Vizen Life Sciences Europe :: Pharmaceutical Services :: vizen.eu

Who We Are

Are you looking for Audit, EU GMP, GDP or QPPV services? Not sure what to have in place for registration procedure or what your obligations as MAH on EU market are? Or would you simply welcome support for minor tasks in the field of Pharmacovigilance, Regulatory Affairs, Quality Assurance, Distribution or Business Development?

You are at the right place! Vizen Group is a global network who offer from A to Z tailored services in pharma – 15 years on market, creating The Centre of Excellence certified with GMP, EUGDP, GVP ISO 9001, PV inspected by leading EU Authorities, own EU approved Batch Release Site and registered distribution warehouses – all in place to be able to provide you with comprehensive yet cost-effective support.

Our Services

Regulatory Services

Regulatory ServicesTailored support in line with your company requirements, allowing us to provide that additional support where needed from eCTD to EU MAH, dossier compilation, exper reports, national& EU filings to complex EU & US RA strategy set up.

Pharmacovigilance

PharmacovigilanceOur EMA, FDA and ICH compliant pharmacovigilance (PV) solutions, which is, robust and cost-effective, from single support of QPPV to complex PV solution including validated PV database.

Quality Assurance

Quality AssuranceFull complex support within CMC & Quality Assurance Compliance from QP services, EU Batch Release to complex certification of EUGMP by leading EU Authorities

Business Development

Business DevelopmentOffering our clients both a domestic and international service of technical and commercial expertise to grow their business, utilising latest IMS data.

Strategic consulting

Strategic consultingStrategic pharmaceutical affairs consulting, interaction with Health Authorities with successful projet cases on OTC switching, tailored services of fully set up EU Marketing Authorisation Holder.