CPhI which hosts a number of successful and well respected pharmaceutical conferences in India is now launching its first workshop edition in Dubai – Proactive GCC Quality Compliance workshop taking place from 18-19 March 2015.
After a series of successful conferences in India focused on Quality Assurance and Quality Control including Computer Systems Validation, Data Integrity, Reliability and Quality Matrix and more, Proactive Quality compliance workshop in Dubai aims at examining the key local and global regulatory developments impacting GCC regulations and their evolution in 2015 and beyond.
This workshops aims at getting together 80+ quality and regulatory heads across MENA region. This highly interactive training workshop is being offered to familiarize trainees with Pharmaceutical Quality System Elements (PQSE), CAPA and practical aspects of CSV. It will provide attendees a better understanding of the elements of writing quality SOPs along with regulatory requirements for CSV. This will also provide you the required skills to keep your company compliance ready. It is specifically designed for novices, advanced users, senior management and manufacturing personnel who use computer systems for laboratories, clinical trials, biopharmaceutical manufacturing and IT system vendors engaged in the development of systems and software for the biopharmaceutical industry.
Download Brochure: http://bit.ly/1vBkQZz
For further information about the Workshop you can contact
Mr. Mustafa Nalwalla
UBM India – Conferences
T: +91 (022) 6172 7067
E: Mustafa.firstname.lastname@example.org | W: www.qualitycompliance-me.com
About Chinmoy Roy
Chinmoy Roy is an internationally recognized subject matter expert in CSV, CAPA, CFR 21 Part 11, Annex 11, Data Integrity and manufacturing process automation systems. He has been invited to speak and conduct training workshops at several international conferences such as ISPE, WBF etc. Recently he was on the panel of experts on Data Integrity along with FDA inspectors to address Data Integrity issues at ISPE’s Annual meeting which concluded in October 2014 in Las Vegas, USA. He is also a team lead in ISPE’s Data Integrity Special Interest Group (SIG). The SIG recommends industry practices for Data Integrity and the recommendations evoke interest of regulators during their audits.
Based in the US, his expertise stems from his 40 plus years of experience in validating and obtaining “fit for use” certification for over 200 IT systems. He has over 15 years’ experience at the premier world biotech company Genentech in San Francisco, California. Currently, he is a consultant at leading companies such as Roche, Genentech, Bayer, Novartis, Johnson and Johnson etc. He has authored several QA Governance documents and facilitated numerous Quality Risk Assessments. His training workshops are unique in that he blends his field experience to provide practical situations and case studies to explain the intricacies of implementing regulations. Chinmoy is a Electrical Engineering graduate from Indian Institute of Technology, Kharagpur, West Bengal and a Masters in Computer Science from Worcester Polytechnic Institute from Worcester, MA, USA.
About UBM India
UBM India is India’s leading live media and events company that engages people and enriches businesses. We at UBM India provide the industry with platforms that bring together buyers and sellers from around the world, through a portfolio of exhibitions, content led conferences & seminars, tech media, live events, data services and powerful media brands. UBM India hosts over 20 large scale exhibitions and 40 conferences across the country every year; thereby enabling trade across multiple industry verticals. A UBM Asia Company, UBM India has offices across Mumbai, New Delhi, Bangalore and Chennai. UBM Asia is owned by UBM plc which is listed on the London Stock Exchange. UBM Asia is the leading exhibition organiser in Asia and the biggest commercial organiser in mainland China, India and Malaysia.