Unicus Regulatory Services - Regulatory Affairs, Pharmacovigilance, User Testing, pil testing, readability testing,

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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 its 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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	Unicus Regulatory Services Inspired solutions in a regulated world Regulatory Affairs Specialists
		Now as part of the Fulcrum Pharma group we are in a position to offer a number of additional services to our new and existing clients. You will now be redirected to the new company website where you will find our complete range of service offerings.

Unicus Regulatory Services - A division of Fulcrum Pharma (Europe) Ltd Company registration No. 3735819 VAT registration No. 727 5130 44 © 2007 Unicus Regulatory Services