Conference Details

13th Global Pharmacovigilance And Clinical Trials Summit

  • Health and Medicine
  • Conference
  • Mar 29, 2019 - Mar 29, 2019
  • Hyatt Regency Osaka Nankokita, 1-13-11, 〒559-0034 Osaka Prefecture, Japan
  • Osaka, Japan
  • Rating:
Paper Submission Date
Registration Date
Acceptance Notification Date


With the excellent accomplishment of Pharmacovigilance Series of Conferences in the UK, the USA in back to back a long time in the course of the most recent quite a while which met with extraordinary accomplishment in Business Conferencing. It's happy to report thirteenth Global Pharmacovigilance and Drug Safety Summit amid March 28-29, 2019 Osaka, Japan with the topic ‘’Promulgating the prevention of adverse drug reaction". This is a 2-day Mega Event offering Exhibition, at the scene to grandstand the new and rising advancements with Keynote introduction, Oral, YRF (Student Presentation), blurb, e-publication Presentations.


We are happy to educate you that the Speaker/Delegate/Exhibitor openings are accessible at the meeting. kindly visit the website of the conference to find out about the scientific sessions and abstract submission, If needs to go to as Delegate, sympathetically enroll to the gathering. For any questions, mail us.

Keynote:(Day 1)


Dr.Jacob Joseph, Harward Medical School, USA

Dr.Ujwala Salvi, Nucleon Therapeutics, India

Dr.Omer, Sanofi, Canada

Dr.Ashok, Clinfomatrix, USA


Other Speakers

Mr.Chi Chen, E&Y, China

Dr.Meenal Patwardhan, Abbvie, USA

Mr.Rajiv Joshi, E&Y, India



Keynote (Day 2)

Dr.Essam, Celyad, Belgium

Dr.Carole, Sun Pharma, Japan

Mr.Robert, Accenture, Spain

Session Speakers:


Mr.Ravish Kumar, Salzman Group, Australia

Dr.Abdeen, Ministry of health, UK.

Dr.Ripal Gharia, Cliantha research, India

Mr.Mohammed Gayoor khan,NFPS,Malaysia



List of Main Topics

  • Pre-Clinical and Clinical Trials
  • Adverse Drug Reactions
  • Good Pharmacovigilance Practice
  • Drug Safety
  • Clinical Trial Protocols
  • Diversity in Industrial Clinical Trials
  • Clinical Research and Statistics
  • Clinical Database Management
  • Medical and Clinical Case Reports
  • Hospital and Industrial Pharmacy
  • Clinical Data Management and Analytics
  • Clinical Trial Site Selection and Management Medical and Clinical Case Reports
  • Biopharmaceutical Sciences
  • Drugs Regulations.


Dr.Jacob Joseph

Dr.Meenal Patwardhan



Submission Instructions

Abstract Submission portals are open now

Submit your abstract at

Submission Dates

Abstract Date

Registration Fee and Instructions

Registration ; $799 

Package A : $1099(includes 2 nights accomodation)

Package B : $1249(includes 3 nights accomodation)

Follow the link :


Accommodation will be in the venue of the conference.

For queries contact at Zoey Williams -globalpharmocovigilance2019@gmail,com

Exhibit Information

The 13th Global Pharmacovigilance & Clinical Trials Summit will exhibit the products and services from commercial and non-commercial organizations like Drug manufacturers, Clinical Trial Sites, Management Consultants, Chemists, Pharmacists, Business delegates and Equipment Manufacturers.

More details :