Event Details: Preparing And Facing Regulatory Audits: A Practical Approach
Speaker: Maija Hietava-Lorenzi
Date & Venue:17-18 June 2010, Istanbul, Turkey
Details: The QC laboratory is essentially responsible for more than 50% of product safety and efficacy if you consider that they test raw materials, in-process materials and finished product, as well as perform stability testing, tests for process validation, cleaning validation, equipment validation and other validations and they also develop and validate analytical methods. Any company therefore relies heavily on the integrity of the data provided by its QC laboratory. This course will provide a detailed review of current regulatory requirements relating to GMPs in the laboratory as well as current industry practices.
The Workshop Leader for this event is Maija Hietava-Lorenzi, who has tremendous experience and expertise in this area. Maija used to be registered in EMEA as an EMEA Expert. She has represented the EU Commission, PQ program of WHO Geneva, and National Agency for Medicines Finland, as a Senior Pharmaceutical Inspector. She has worked in WHO PQ programme and performed GMP and GCP inspections worldwide. She has a wide experience in different positions in pharma industry and latest in biotech industry as VP - QA and Analytical Development, FIT Biotech and QP in Ark Therapeutics Oy in Finland.
for more info visit:www.pharmasupport.in
Get registration for this event visit: pharma-event-registration
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