Uploaded on Sep 23, 2019
Biotech Products training Biotech Products Masterclass is going to happening in Austria by Aurelius global Masterclass. This for Biotech Products In house training professionals that are new to the biotechnology industry, professionals entering new work assignments encompassing biotechnology operations or individuals with previous pharmaceutical industry experience that want to learn the basics of biotechnology. for these Biotech Products Training. https://aureliusglobalmasterclass.com/events/quality-requirements-for-biotech-products/
BIOTECH PRODUCTS
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 THIIS BIIOTECH PRODUCTS MASTERCLASS IIN
AUSTRIIA?
• Process Engiineeriing Shoulld Attend Thiis Biiotech Products IIn house traiiniing
• Formullators Shoulld Attend Thiis biiotech Products Biiotech Products IIn
house traiiniing
• Technollogy Transfer Shoulld Attend Biiotech Products IIn house traiiniing
• Manufacturiing Management Shoulld Attend Thiis Biiotech Products IIn house
traiiniing
• Valliidation Speciialliists Shoulld Attend Thiis Biiotech Products IIn house traiiniing
Biotech Products training
• Learniing
o How to optimiize budget by miiniimiiziing downtime and executing
smoother Shutdown & Turnaround project
• Sollviing
o Techniicall and management iissues of Shutdown & Turnaround’s
enhanciing lliife cyclle whiille maiintaiiniing budget
• Proviidiing
o A detaiilled viiew of the turnaround management system process
and procedurall framework for both petrochemiicall pllants and
refineriies
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
• Manufacturiing of the Drug Substance and IMP
• Requiirements for processvalliidation
• IMPs comparators and placebos
• Rellease speciifications versus InProcess Controlls, ICH
guiidelliines
• Anallyticall methods throughout clliiniicall devellopment, Batch
data
• The siite master fille (SMF)
• Manufacturiing process changes duriing clliiniicall devellopment
• 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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