Pharmaceutical Industry Seminar #11 by Huachiew Chalermprakiet University

At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of ISO 8573, in Point of Use Part 1 to be focus on the quality of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of ISO 8573, in Point of Use Part 1 to be focus on the quality of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of ISO 8573, in Point of Use Part 1 to be focus on the quality of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of ISO 8573, in Point of Use Part 1 to be focus on the quality of At this time, Atlas Copco (Thailand) Limited has opportunity to present the standard of ISO 8573, in Point of Use Part 1 to be focus on the quality of ISO 8573-1:2010 at POUs and How to monitor and minimize the contaminants at POUs (Sampling and Analysis) by Ms. Siriwan Petchutairung – Sales Engineer of Industrial Air Division.

The strength of the seminar’s objective is the promise to raise professional standards for pharmaceutical industrial in Thailand because this seminar has been in existence for 10 years and has entered its 11th year. The important key and effective to quality of medicinal products. The regulations and cGMPs require us to qualify and monitoring from start till downstream. The updated standard to control the quality of critical facilities and utility output i.e. The strength of the seminar’s objective is the promise to raise professional standards for pharmaceutical industrial in Thailand because this seminar has been in existence for 10 years and has entered its 11th year. The important key and effective to quality of medicinal products. The regulations and cGMPs require us to qualify and monitoring from start till downstream. The updated standard to control the quality of critical facilities and utility output i.e. The strength of the seminar’s objective is the promise to raise professional standards for pharmaceutical industrial in Thailand because this seminar has been in existence for 10 years and has entered its 11th year. The important key and effective to quality of medicinal products. The regulations and cGMPs require us to qualify and monitoring from start till downstream. The updated standard to control the quality of critical facilities and utility output i.e. The strength of the seminar’s objective is the promise to raise professional standards for pharmaceutical industrial in Thailand because this seminar has been in existence for 10 years and has entered its 11th year. The important key and effective to quality of medicinal products. The regulations and cGMPs require us to qualify and monitoring from start till downstream. The updated standard to control the quality of critical facilities and utility output i.e. ISO 8573 etc. some of them have been conflicted of interruption i.e. EN779, ISO 16890 etc. The topics of this seminar to updated on Thai FDA's perspective on new regulatory, new global standard and clarify to existing, understand the important of critical utilities (Compressed dry air and pharmaceutical water) to monitoring and control the quality, understanding the alternative unit approach for utilities treatment, and learn how to monitoring (sampling and analysis) and control the quality of critical utilities and POUs. The most benefit of this seminar to interaction and exchanging the experience between participant, speaker, and expert’s owner.