International Conference on
Pharmacovigilance and Regulatory Affairs
March 24-26, 2025 | Rome, Italy
- Authors are invited to submit abstracts through the Conference Submission Systems, Click the Submit Abstract Button Below.
Scientific Board
Aim
Our aim to bring together leading academic scientists, researchers and research scholars to exchange and share their experiences and research results on all aspects of Pharmacovigilance and Regulatory Affairs.
Objective
To provide a premier interdisciplinary platform for researchers, practitioners and educators to present and discuss the most recent solutions adopted in the fields of Pharmacovigilance and Regulatory Affairs.
Dates to remember
Abstract Submission Deadline
October 15, 2024
Early Bird Registration
September 28, 2024
Conference Dates
March 24-26, 2025
About Conference
We are pleased to announce that the International Conference on Pharmacovigilance and Regulatory Affairs will be held on March 24-26, 2025 at Rome, Italy.
On behalf of
the Organizing Committee we take great pleasure to cordially welcoming you all
academic scientists, researchers, research scholars, students and experts of
application fields to Rome, Italy for the International Conference on
Pharmacovigilance and Regulatory Affairs conference to foster the progress in
the pharmacy by contributing with your expertise to what promises to be a very
comprehensive and exciting meeting, and to enjoy the immense unique artistic
heritage and wonderful landscape of Rome.
The aim of
the ICPRA-2025 is to promote quality
research and real-world impact in an atmosphere of true international
cooperation between scientists and pharmacist by bringing together again the
world class researchers, International Communities and Pharma heads to discuss
the latest developments and innovations in the fields of Pharmacovigilance and
Regulatory Affairs.
We sincerely
hope that ICPRA-2025 serves as an
international platform for meeting researchers from around the world, widen
professional contact and create new opportunities, including establishing new
collaborations.
We look forward to seeing you in ICPRA-2025 in Rome Italy.
Best regards,
Sai Lakshmi | Conference Secretary
ICPRA - 2025
Plenary Speakers
Invited Speakers
Scientific Sessions
- Pharmacovigilance and Eudravigilance
- Introduction to Pharmacovigilance (PV)
- Identification of Risk Factors
- Good Drug Development Practices
- Post-marketing surveillance
- Big data and AI in pharmacovigilance
- Drug legislation and regulations
- Benefit-risk management strategies
- Concept of drug safety
- Importance of HIV testing for early detection
Scientific Sessions
- Adverse drug Reactions Reporting
- Harmonization and pharmaceutics
- Innovative approaches to drug safety
- PV Regulations and Challenges
- Medical Devices Safety
- Adverse Drug Reactions
- Big data and AI in Drug Surveillance
- Patient Centric Drug Safety
- Drug Testing Workflows with AI & Automation
- Safety Signals & Management
Previous Glimpses
Need help now? Mail us now: icpra2025@pagesconferences.org
Book your Speaker or Delegate slot. Contact us regarding group registrations on special prices