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Biotech Products In- House Training

Biotech Products In- House Training <br>Biotech Products Masterclass is going to happening in Austria by Aurelius global Masterclass.<br>This for Biotech Products In house- training in Austria professionals that are new to the biotechnology industry, Release specifications versus In Process Controls, ICH guidelines basics of biotechnology. for these Biotech Products Training in Europe.<br><br>https://aureliusglobalmasterclass.com/events/quality-requirements-for-biotech-products/<br>

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Biotech Products In- House Training

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  1. AURELIUS GLOBAL MASTERCLASS Biotech Products in house training ByAURELIUS GLOBAL MASTERCLASS

  2. 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. ABOUT US

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

  4. 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 Biotech Products in house training

  5. 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 KEY TOPICS

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

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

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