Customized GMP Bundle 6 Modules

Customised Bundle (Any 6 Modules, Single User)

USD $180.00

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

Please choose 6 courses from the Bundled Products tab below and add to cart to begin checkout.

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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: cGMP Guidance
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FDA-CFRs-210-211-CFR-presentation
FDA Title 21 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 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
MDSAP Training - Medical Device Single Audit Program
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Annex 1 - Sterile Medicinal Products (Rev 1. Updates)
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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Annex11-computerisedsystems (PIC/S Annex 11)
Annex 11 - Computerised Systems
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Annex12-Ionisingradiation-trainingpresentation
Annex 12 - Use of Ionising Radiation in 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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PICS 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 & IVDR: 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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Change-Control-Processes
Change Control Processes
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