Summary
Overview
Work History
Education
Skills
Certification
References
References
Personal Information
Affiliations
Systems & Tools
Timeline

Ravikumar Tailor

Summary

Accomplished professional with extensive expertise in pharmacovigilance and regulatory compliance, specialising in QPPV oversight management and PV system management. Demonstrates proficiency in regulatory submissions, audit readiness, and SDEA compliance, ensuring alignment with MHRA and EMA frameworks. Adept at safety database oversight, inspection readiness, and internal audits, with a proven track record in CAPA development and tracking. Skilled in PSMF maintenance and stakeholder liaison, contributing to SOP development and process improvement initiatives. Committed to advancing career goals through continuous enhancement of industry knowledge and operational excellence.

Overview

16
16
years of professional experience
1
1
Certification

Work History

Deputy UK QPPV & Senior Manager

Lambda Therapeutic Ltd
London
10.2021 - Current
  • Supported UK QPPV with day-to-day PV responsibilities and acted as backup during unavailability for more than 15 Clients.
  • Maintained oversight of the safety profile for multiple MAH portfolios, including review of PSURs, RMPs, signal reports, and risk minimization activities.
  • Coordinated timely regulatory submissions and safety updates in line with MHRA and EU GVP requirements.
  • Monitored PV system performance through compliance metrics and initiated quality improvement strategies.
  • Led MHRA inspection preparation, served as inspection lead, and managed post-inspection CAPAs.
  • Delivered regulatory intelligence updates on monthly basis.
  • Acted as inspection lead for MHRA Inspection and client audits; coordinated CAPA planning and implementation.

Key Achievements

  • Built strong partnerships with stakeholders for mutual benefit.
  • Successfully deputized UK QPPV during MHRA interactions and regulatory inspections.
  • Implemented a risk-based compliance framework that enhanced QPPV oversight and inspection readiness.
  • Played a key role in adapting the PV system to meet Windsor Framework and Brexit-related regulatory changes.

National PV Contact Person- UK & Senior RA Officer

Torrent Pharma (UK) Ltd
Crawley
04.2020 - 10.2021
  • Acted as primary liaison between UK affiliate, global PV team, and MHRA.
  • Managed PSUR/RMP submissions and supported signal and variation tracking.
  • Led RA and PV support for generics regulatory lifecycle activities, while mentoring and managing key projects independently. Maintained accurate regulatory databases and ensured XEVMPD compliance.
  • Ensured compliance post-Brexit through risk assessment and Planning.

Key Achievements

  • Successfully led PV inspection activities and enhanced RA/PV documentation standards.
  • Promoted ahead of cycle due to leadership in regulatory submissions and compliance support.

Deputy PV Responsible Person & RA Officer

Torrent Pharma (UK) Ltd
Crawley
09.2018 - 03.2020
  • Managed regulatory lifecycle activities (renewals, variations) and PV obligations for more than 100 MAs.

Regulatory Affairs Associate

P.I.E Pharma Ltd/DrugRus Ltd/ Dawa Ltd
London
02.2010 - 08.2018
  • Supported end-to-end PV compliance and RA lifecycle management for generics more than 30 MAs.
  • Acted as PV contact for outsourced QPPV and coordinated safety submissions and PSMF maintenance.
  • Served as person responsible for all in-house PV activities.

Key Achievements

  • Played a central role in MAH (GxP) inspections and RA-PV system updates.

Education

MSc - Pharmacology (2:1)

Nottingham Trent University
01.2008

Bachelor of Pharmacy - 2:1

Pune University
01.2007

Diploma - Clinical Research

Catalyst Clinical Services
01.2007

Postgraduate Diploma - Pharmacovigilance

University of Hertfordshire
01.2017

Skills

  • QPPV oversight management
  • PV system management
  • Regulatory submissions
  • Audit readiness
  • SDEA compliance
  • Safety database oversight
  • Inspection readiness
  • Internal audits
  • CAPA development and tracking
  • MHRA alignment
  • EMA framework compliance
  • PSMF maintenance
  • Stakeholder liaison
  • SOP development
  • Process improvement knowledge

Certification

  • European Pharmacovigilance Congress (2025)
  • EMA/HMA Multi-Stakeholder Forum on EudraVigilance and Signal Detection (2025)
  • DIA: From Intelligence to Innovation - The QPPV’s Role in AI and Regulatory Vigilance Confirmation (2025)
  • ABPI Code of Practice – Wilmington Healthcare (2019)
  • MHRA GVP Symposia, Windsor Framework Webinars (2020–2024)
  • EMA Webinars: Signal Management, IRIS, XEVMPD
  • US-FDA | MHRA | Health Canada Joint PV Symposium (2024)
  • Organisational Leadership in the ERA of AI (2025)
  • The Data Science of Healthcare, Medicine, and Public Health (2025)

References

Available upon request

References

References available upon request.

Personal Information

Affiliations

Member, Royal Society of Biology (MRSB)

Systems & Tools

MHRA RAMA XL, CESP, EudraVigilance, XEVMPD, Extedo eCTD, IRIS, Safety Database Platforms

Timeline

Deputy UK QPPV & Senior Manager - Lambda Therapeutic Ltd
10.2021 - Current
National PV Contact Person- UK & Senior RA Officer - Torrent Pharma (UK) Ltd
04.2020 - 10.2021
Deputy PV Responsible Person & RA Officer - Torrent Pharma (UK) Ltd
09.2018 - 03.2020
Regulatory Affairs Associate - P.I.E Pharma Ltd/DrugRus Ltd/ Dawa Ltd
02.2010 - 08.2018
Nottingham Trent University - MSc, Pharmacology (2:1)
Pune University - Bachelor of Pharmacy, 2:1
Catalyst Clinical Services - Diploma, Clinical Research
University of Hertfordshire - Postgraduate Diploma, Pharmacovigilance
Ravikumar Tailor