Cleaning Validation in Pharmaceutical Manufacturing Facilities 4/25/2019

Cleaning validation is the process of assuring that a cleaning procedure effectively removes the residue (chemical, physical and microbiological) from manufacturing equipment/facilities below a predetermined level. Cleaning validation is primarily used for the cleaning of process manufacturing equipment. 

 

Date: April 25, 2019

 

Register:

10:00am Central European Time

11:00am Eastern Time

 

Fee: $750. Register 2 weeks in advance for Early Bird Special discount: $575.

Speaker

Gilberto Dalmaso, PhD

Global Life Science Scientific Officer

Gilberto Dalmaso has over 25 years’ experience in pharmaceutical microbiology and sterility assurance, primarily with GlaxoSmithKline (GSK).  In 2003, his laboratory gained the distinction of obtaining the world’s first rapid microbial PAT approval from the US FDA. Today Gilberto is the Global Life Science Scientific Officer for Particle Measuring Systems, serves on the European PDA Committee, is a reporter to numerous symposia on the microbiology and Pharma in Europe, Asia and United States, and is an ISO 9001 and HACCP quality system auditor.