Course: HES6429/SP6407 Risk Management in Pharmaceutical Industry Introducing Behavioural GMPs: bGMP™ SP6431 Value Added Deviation Management SP6432 Integrated Quality Management Systems-Principles of ICH Q10 and ISO13485 SP6433 Lean, Risk Based, Value Added Validation SP6434 Analysing Quality Problems Using 6 Sigma Tools SP6435 Behavioral GMP–A New Approach to Compliance Training HES6401 International GMPs and Quality Assurance HES6402 GMP for Manufacturing Operations HES6403 Validation Principles HES6404 Good Quality Control Lab Practices HES6405 Contamination Control HES6406 Process Development for Therapeutics - Perspective for Protein Therapeutics HES6407(1) Process Development for Therapeutics-Perspective for Small Molecules HES6407(2) Process Development for Therapeutics-Finished Dose Forms HES6408 Product Development for Therapeutics-Perspective for Medical Devices HES6409 Validation Practices HES6410 Good Laboratory Practices(for Non-Clinical Laboratories) HES6411 Computer Systems Validation Principles HES6412 Computer System Validation Practices HES6413 Good Asceptic Practices and Sterile Products HES6414 Clinical Trials Quality Assurance Management HES6415 GxP and Quality Auditing Practices HES6416 Pharmaceutical Engineering - Facility, Equipment, and Process Design HES6417 Introduction to Microbiology HES6418 Chemical Analysis of Pharmaceuticals HES6423 Process Development for Therapeutics-Finished Dose Forms HES6430 Statistics for Pharmaceutical and Medical Device
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