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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- No Hassle Refunds
- Secure Payments
Please choose any 6 unique items from the list below to create your customized bundle and then add to cart to begin checkout.
GxP Computerised Systems
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Good Manufacturing Practice 01
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Good Manufacturing Practice 02
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GMP Refresher Training
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Good Distribution Practice
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Good Recordkeeping Practice
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Good Warehouse Practice
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10 Golden Rules of GMP
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Introduction to Practical Auditing
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Preparing for an Audit
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Remote Auditing Training
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Data Integrity
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FDA CFR 800 & CFR 820 for Medical Devices (Introduction)
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CFRs 210 & 211 for Finished Pharmaceuticals
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Release for Supply - TGA
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Supplier Qualification (GMP)
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Cleaning Validation
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Deviations and Non-Conformances
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CAPA - Corrective and Preventive Actions
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Complaints Management
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ISO 13485: Quality Management Systems for Medical Devices
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ISO 14971: Risk Management for Medical Devices
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Recalls of Therapeutic Goods
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Annex 1 - Sterile Medicinal Products
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Annex 2A ATMP Manufacturing
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Annex 2B – Manufacture of Biological Substances & Medicinal Products for Human Use
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Annex 3 - Manufacture of Radio-pharmaceuticals
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Annex 4 - Manufacture of Veterinary Medicinal Products other than Immunologicals
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Annex 5 - Manufacture of Immunological Veterinary Medicinal Products
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Annex 6 - Manufacture of Medicinal Gases
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Annex 7 - Manufacture of Herbal Medicinal Products
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Annex 8 - Sampling of Starting and Packaging Material
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Annex 9 - Manufacture of Liquids, Creams and Ointments
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Annex 10 - Manufacture of Pressurised Metered Dose Aerosol Preparations for Inhalation
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Annex 11 - Computerised Systems
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Annex 12 - Use of Ionising Radiation in the Manufacture of Medicinal Products
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Annex 13 - Manufacture of Investigational Medicinal Products
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Annex 14 - Manufacture of Products Derived from Human Blood or Plasma
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Annex 15 - Qualification and Validation
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Annex 16 - Authorised Person and Batch Release
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Annex 17 - Parametric Release
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Annex 19 - Reference and Retention Samples
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Annex 20 - Quality Risk Management ICH Q9
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