CLINICAL DEVELOPMENT

Expertise in all aspects of clinical trials, including planning, organising, implementing, leading, controlling, and reporting Phase I-IV studies with innovative drugs, biologics, and devices.

• Global clinical development strategy

• Assess clinical trial programme feasibility

• Review scientific proposals

• Third party vendor selection and management

• Experience in drugs for rare diseases and biosimilars

• Post-marketing surveillance

• Registries

• Regulatory support

• Strategic Fit

• Gap Analysis