Training & seminars
Good Aseptic Practices And Sterile Products
5 December 2016
Where
The Boulevard St Giles Premier Hotel<br />Mid Valley City<br />Lingkaran Syed Putra,<br />59200 Kuala Lumpur, Malaysia
Aim: This subject is designed to facilitate the development of knowledge and practical skills in the assessment of special risks associated with the manufacture of sterile pharmaceuticals and to develop and evaluate strategies and plans that will ensure acceptable sterility assurance levels.
Day 1
AM ► Assess the regulatory requirements for aseptic manufacturing processes in order to provide recommendations for their application to ensure compliance
PM ► Evaluate the risks associated with aseptic processing and terminal sterilization to establish ongoing monitoring and reporting systems that can be used as the basis for changes, updates and continuous improvement.
Day 2
AM ► Critically evaluate strategies for bioburden control
PM ► Design sterilization validation protocols
Day 3
AM ► Utilize mathematical equations to evaluate, interpret and establish sterilization parameters
PM ► Perform simple tasks in an aseptic manner
Download the brochure and registration form.