Our services
Regulatory support with precision and confidence
MAx RegConsult offers qualified services for pharmaceutical companies in Regulatory Affairs, Pharmacovigilance and Quality & Processes - from development to life cycle management.
Our strength lies in long experience, accuracy and the ability to quickly understand each customer's unique needs.
Regulatory Affairs (RA)
We handle applications, labelling and artwork for the Nordics/EU - with a focus on speed, quality and compliance.
Pharmacovigilance (PV)
Full service in PSUR, RMP, ICSR and literature monitoring, both globally and locally.
Quality & Processes (QA)
QMS, SOPs, CAPA, supplier controls and audit - all under full confidentiality.
Regulatory support from development to life cycle management
MAx RegConsult offers flexible arrangements for insourcing, outsourcing and interim management -
with a focus on high quality, fast delivery and full compliance.
