Pharma
Starting at 1:00 pm CET, we are going to be streaming exclusively for our attendees, introducing a topic with an increasing amount of attention from industry regulators and manufacturers with an emphasis on understanding the best practices for an effective and most efficient cleaning validation program. This event will provide a broad outlook and guidance on validated cleaning, including:
We are bringing you five live presentations on how to maintain and manage the cleaning program and meet regulatory requirements. Led by subject-matter experts, who will cover exciting topics that are gaining increased attention in the industry, followed up with an interactive discussion with an emphasis on understanding the best practices for an effective and efficient cleaning validation program.
Executives, Directors, Heads, Leaders, Managers, Specialists, Engineers and Fellows specializing in:
About Speaker
About Speaker
About Speaker
About Speaker
About Speaker
Andreas Schreiner graduated from the University of Erlangen, Germany, in 1996 in Chemical Engineering. After a Ph.D. and a scholarship at the University College London, he joined Roche Vitamins as Head of Solids Processing. Since 2006 Andreas Schreiner worked for Novartis in various departments with increasing responsibilities from project leader to global technology platform leader; currently, he is heading the validation activities for pharmaceutical production of solid dosage forms. Andreas Schreiner is appointed board member at various scientific organisations (Executive Board of European Federation of Chemical Engineers (EFCE), Swiss Society for Process Engineers (SGVC), Industrial Society for Pharmaceutical Engineering (ISPE), Swiss Laboratory of Material Science and Technology (EMPA)). Since 2013 he works for the Manufacturing Science & Technology Department as Validation Head for Solid Dosage Forms.
Walid El Azab is an industrial pharmacist, a qualified person and a Lean Six Sigma green belt. He is a technical services manager for STERIS Life Sciences. He provides technical support related to cleaning, disinfectants, sterility assurance and process validation. Finally, he leads audits at manufacturer sites and workshops to improve processes and inspection readiness level. Walid is a lecturer at a pharmacy and medicine university. He has published different articles and book chapters, and he is also part of working groups on sterilisation and EU GMP Annex 1 guideline revision. He is a planning committee member of the Annual PDA Conference on Pharmaceutical Microbiology (12th and 13th editions), and part of the editorial committee of the PDA Letter. Walid is an observer member of the ISPE Belgium affiliate board. Finally, he is secretary of the Belgium Qualified Person Association.
Dr. Tim Sandle has over twenty-five years of experience in microbiological research and biopharmaceutical processing. Dr. Sandle is a member of several editorials boards, and he has written over six-hundred book chapters, peer-reviewed papers, and technical articles relating to microbiology. Dr. Sandle works for a pharmaceutical manufacturer in the UK and is a visiting tutor at both the University of Manchester and UCL.
Jernej has a Master's degree in pharmaceutics. He has been in Novartis for eight years in MS&T (Manufacturing science and technology) department and has expertise in Product Validation, Packaging Validation, and Cleaning Validation.
Request the 2nd Cleaning Validation recording, and find out the latest topics and ideas that were shared during the event.
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Nov 20, 2019
3rd Annual Aseptic Processing Summit
Pharma
Pharma
Pharma
Pharma
