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CTS

10th Annual Clinical Trials Summit 2019

Mumbai, India
28 May 2019
The conference ended on 28 May 2019

Important Dates

Abstract Acceptance Notification
19th March 2019
Final Abstract / Full Paper Deadline
20th March 2019
Early Bird Deadline
8th April 2019
Abstract Submission Deadline
19th May 2019

About CTS

10th Annual Clinical Trials Summit 2019 is inspiring keynote presentations, plenary talks and panel discussions. This will discuss most recent techniques, developments, novel strategies and various disciplines involved in drug discovery, clinical research, patient centricity, clinical site & supply management, medical imaging, data management and outsourcing in clinical trials. CONFERENCE REGISTRATION PROCESS: E-mail – kavitha@virtueinsight.co.in Tel: +9144 24762472 • Early Bird Discount Price (Valid Till 08th April 2019) – 1 Delegate – (INR 10,000 + GST (18%) per delegate) • Standard Price (09th April 2019 Onwards) – 1 Delegate – (INR 15,000 + GST (18%) per delegate)

Topics

Clinical research & development, Clinical data management, Clinical research services, Clinical it, Medical affairs

Call for Papers

10th Annual Clinical Trials Summit 2019 is inspiring keynote presentations, plenary talks and panel discussions. This will discuss most recent techniques, developments, novel strategies and various disciplines involved in drug discovery, clinical research, patient centricity, clinical site & supply management, medical imaging, data management and outsourcing in clinical trials. It will educate healthcare and clinical researcher professionals about design, operation, organizing, research computing, regulatory aspects and reporting of clinical trials. 

KEY THEMES DISCUSSED:-

  • Accomplish effective patient recruitment and retention in clinical trials by impacting innovations & digitisation in clinical research
  • Bettering the grade of the international health clinical research
  • Strategies for globalization in clinical trials
  • Connecting the developed and the developing nations
  • Leveraging new technologies to improve clinical trials efficiency in Asia
  • Transforming your trials procedure by implementing artificial intelligence
  • Investigating how trial sponsors and service providers can cooperate to better carry out the trial timelines while sustaining quality
  • Why pharma and biotech industries are specified for new and smarter ways to conduct clinical research
  • Operative patient recruitment and retention in clinical trials
  • What will persuade and impact the patient?
  • Successfully operate challenges in early phase clinical development
  • Overcoming the key challenges within early phase clinical trials
  • Developing risk-based monitoring implementation: Deduction in technology, Role progress and Business process
  • Concentrating on the lessons learned and best practices resulting from 5 years of RBM implementation
  • Clinical trial – A regulated procedure and plan of action
  • Data safety and efficacy of the newly developed drug. What are the mandatory for further approval of the drug to bring it into the market
  • Understanding the current framework of clinical trial regulations in India
  • Brief information for preparing for regulatory inspection
  • Be part of a major networking opportunity

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