Experienced Pharmacovigilance physicians with expertise in medical review, assessment of safety data (from post marketing signal evaluations to clinical trial data sets), MedDRA coding, risk assessment and benefit risk evaluation. Our medics are happy working as part of a vibrant Pharmora team to deliver your services or they would be equally happy working within your teams to support your deliverables.
Scientists with Pharmacovigilance expertise who can support your business at the level your require. They are happy working within a vibrant team supporting Pharmora medics, drafting regulatory standard documents such as DSUR, PBRER (PSUR), risk management plan, submission modules and any other routine global Pharmacovigilance documentation. Pharmora scientists range from those skilled in data entry to those who can lead safety surveillance activities including safety management team leaders.