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Pharmacovigilance CRO

Veeda is a leading Pharmacovigilance service provider. It offers broad spectrum, high quality, flexible, cost effective and scalable safety monitoring services that can fit seamlessly into your process, meeting all regulatory compliance requirements.

We provide a global strategy for a cooperative partnership with our clients in drug safety management for US, EU, India and ROW countries. The team is powered by highly specialized pharmacy and medical professionals. We endeavor to constantly build on optimal processes complimenting client’s needs.

Our Pharmacovigilance Services Include

  • Drug safety database support (VINCURA)
  • Individual Case Safety Report (ICSR) management: Processing, Quality review, Medical review and Global reporting
  • Literature screening
  • Risk Management Plan (RMP) writing
  • Aggregate report writing - PSUR, PBRER, PADER and ACOs
  • Medical information management including call centre support
  • Preparation of Pharmacovigilance System Master File (PSMF/PvMF)
  • Qualified Person Responsible for Pharmacovigilance (QPPV), Pharmacovigilance Officer in Charge (PvOI) and Local Responsible Person for Pharmacovigilance (LRPV)
  • Extended Eudra, Vigilance Medicinal Product Dictionary (XEVMPD)/Identification of Medicinal Products (IDMP) entries and maintenance
  • Signal Detection and Evaluation
  • Pharmacovigilance Training and Consultancy
  • Recommendations for Pharmacovigilance department designing, development and improvement.
  • Pharmacovigilance Quality Assurance including SOP development
  • Audits and support for Inspections

Veeda's Safety Database

pharmacovigilance training
To help our client meet ever increasing regulatory pharmacovigilance obligation, Veeda has created unique comprehensive offering of high quality, regulatory compliant services and database, perform by highly trained professionals in cost effective manner. Our one stop Pharmacovigilance solutions can fit seamlessly into your process, meeting all regulatory compliance requirements along with the very best of Pharmacovigilance training & consultancy.
Vincura is an advanced software solution that fulfills all Pharmacovigilance and risk management requirements while ensuring global regulatory compliance with below specification:
  • Compliant with ICH and 21 CFR Part 11 guidelines
  • Integrates E2B (R3) requirement
  • Easy Data Migration - XML file import and export
  • GAMP 5 Validation

Key Features of

  • Inbuilt global scientific literature management module, interface with any literature database
  • Auto-narrative function limiting manual efforts
  • Auto-Scheduling of Aggregate reports
  • Global dictionary support (MedDRA, WHODD, etc)
  • User productivity report
  • Simple user friendly and cost effective

Value proposition of Veeda’s Pharmacovigilance Services.

  • A flexible range of safety monitoring services to precisely compliment client’s needs.
  • High-quality Pharmacovigilance services compliant with regulatory requirements.
  • A scalable operations achieving quality and efficiency objectives
  • A very cost effective pricing model

Our exemplary regulatory track record

33 times
7 times
5 times
3 times
1 times
South Africa - MCC
1 times
NPRA - Malaysia
4 times
13 times