Microbiological Best Laboratory Practices Save up to EUR 400.- by registering for Module 1 and 2! 18-20 February 2009 Amsterdam, The Netherlands Please click here to view the program of this conference or course To book for this program, just click on the option: Book this option: Module 1+2: Non-ECA Members (EUR 1980,--) Book this option: Module 1+2: ECA Members (EUR 1782,--) Book this option: Module 1+2: EU GMP Inspectorates (EUR 990,--) Book this option: APIC Members (does not include ECA Membership) (EUR 1881,--)
At this conference we offer a Conference Exhibition. Please click here in order to view the registration form (PDF) for exhibitors.
Objectives Most tests applied in microbiological QC are described in detail in the different Pharmacopoeias (e.g. EP, USP, JP). These methods are regarded as being validated – but not for your products! In the end, it is up to you to prove that the official methods function in your environment. The validation of microbiological test methods for your needs consumes a lot of time, money and manpower. Things can get more complicated if your products interfere with the execution of the test. The real challenge is to fulfil both, regulatory requirements and at the same time financial targets set by your management. During this 3-day workshop you develop strategies for a sustainable approach to the validation of microbiological test procedures. This course will give you clear guidance on how to cope with these tasks besides your routine laboratory work. The key tool of this seminar will be team work. During interactive sessions you will create procedures for the most common microbial test methods. Our experienced ECA course leaders will moderate the discussions to lead you to practice-oriented solutions. After completion of the course you will be able to cope with the validation of microbiological test procedures in a compliant and at the same time efficient manner. To guarantee optimal conditions for the exchange of opinions and experiences, the number of participants is limited! HIGHLIGHTS: - Two Modules:   Validation according to the Pharmacopoeias   The Real World - Develop testing and validation strategies in four interactive Sessions:   Sterility Testing and Total Counts   Specified Organisms   Endotoxin Testing   Environmental Monitoring - Latest Trends in Microbiological Quality Control