As Pharmacovigilance Auditing and Regulatory Affairs experts, we're here to act as your partner for all drug development issues, offering comprehensive advice and support based on numerous years of experience.

VigiReg provides EU Regulatory Affairs support.
VigiReg's Director of Regulatory Affairs is Rita Anna Kużel. Rita is a Polish and UK national and has a PhD in drug metabolism. She has over 25 years of Regulatory Affairs experience both in small and large pharmaceutical companies.

In her role at VigiReg, Rita is involved in assisting drug developers to seek European Scientific Advice, attend Health Authority meetings and compile EU Marketing Authorisation Applications for a variety of medicinal products.

For any questions, please contact us at:

Address:

VigiReg Consulting Sp. z o.o

Slawoszyno, POLAND

Tel: +48 600 131 484

or

VigiReg Consulting Ltd.,

Amersham, United Kingdom

Tel: +44 7973 770 712

or E-mail:

keith.wibley@vigireg.com

You can also use our contact form.