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adverse events reporting
adverse events reporting


adverse events reporting

Our aim is to support you in:

  • Implementation of the quality system for Pharmacovigilance (GVP modules I, II, and IV)
  • Audit of the Pharmacovigilance System
  • Preparation for Inspections
  • Continuous improvement and business process re-engineering to reduce costs and insure compliance
  • Writing standard operating procedures and working practices
  • Management of the pharmacovigilance system

adverse events reporting

Qualifications within the team include:

  • Postgraduate Diploma in pharmacovigilance: University of Hertfordshire, Hatfield
  • Lead Auditor training (Chartered Quality Institute)
  • Quality management and process control: Institute of Quality Assurance
  • Implementing ISO9001: (Chartered Quality Institute)
  • Data processing and database management
  • Teaching in the Life Long Learning Sector e-commerce | hot ideas | cool websites
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