Johnwick
Uploaded on Sep 25, 2019
Category
Technology
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/
Category
Technology
Biotech Products training In Europe.
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 THIS BIOTECH PRODUCTS MASTERCLASS IN
AUSTRIA?
• Process Engiineeriing Shoulld Attend Thiis Biiotech Products In house traiiniing
• Formullators Shoulld Attend Thiis biiotech Products Biiotech Products In
house traiiniing
• Technollogy Transfer Shoulld Attend Biiotech Products In house traiiniing
• Manufacturiing Management Shoulld Attend Thiis Biiotech Products In house
traiiniing
• Valliidation Speciialliists Shoulld Attend Thiis Biiotech Products In 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
• DATE & TIMEStart 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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