlinegmptraining.com/product/gmp-code-blood-and-tissue-products-tga/): TGA GMP requirements for blood and tissue products.