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Biotech Products Training in Europe

Biotech Products Training in Europe<br>Biotech Products Masterclass is going to happening in Austria by Aurelius global Masterclass. <br><br>This for Biotech Products In house- training in Austria professionals that are new to the biotechnology industryProject Management Should Attend This biotech Products Masterclass The principles of regulatory-scientific Quality assessment for these Biotech Products Training in Europe.<br><br>t<br>https://aureliusglobalmasterclass.com/events/quality-requirements-for-biotech-products/<br>

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Biotech Products Training in Europe

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  1. AURELIUS GLOBAL MASTERCLASS Biotech Products Training in Europe ByAURELIUS GLOBAL MASTERCLASS

  2. 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.

  3. WHO ARE WE ?WHAT WE DO ? • WHO SHOULD ATTEND THIS BIOTECH PRODUCTS TRAINING IN AUSTRIA? • Process Engineering Should Attend This Biotech Products In training In Europe • Formulators Should Attend This biotech Products Biotech Products In house training • Technology Transfer Should Attend Biotech Products training in Europe. • Manufacturing Management Should Attend This Biotech Products In house training • Validation Specialists Should Attend This Biotech Products training in Europe

  4. Biotech Products training in Europe • Learningo How to optimize budget by minimizing downtime and executing smoother Shutdown & Turnaround project • Solvingo Technical and management issues of Shutdown & Turnaround’s enhancing life cycle while maintaining budget • Providingo A detailed view of the turnaround management system process and procedural framework for both petrochemical plants and refineries

  5. 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

  6. DATE & TIME • Start Time • 9:00 am • 05–December • , 2019,  • Finish Time • 5:00 pm • 06-December • , 2019 • Address • Amsterdam, The Netherlands

  7. CONTACT US Email:masterclass.registrations@aurelius.in Phone:+44 2032 398083 Our Page :aureliusglobalmasterclass.com

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