Uploaded on Sep 26, 2019
Biotech Products training In Europe Biotech Products Masterclass is going to happening in Austria by Aurelius global Masterclass. This for Biotech Products In house training in Austria professionals that are new to the biotechnology industry, Regulatory landscape for national CTA procedures How the assessors in Europe work Biotech Products Training or individuals with The course will identify .the manufacture of products pharmaceutical products want to learn the basics of biotechnology. for these Biotech Products Training in Europe. https://aureliusglobalmasterclass.com/events/quality-requirements-for-biotech-products/
Biotech Products training In Europe
AURELIUS GLOBAL MASTERCLASS Biotech Products training By AURELIUS GLOBAL MASTERCLASS ABOUT US Aurelius Corporate Solutions wants to be seen and accepted as one stop shop for all industry specific master-classes across the globe, thereby making the line managers well versed with the acceptable technology and business practices, adopted worldwide. WHO ARE WE ? WHAT WE DO ? WHO SHOULD ATTEND THIIS BIIOTECH PRODUCTS MASTERCLASS IIN AUSTRIIA? Process Engiineeriing Shoulld Attend Thiis Biiotech Products IIn house traiiniing Formullators Shoulld Attend Thiis biiotech Products Biiotech Products IIn house traiiniing Technollogy Transfer Shoulld Attend Biiotech Products IIn house traiiniing Manufacturiing Management Shoulld Attend Thiis Biiotech Products IIn house traiiniing Valliidatiion Speciialliists Shoulld Attend Thiis Biiotech Products IIn house traiiniing Biotech Products training Learning o How to optimize budget by minimizing downtime and executing smoother Shutdown & Turnaround project Solving o Technical and management issues of Shutdown & Turnaround’s enhancing life cycle while maintaining budget Providing o A detailed view of the turnaround management system process and procedural framework for both petrochemical plants and refineries KEY TOPICS KEY TOPICS OF BIOTECH PRODUCTS TRAINING IN EUROPE • Regulatory framework for Clinical trials of Biotech-IMPs • The quality challenges for BiotechIMPs GMP requirements for IMPs • Manufacturing of the Drug Substance and IMP • Requirements for processvalidation • IMPs comparators and placebos • Release specifications versus InProcess Controls, ICH guidelines • Analytical methods throughout clinical development, Batch data • The site master file (SMF) • Manufacturing process changes during clinical development Start Time DATE & TIME 9:00 am 05–December , 2019, Finish Time 5:00 pm 06-December , 2019 Address Amsterdam, The Netherlands CONTACT US Email:[email protected] Phone: +44 2032 398083 Our Page :aureliusglobalmasterclass.com
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