Whether you are seeking Regulatory Approval in a rapidly expanding European Market or require expert Regulatory Affairs / Pharmacovigilance advice and support, Unicus are the Regulatory Affairs Specialists you need.

Viewed by many of it's Pharmaceutical clients as the first port of call for all their European Regulatory Affairs and Pharmacovigilance requirements.

Founded in 1996 Unicus has developed a range of services to meet the rapidly changing demands of Regulatory Affairs, Pharmacovigilance and the demand for timely project completion, from strategic planning and expert Pharmacovigilance advice to hands-on regulatory submissions or specialist Regulatory Affairs consultants on client premises.Unicus provide the following services:

Regulatory affairs, regulatory affairs specialist, regulatory affairs consultants, regulatory affairs consultancy, reg affairs,
Pharmacovigilance, Pharmacovigilance specialists, Pharmacovigilance consultants, PV, pv, Pharmacovigilance inspections
ctd,
Readability testing, user testing, pil testing, pil user testing, patient information leaflets,
coaching and development,
report writing, medical report writing,
safety reporting, adverse drug reaction, electronic reporting, ectd, electronic publishing, toxicology.

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