PPT 21
                     AURELIUS 
GLOBAL 
MASTERCLASS
LEARN FROM THE BEST IN THE 
WORLD
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.
What We Do
We, the pioneers in the industry, owing to our 
reach are able to influence the best minds to 
help you improve your process specifications. We 
have been associated with the who’s who of the 
industry and have played our part in improving 
the process excellence of our customer partners. 
We have helped them improve their system 
methodology by trying to inculcate the best 
industry practices by providing deep insight and 
practicality in processes and in turn help them 
improve their process systems at large.
Our speakers are among the best in the industry 
with hands on experience of the real time 
working environment
CLINICAL TRIAL 
REGULATIONS TRAININ
CGomplexity and cost of clinical 
trials have increased dramatically 
in recent years. Learn how 
evolutions in technology and risk 
management process offer new 
opportunities to increase 
efficiency and focus on relevant 
activities and clinical trial 
protocols. Understand how the 
new guidelines and regulations 
allow clinical trial research taking 
strategic decisions that benefit 
your organization’s success.
KEY BENEFITS
Learn the practical implications and phases of 
clinical trials of the new regulatory requirements 
for clinical trials, including ICH E6(R2) and the EU 
Clinical Trials Regulation in this training
Be able to implement more efficient, risk 
proportionate approaches for clinical trial 
application while continuing to ensure human 
subject protection and data integrity in this 
training
Learn to analyze risks in clinical trials and implement 
risk mitigation plans including monitoring plans in 
this training
Demonstrate sponsor oversight in line with 
regulatory requirements and Regulatory Agency 
expectations in this training
DATE & TIME
Start Time
9:00 am
September 17, 2019
Finish Time
5:00 pm
September 18, 2019
Address
Amsterdam, The Netherlands
ANY QUESTIONS ?
Email Us:  
[email protected]
Phone:  +44 2032 398083