NeoCubes has a global presence through which we are capable of providing comprehensive clinical and post marketed safety services that include complete pharmacovigilance services, which includes aggregate report writing, signal detection and management, global literature surveillance, risk management, case processing and reporting.

We can support you for below markets:

  • Europe/UK Market

  • US Market

  • RoW Market

NeoCubes offers global Drug Safety/Pharmacovigilance service combined with specific consultancy and assistance throughout product development and marketing life cycle to meet Pharmacovigilance needs of generic pharmaceutical industries.We have extensive knowledge in below activities specifically;

  • Complete PV setup according to country specific requirement

  • Case search and sourcing

  • Case processing and Case/Safety Reporting

  • Services of EU QPPV, country specific local QPPV

  • PSMF preparation and it’s Maintenance

  • Signal Detection

  • Drafting and submission management of aggregate safety reports like PSUR, PBRER, PADER, Clinical Overview and DSURs

  • Comprehensive Pharmacovigilance Service Packages for the RoW Region

  • Medical information Call Centre (Require to collect Adverse events, Product complaints, Medical information and this is for 24 X 7 Support)