Drug Safety and Pharmacovigilance

Drug Safety and Pharmacovigilance
Product Description

Lambda Therapeutic Research delivers comprehensive Clinical Safety and Pharmacovigilance (PV) services, seamlessly supporting clinical trials and post-marketing programs. Our well-established PV framework ensures meticulous safety monitoring and regulatory compliance for both clinical and commercial products. From early development to post-marketing surveillance, we provide end-to-end support across the entire lifecycle of medicinal products, prioritizing patient safety and global regulatory standards.
Core Services

  • Case Processing
  • Medical Information
  • Drug Safety Reporting
  • Risk Management Plans
  • QPPV Services (UK & EU)
  • Clinical Safety Management Plan
  • ASIME
  • PSURs, PADERs, ASRs, DSURs, PBRER & ACOS
  • Literature Services
  • xEVMPD Compliance
  • EudraVigilance Services
  • PV Consulting & Training
  • Medical Writing & Publishing
  • SUSAR processing & Submission
  • Signal detection, evaluation & Management
  • Global Compliance & Support for Regulatory Affairs

Lambda Therapeutic Research Ltd

  • Country/Region:
    India
  • On CPHI since:
    2015
  • Certificates:
    2
  • Employees:
    1000 - 4999
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Primary activities
Analytical Services
Clinical Research
Contract Research Organisation
Laboratory Services
Nutraceuticals
Regulatory Affairs
Specifications
  • Selling Points
    Quality Service
  • Supplied from
    Belgium; India; United Kingdom

Lambda Therapeutic Research Ltd

  • Country/Region:
    India
  • On CPHI since:
    2015
  • Certificates:
    2
  • Employees:
    1000 - 4999
Company types
CMO/CDMO
Contract Research Organisation (CRO)
Primary activities
Analytical Services
Clinical Research
Contract Research Organisation
Laboratory Services
Nutraceuticals
Regulatory Affairs

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