Customised Bundle (Any 6 Modules, Single User)

USD $150.00

Any 6 standard GMP training modules for US $150. Modules are assigned automatically to a single user at time of purchase.

Course duration: Allow from 8 to 10 hours to complete all 6 modules in your custom training bundle.*

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Description

Any 6 standard GMP training modules for US $150.

Please choose any 6 modules from the list below, add them to your cart and checkout (for this bundle, modules can only be assigned to one user).

If you are interested in bulk GMP training for multiple employees, consider the 20-module GMP eLearning bundle which allows you to choose and then assign certain modules to various employees or contractors.

Note: Courses in the categories of Pharmaceutical Manufacturing Fundamentals PMF101-104), Medicinal Cannabis Academy (MCCA101-113), Clinical Trials, SaMD, GLP and Pharmacovigilance categories are not included in the custom training course bundles.

Standard GMP Compliance Training Courses – Online

To view more details about the standard GMP training modules before purchasing, click here.

Course duration

*Our online GMP training courses vary in duration.

  • For each standard GMP or GxP online training course, allow an average of 1 hour to 2.5 hours (depending on the topics selected).
  • Example: allow 8 hours to 10 hours to complete all 6 modules in a custom 6-GMP training module bundle.
Please choose any 6 unique items from the list below to create your customized bundle and then add to cart to begin checkout.
GAMP5 Requirements - GxP computerised-systems PICS FDA CFRs Title 21 Data
GxP Computerised Systems
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PICS GMP training courses Good Manufacturing Practice Part I
Good Manufacturing Practice 01
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Good Manufacturing Practice PICS GMP Part 2
Good Manufacturing Practice 02
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gmp-refresher-course-training-onlinegmp
GMP Refresher Training
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good distribution practice (GDP) training course certificate
Good Distribution Practice
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good-record-keeping-practice-grk-alcoa-1course
Good Recordkeeping Practice
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good warehouse practice certificate course GWP education
Good Warehouse Practice
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Good Manufacturing Practice (GMP Part 1) PICS
10 Golden Rules of GMP
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Auditing-training-GMP-audit-checklist
Introduction to Practical Auditing
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Preparing for an Audit training course certificate training Auditors and auditees
Preparing for an Audit
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remote-auditing-inspectionGMP
Remote Auditing Techniques & Training
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data integrity requirements GMP
Data Integrity
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FDA-CFRs-210-211-CFR-presentation
FDA CFRs Part 210 and Part 211 for Finished Pharmaceuticals
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US FDA CFRs CFR Part 800 and CFR Part 820
FDA CFR Part 800 & Part 820 for Medical Devices
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release-for-supply-tga
Release for Supply - TGA
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Supplier Qualification program requirements file documentation
Supplier Qualification (GMP)
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Cleaning Validation GMP Course - training Cleaning Validation course
Cleaning Validation
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management of deviations-and-non-conformances
Deviations and Non-Conformances
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CAPA-training-cGMP-CAPA-course.
CAPA - Corrective and Preventive Actions
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Complaints-management-PICS-cGMP-regulations-ISO
Complaints Management
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Product recalls TGA FDA EMA MHRA
Recalls of Therapeutic Goods
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Falsified-Medicines-Prevention-GMP-elearning
Prevention of Falsified Medicinal Products
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ISO-13485-QMS-standardsmedical-device-.
ISO 13485:2016 Training - Quality Management Systems for Medical Devices
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ISO 14971 Risk Management Medical Devices Application
ISO 14971: Risk Management for Medical Devices
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MDSAP Training - Medical Device Single Audit Program
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Annex 1 - Sterile Medicinal Products (Rev 1. Updates)
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annex2a-atmps-gmp-guidelines
Annex 2A ATMP Manufacturing
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Annex 2 Manufacture of Biological Medicinal Products for Human Use
Annex 2B – Manufacture of Biological Substances & Medicinal Products for Human Use
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Annex 3 Manufacture of Radiopharmaceuticals
Annex 3 - Manufacture of Radio-pharmaceuticals
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pics-Annex-4-Veterinary-Medicinal-Products-gmp
Annex 4 - Manufacture of Veterinary Medicinal Products other than Immunologicals
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Annex-5-Immunological-Veterinary-Medicinal-Products-GMP
Annex 5 - Manufacture of Immunological Veterinary Medicinal Products
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Annex 6 Manufacture of Medicinal Gases
Annex 6 - Manufacture of Medicinal Gases
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Annex 7 - Manufacture of Herbal Medicinal Products
Annex 7 - Manufacture of Herbal Medicinal Products
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Annex 8 Sampling of Starting and Packaging Material
Annex 8 - Sampling of Starting and Packaging Material
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Annex 9 Manufacture of Liquids, Creams and Ointments
Annex 9 - Manufacture of Liquids, Creams and Ointments
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Annex 10 Manufacture of Pressurised Metered Dose Aerosol Preparations for Inhalation
Annex 10 - Manufacture of Pressurised Metered Dose Aerosol Preparations for Inhalation
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PICS Annex 11 Computerised Systems validation training course
Annex 11 - Computerised Systems
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Annex12-ionising-radiation-GMP-eLearning
Annex 12 - Use of Ionising Radiation in the Manufacture of Medicinal Products
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PICS-Annex-13-Investigational-Medicinal-Products-IMPs-V16
Annex 13 - Manufacture of Investigational Medicinal Products
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Annex 14 Manufacture of Products Derived from Human Blood or Plasma
Annex 14 - Manufacture of Products Derived from Human Blood or Plasma
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Annex 15 Qualification and Validation
Annex 15 - Qualification and Validation
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PIC/S Annex 16 GUIDELINES batch release authorised person
Annex 16 - Authorised Person and Batch Release
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Annex 17 Parametric Release
Annex 17 - Parametric Release
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Annex 19 Reference and Retention Samples
Annex 19 - Reference and Retention Samples
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Annex 20 Quality Risk Management ICH Q9
Annex 20 - Quality Risk Management & ICH Q9 (R1)
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ANNEX21-EU-Annex-21
EU Annex 21: Importation of Medicinal Products
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EUMDR-medicaldeviceregulation-download
EU MDR: Medical Device Regulations
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APVMA-Code-of-GMP guidelines
APVMA Code of GMP (Veterinary Medicines)
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TGA GMP Code for Blood & Tissue Products - Australia-GMP-Code-blood-and-tissue-product-regulations
GMP Code: Blood and Tissue Products (TGA Regulations)
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