BIOTECH PRODUCTS TRAINING in Austria


Johnwick

Uploaded on Oct 9, 2019

Category Technology

Biotech Products Training in Austria 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, Maintenance Staff Should Attend This biotech Products Masterclass The principles of regulatory-scientific Quality assessment for these Biotech Products Training in Europe. https://aureliusglobalmasterclass.com/events/quality-requirements-for-biotech-products/

Category Technology

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BIOTECH PRODUCTS TRAINING in Austria

AURELIUS GLOBAL MASTERCLASS Biiotech Products Training in Austria 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 TRAIINIING IIN AUSTRIIA?  Process Engiineeriing Shoulld Attend Thiis Biiotech Products IIn traiiniing IIn Europe  Formullators Shoulld Attend Thiis biiotech Products Biiotech Products IIn house traiiniing  Technollogy Transfer Shoulld Attend Biiotech Products traiiniing iin Europe.  Manufacturiing Management Shoulld Attend Thiis Biiotech Products IIn house traiiniing  Valliidatiion Speciialliists Shoulld Attend Thiis Biiotech Products traiiniing iin Europe Biotech Products training in Europe  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 Biotech IMPs GMP requirements for IMPs • Manufacturing of the Drug Substance and IMP • Requirements for process validation • IMPs comparators and placebos • Release specifications versus In Process 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