Ad Hoc Clinical's consultants can:

• Assist Sponsors/CRO/Sites with SOP writing and/or review;

• Guide you through country-specific regulatory pathways for clinical trials (drugs), clinical investigations (devices) or performance evaluations (in vitro diagnostics);

• Provide information on country-specific submission requirements;

• Assist in compiling your Medical Need Program documentation;

• Organize trainings for Sites/your staff/your management;

• Do ICH-GCP audits, quality checks, TMF review;

• etc.