Customised Bundle (Any 4 Modules, Single User)
USD $100.00
Any 4 standard GMP training modules for US $100. Modules are assigned automatically to a single user at time of purchase.
Course duration: Allow from 5 to 8 hours to complete all 4 modules in your custom training bundle.*
- Satisfaction Guaranteed
- No Hassle Refunds
- Secure Payments
Please choose any 4 unique items from the list below to create your customized bundle and then add to cart to begin checkout.
GxP Computerised Systems
-
+
Good Manufacturing Practice 01
-
+
Good Manufacturing Practice 02
-
+
10 Golden Rules of GMP
-
+
GMP Refresher Training
-
+
Good Distribution Practice
-
+
Good Recordkeeping Practice
-
+
Good Warehouse Practice
-
+
Introduction to Practical Auditing
-
+
Preparing for an Audit
-
+
Remote Auditing Training
-
+
Data Integrity
-
+
Release for Supply - TGA
-
+
Supplier Qualification (GMP)
-
+
FDA CFR 800 & CFR 820 for Medical Devices (Introduction)
-
+
CFRs 210 & 211 for Finished Pharmaceuticals
-
+
Cleaning Validation
-
+
Deviations and Non-Conformances
-
+
Complaints Management
-
+
CAPA - Corrective and Preventive Actions
-
+
ISO 13485:2016 Training - Quality Management Systems for Medical Devices
-
+
ISO 14971: Risk Management for Medical Devices
-
+
MDSAP Training - Medical Device Single Audit Program
-
+
Recalls of Therapeutic Goods
-
+
Annex 1 - Sterile Medicinal Products
-
+
Annex 2A ATMP Manufacturing
-
+
Annex 2B – Manufacture of Biological Substances & Medicinal Products for Human Use
-
+
Annex 3 - Manufacture of Radio-pharmaceuticals
-
+
Annex 4 - Manufacture of Veterinary Medicinal Products other than Immunologicals
-
+
Annex 5 - Manufacture of Immunological Veterinary Medicinal Products
-
+
Annex 6 - Manufacture of Medicinal Gases
-
+
Annex 7 - Manufacture of Herbal Medicinal Products
-
+
Annex 8 - Sampling of Starting and Packaging Material
-
+
Annex 9 - Manufacture of Liquids, Creams and Ointments
-
+
Annex 10 - Manufacture of Pressurised Metered Dose Aerosol Preparations for Inhalation
-
+
Annex 11 - Computerised Systems
-
+
Annex 12 - Use of Ionising Radiation in the Manufacture of Medicinal Products
-
+
Annex 13 - Manufacture of Investigational Medicinal Products
-
+
Annex 14 - Manufacture of Products Derived from Human Blood or Plasma
-
+
Annex 15 - Qualification and Validation
-
+
Annex 16 - Authorised Person and Batch Release
-
+
Annex 17 - Parametric Release
-
+
Annex 19 - Reference and Retention Samples
-
+
Annex 20 - Quality Risk Management ICH Q9
-
+
