Clinical Development, Medical Affairs and Healthcare Compliance

We provide a select suite of clinical development, medical affairs and healthcare compliance services to pharmaceutical and biotech companies.

Our clinical development expertise has played a key role in obtaining multiple health authority approvals of global and country-specific submission dossiers for multiple new medicines and line extensions. We work across all phases of clinical development, from first in man, through registration trials and into post-marketing, real world and outcomes research studies. We also work closely with our clients to provide country-specific, highly experienced and up-to-date guidance on compliance matters in support of biopharmaceutical products.