Clinical Trial Regulations- Aurelius Corporate Solution

1
Aurelius Global Master Class
2
About Us

• WHO ARE WE?
• We find ourselves as problem solvers of the
  industry, technology and businesses for
  industrial organizations of all types and
  domains. We cover a wide array of industrial
  domains including Pharmaceutical development,
  Automotive, Transport, Oil and Gas extraction,
  Telecom, Business management, Manufacturing,
  Defense, Supply Chain Management and so on. 

• WHAT DO 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 whos who of the
  industry and have played our part in improving
  the process excellence of our customer partners

3
Hello!

• I am Roni Jennifer

4

• 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.

5
1. Clinical Trial Regulations

• With ICH GCP E6 R2 Workshop

6
MASTERCLASS OVERVIEW

• Complexity 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 organizations success.

7

• Clinical Quality Assurance should attend this
  training
• Clinical Auditing should attend this training
• Clinical Quality Pharmacovigilance should
  attend this training
• Medical Quality should attend this training
• Medical Compliance should attend this training
• R D QA should attend this training
• Clinical Research Coordinator
• Clinical CAPA should attend this training
• Clinical Quality Oversight should attend this
  training
• Clinical Data Quality should attend this training
• GCP Compliance should attend this training
• Clinical Quality Project Management should attend
  this training
• Clinical Process Management should attend this
  training
• Trail Master files should attend this training
• Clinical Research Associate should attend this
  training

WHO SHOULD ATTEND CLINICAL TRIALS TRAINING?
8
Maps

• our office
• Av Los Laureles 1090 Oficena 705,
  VitacuraSANTIAGO CHILE

9

10
Thanks!

• Any questions?
• Email masterclass.registrations_at_aurelius.in
• Website https//aureliusglobalmasterclass.com/