Tell us what you need to submit.

Share the substance, product context, intended market and regulatory requirement. We will review the request and confirm the appropriate scope.

Start with the essentials

One email is enough to start the scope review.

For an ERA, PDE, OEL or regulatory toxicology request, include as much of the following as available:

✓Active substance / API

✓Product or dosage form

✓Intended market (EU / UK / other)

✓Submission or regulatory requirement

Existing report profiles: share the substance and intended product / market so applicability can be reviewed before delivery.