A registry to collect information on pregnancies that occur after the use of ellaOne® (ulipristal acetate).

Participation in the registry is voluntary

All personal data is handled in accordance with applicable data protection laws. The information you provide will be kept strictly confidential, stored securely, and used solely for safety evaluation and regulatory reporting.

You may participate if:

You are pregnant after using ellaOne®, or

You are a health care provider treating a pregnant patient who has used ellaOne®.

Please select the option that applies to you:

I am a Patient
I am a Health Care Provider