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Clinical Trial Regulations

Clinical Trial Regulations <br>OVERVIEW<br>clinical trials have increased dramatically in recent years, evolutions in technology and risk management process offer new opportunities to increase efficiency and focus on relevant activities and clinical trial protocols.<br>TARGET INDUSTRY <br>Clinical Research Organizations, Biotech companies, Clinical Research Services Suppliers, Large to small Pharmaceutical companies, Non-Commercial Research Organizations.<br>VENUE <br>Amsterdam, The Netherlands<br>http://bit.ly/2Z59r7P

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Clinical Trial Regulations

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  1. AURELIUS GLOBAL MASTERCLASS LEARN FROM THE BEST IN THE WORLD

  2. 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.

  3. 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 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.

  4. Some Of Our Masterclass

  5. Clinical Trial Regulations Masterclass clinical trials have increased dramatically in recent years, evolutions in technology and risk management process offer new opportunities to increase efficiency and focus on relevant activities and clinical trial protocols. TARGET INDUSTRY Clinical Research Organizations, Biotech companies, Clinical Research Services Suppliers, Large to small Pharmaceutical companies, Non-Commercial Research Organizations.

  6. Clinical Development Manager should attend this clinical trials training • Clinical Operations Manager should attend this clinical trials training • Director Clinical Development should attend this clinical trials training • Director Clinical Operations should attend this clinical trials training • Head Of Clinical Operations should attend this clinical trials training • Head Of Regulatory Affairs should attend this clinical trials training • Regulatory Affairs Officer should attend this clinical trials training in Europe • Senior Manager Clinical Operations should attend this clinical trials training in Europe WHO SHOULD ATTEND CLINICAL TRIALS TRAINING?

  7. 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 KEY BENEFITS

  8. DATE & TIME Start Time 9:00 am September 17, 2019 Finish Time 5:00 pm September 18, 2019 Address Amsterdam, The Netherlands

  9. Email:masterclass.registrations@aurelius.in Phone: +44 2032 398083 Website – www.aureliusglobalmasterclass.com ANY QUARIES ?

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