With a commitment to delivering tailored solutions and actionable insights, I support Pharmaceutical, Biotech, Med-tech Companies and their CRO’s to unlock their full potential and achieve reliable outcomes in clinical trials.

Services range from design and implementation of

• Innovative compliance framework (QMS),

• Risk and Quality Based Design of studies

• Leadership and transformation of departments

• Project Management

• Protocol and essential documents, Informed Consent, CRFs

• Site start up

• Clinical trials conduct, monitoring, central data surveillance

• Data Management, eCOA set-up

• CMC and other study supply alignment

• Quality Control

• Digital solution design & implementation

• Change management

• Financial control

• Individual and Team performance management

• Risk Management

• Global, international

• Innovative, fit-for-purpose solutions