EXECUTION- A Single Source of Truth
Effortlessly Manage Docs
Eliminate time spent gathering, managing, and updating information with a single, centralized platform.
Quickly Author Reports
Don’t waste time organizing and uploading Safety Data Sheets into your PLM or ERP systems.
Search & Find Missing Docs
Quickly find gaps in documentation so you can collect, manage and share product information with suppliers and vendors. Easily generate full PIFs for registrations.
Find Ingredients, Build Compliant Products, Access Documents Easily
The IIN is the only ingredient, regulatory, and document management software, which enables you to create compliant products from the start.
Accelerate product registration
The IIN PIF module automates the search and retrieval process of documents, making it much easier to compile dossiers for submission to global regulatory authorities. From retrieval of documents to filing and submission, the IIN helps you manage the entire process of creating your dossier.
Take control of SDS authoring
Our self-authoring tool, IngredientSAFE, is a fast and cost-effective way for your team to author SDSs on their own time, whenever they need them. Using Ithos’ global, standardized template, you can author SDSs for both the US and EU in 7 languages – without the need to outsource regulatory consultants.
Don’t let missing documents hinder your product registrations
The IIN’s Document Manager module is designed to quickly find what you’re looking for. Ithos’ supplier outreach function collects all requested documents and stores them in a centralized location for quick retrieval at any time throughout the product life cycle. Reduce your team’s time spent searching and eliminate manual processes that often result in incomplete or inaccurate documents.
What Stage are you at in New Product Development?
NPD Wheel
Click around the spokes of the Ithos NPD Wheel to learn more about each stage!
Ideation
Is it difficult to get everyone on the same page for new product development?
Do you receive incomplete marketing briefs? Or miss changes made to it after the fact?
Development
Do you have trouble tracking the various tests for formulas or knowing what testing is needed?
How do you track the reasons for reformulation?
Need to find alternative ingredients?
Evaluation
Do you have trouble gathering missing documents for your RMs?
Does it take you too long to review formulas for global compliance?
Is it hard for you to stay on top of the changing ingredient laws?
Execution
Are you missing documents needed for product registrations?
Does it take a lot of time for you to gather missing documents?
Do you need SDSs quickly, last minute?
Production
Do you find yourself facing the costs associated with noncompliance due to an ingredient ban or usage restriction?
Have you experienced difficulty maintaining compliance with changing regulations that require additional reporting?
Is it hard to find where an ingredient is used across your product portfolio?
Do you often miss expired docs until you need them?
Is it difficult to track finished good imports and the required data points?
Development
Do you have trouble tracking the various tests for formulas or knowing what testing is needed?
How do you track the reasons for reformulation?
Need to find alternative ingredients?
Evaluation
Do you have trouble gathering missing documents for your RMs?
Does it take you too long to review formulas for global compliance?
Is it hard for you to stay on top of the changing ingredient laws?
Execution
Are you missing documents needed for product registrations?
Does it take a lot of time for you to gather missing documents?
Do you need SDSs quickly, last minute?
Production
Do you find yourself facing the costs associated with noncompliance due to an ingredient ban or usage restriction?
Have you experienced difficulty maintaining compliance with changing regulations that require additional reporting?
Is it hard to find where an ingredient is used across your product portfolio?
Do you often miss expired docs until you need them?
Is it difficult to track finished good imports and the required data points?
Trusted by Leading Cosmetics Organizations
Subscribe to Our Newsletter
Sign up to receive updates from Ithos Global, including information about upcoming events, regulatory news, and more.
New Opinions on Chemical Safety in Consumer Products Released by UK Scientific Advisory Group
Last Updated on March 30, 2023 by Ithos Global Regulatory Team The Scientific Advisory Group on Chemical Safety (SAG-CS) in…
MoCRA Updates: FDA to ‘Sunset’ VCRP and New ORA Restructuring
Last Updated on March 30, 2023 by Ithos Global Regulatory Team The FDA has released two major updates in response…
IT Security Considerations For Your Cosmetic information Management Systems
In this fast-paced world of technology and software development, it is more important than ever for companies to have the…
Using Data and Screening Tools to Commercialize your Products
In recent years, more cosmetic companies are realizing the greater need to organize products, formulas, and raw material documentation and…
CARB
“California Air Resource Board” CARB requires registration of consumer and commercial products.
SCPN
“Submit Cosmetic Products Notification” (UK portal for cosmetic notification)
EC#
EU-specific, seven digit substance registration number with pattern xxx-xxx-x, either Einecs, Elinecs, No-Longer Polymers databases.
Webinar: MoCRA Explained
Submit the form below to access the webinar. Need the password? Click here.
Guide: How to Prepare for MoCRA
Ready to tackle MoCRA and get ahead of the game? View our guide to learn how you can start preparing…
