# Enable PMDA: Multiple Marketing Authorization Holder Automation

With the 26R1 release, to support organizations when reporting cases for products with multiple Marketing Authorization Holders (MAHs) to the Pharmaceuticals and Medical Device Agency (PMDA), Veeva Safety automates the population of Japan _Case Product Registrations_ for each MAH based on _Registration Holder/Applicant_ values on _Product Registrations_. For each MAH, Vault maps all investigational and one postmarketing _Product Registration_ to domestic _Cases_ and _Localized Cases_ for Japan. This update supports generating distinct submissions based on the configured reporting rules for each MAH. Previously, Vault mapped _Product Registrations_ for only a single MAH.

This feature is Auto-on; however, some components require additional configuration. After you have configured this feature, see <a href="/en/gr/696910/#cpr-section">Complete Intake and Process Cases for the PMDA</a> and <a href="/en/gr/872016/#reg-holder">PMDA Case Field Reference</a> for more information.

## Update the Local Reporting Details Layout

<a href="/en/gr/26387/#how-to-add-object-fields">Add</a> the _Registration Holder/Applicant_ field to the _Details_ section of the _Local Reporting Details Detail Page Layout_ of the _Local Reporting Details_ object.