Basic info
Industry
pharmaceutical manufacturing
Sectors
Rx – to – OTC switch
Drug life cycle management
Pre-authorisation services
Human medical products
Preclinical and clinical development
ATMP
GLP
Drug development
Pharmacovigilance system
Audits (GMP
Audits of API manufacturers
organization and monitoring of trials
In-/out-licensing support/broker
Leaflets readability tests
Medical devices and biocides
Post-Brexit support
Registration process management
Pharmaceutical consulting services
PHV)
GCP
Post-authorisation
Planning
Regulatory affairs
Regulatory and medical writing
Date founded
2004