Our aim is to provide assistance in:
Qualifications within the team include:
Clinical Drug Trials Reporting (UK) - Clinical event reports for clinical drug trials (UK) spontaneous reports (UK clinical trials for Europe, England, Scotland, Wales and Irland). Europe, EU Clinical Drug Trials - Processing adverse event reports from clinical trials. Our aim is to provide assistance in:
Clinical Drug Trials Reporting (UK) - Clinical event reports for clinical trials (UK) spontaneous reports (UK clinical trials for Europe, England, Scotland, Wales and Irland). Europe, EU Clinical Drug Trials - Processing adverse event reports from clinical trials. Our aim is to provide assistance in:
Processing adverse event reports, both spontaneous and from clinical trials. Processing of Product Technical Complaints on Medical Devices. Preparation of Periodic Safety Update Reports. Writing standard operating procedures and working practices. Management of the pharmacovigilance process. Continuous improvement and business process re-engineering to reduce costs and insure compliance. Processing adverse event reports, both spontaneous and from clinical trials. Processing of Product Technical Complaints on Medical Devices. Preparation of Periodic Safety Update Reports. Writing standard operating procedures and working practices. Management of the pharmacovigilance process. Continuous improvement and business process re-engineering to reduce costs and insure compliance.
Clinical Trials Reporting (UK) - Clinical event reports for clinical trials (UK) spontaneous reports (UK clinical trials for Europe, England, Scotland, Wales and Irland). Europe, EU Clinical Trials - Processing adverse event reports from clinical trials.
Processing adverse event reports, both spontaneous and from clinical trials. Processing of Product Technical Complaints on Medical Devices. Preparation of Periodic Safety Update Reports. Writing standard operating procedures and working practices. Management of the pharmacovigilance process. Continuous improvement and business process re-engineering to reduce costs and insure compliance. Processing adverse event reports, both spontaneous and from clinical trials. Processing of Product Technical Complaints on Medical Devices. Preparation of Periodic Safety Update Reports. Writing standard operating procedures and working practices. Management of the pharmacovigilance process. Continuous improvement and business process re-engineering to reduce costs and insure compliance. UK Clinical Trials (British Clinical Trials, UK) - Clinical event reports for clinical trials (British, UK) spontaneous reports (British, UK clinical trials London, Bristal, Birmingham, Manchester, Canterbury, Glasgow, Sandwich and Other British Places). British Europe, EU Clinical Trials - Processing adverse event reports from clinical trials
Processing adverse event reports, both spontaneous and from clinical trials. Processing of Product Technical Complaints on Medical Devices. Preparation of Periodic Safety Update Reports. Writing standard operating procedures and working practices. Management of the pharmacovigilance process. Continuous improvement and business process re-engineering to reduce costs and insure compliance. Processing adverse event reports, both spontaneous and from clinical trials. Processing of Product Technical Complaints on Medical Devices. Preparation of Periodic Safety Update Reports. Writing standard operating procedures and working practices. Management of the pharmacovigilance process. Continuous improvement and business process re-engineering to reduce costs and insure compliance. Clinical Trials and Clinical Trials Europe EU.
