Experience Drug Safety offers freelance activities in the field of Drug Safety and PharmacoVigilance Pharmaceutical Industry and its Contract Research organisations can benefit from extensive experience in triage, data entry, data processing and QC of SAE/AE data (both from clinical trials and spontaneous reports). Assistance can be offered in case submissions (including EudraVigilance and WebTrader reporting), writing of PSURs, FDA Periodic Reports, Annual Reports and DSURs.