Cosmetic regulatory software solutions to grow your business.

Access to cosmetic and personal care regulatory information for all (or a subset) of the jurisdictions currently available within Ithos Global’s managed content offering. Receive customized reporting on a quarterly basis detailing what updates (if any) occurred during the past quarter. This includes the impacted ingredient name and cas number, the regulatory source that was updated, and other relevant information surrounding the update. Also receive detailed list of updates by source in every jurisdiction managed by Ithos.

Curated news of current and upcoming regulatory information.

Workflow to mark the process of a finished good New Production Introduction Process. View status of the tracker, assign users from multiple departments to specific steps, and easily link to other areas of the IIN.

Build experimental and final formulas with phases and processing instructions. Versioning keeps track of changes made and ensures a record of previous formulas.

Search the cosmetic regulatory content database to view details on cosmetic ingredient restrictions in various jurisdictions. Search the INCI content database to view additional details for over 25,000 INCI substances

Screen formula ingredients against select jurisdictions to see if ingredients are prohibited, restricted, or allowed. View the sources and rules within each jurisdictional tab in an interactive Excel report. Want to see an example of this report? Request a sample here.

Screen formula ingredients against internal Ingredient Policy Lists, or “no-no” lists / blacklists. Mange the lists that are screened against

Ithos will review a draft product label to determine needs prior to a final Finished Good Label Review

Store vendor documentation on raw materials, formulas, and products in an organized, central repository. View, download, upload, archive documents. Includes Address book to store vendor contact info

Generate a Qualitative Listing for a formula with logic for various jurisdiction labeling requirements

Review of a Cosmetic or Drug Label for US, EU, or Canada. Inquire for other countries.

Compile the documents needed for a PIF and build a PIF package that can be sent to a Responsible Person in a zip file small enough to email

Generate a 16 point Safety Data Sheet in GHS for the United States and Europe. 7 available languages: English, Spanish, Chinese, Vietnamese, Japanese, Canadian French, Brazilian Portuguesse

CARB reporting tool generates files to be submitted to the California Air Resources Board Portal