Uploaded on Oct 3, 2019
Biotech Products Training 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, Production Management Should Attend This biotech Products Masterclass, . The principles of regulatory-scientific Quality assessment for these Biotech Products Training . • Quality Assurance Personnel Should Attend This biotech Products training.. https://aureliusglobalmasterclass.com/events/quality-requirements-for-biotech-products/
BIOTECH PRODUCTS TRAINING
AURELIUS GLOBAL
MASTERCLASS
B I O T E C H P R O D U C T S
T R A I N I N G I N A U S T R I A B Y
AURELIIUS 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 TRAINING IN
AUSTRIA?
Process Engiineeriing Shoulld Attend Thiis Biiotech Products In traiiniing In
Europe
Formullators Shoulld Attend Thiis biiotech Products Biiotech Products In
house traiiniing
Technollogy Transffer Shoulld Attend Biiotech Products traiiniing iin Europe..
Manuffacturiing Management Shoulld Attend Thiis Biiotech Products In house
traiiniing
Valliidatiion Speciialliists Shoulld Attend Thiis Biiotech Products traiiniing iin
Europe
Biotech Products in house 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 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 cllinicall devellopment
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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