Uploaded on Sep 26, 2019
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/
Biotech Products training In Europe
AURELIUS GLOBAL
MASTERCLASS
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
Valliidatiion Speciialliists Shoulld Attend Thiis Biiotech Products IIn 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
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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