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