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PRODUCTION- Maintain Compliance
through the Product Lifecycle

Easily Find Ingredients

Identify and track the location of all your ingredients, ingredient attributes, substances and documents for each product using the IIN’s ‘Where Used’ feature.

IIN R&D

Eliminate Manual Processes

Save time and money by integrating regulatory content and import tracking directly with your Product Life-cycle Management (PLM) system.

View the Whitpaper

Receive Regulatory Updates

Stay up-to-date with regulatory changes and get notified immediately if any of your products are impacted by changing regulations.

Take Control of Compliance

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.

Quickly share documentation

When it comes to keeping track of product documentation, it’s no longer a matter of who, what, where and when. The IIN includes custom confidentiality settings, so only relevant parties have access to your intellectual property. Document status history is automatically captured and made available to you in real time. See when document requests were made, when they were received, who made modifications and when they were made.

Document Management Video Download Fact Sheet

Stay on top of compliance after product launch

With the IIN’s regulatory surveillance function, you know up front if any of your products are impacted by changing regulations. In addition to quarterly updated reports, you’ll be able to monitor your products’ compliance history, manage documents and track product information and changes through all stages of the product life cycle. 

View Jurisdictions

Quickly find where ingredients are used across entire product portfolio

It’s tough to know where an ingredient, ingredient attribute or substance is located in your product portfolio, especially if you have a large number of products. The IIN’s Where Used search feature allows you to run your own search filters with criteria such as ingredient name, Raw Material, substance or raw material supplier. Search to view which formulas contain certain substances or raw materials or where a substance appears in a formula or raw material. All search results can be categorized and exported into a spreadsheet for easy visibility.

Document Management Video

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!

NPD Wheel
Ideation Development Evaluation Execution Production Development Evaluation Execution Production

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?

Learn More

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?

Learn More

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?

Learn More

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?

Learn More

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?

Learn More

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?

Learn More

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?

Learn More

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?

Learn More

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?

Learn More

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Blog

New Opinions on Chemical Safety in Consumer Products Released by UK Scientific Advisory Group

March 30, 2023 by Ithos Global Regulatory Team

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

March 30, 2023 by Ithos Global Regulatory Team

Last Updated on March 30, 2023 by Ithos Global Regulatory Team The FDA has released two major updates in response…

Webinars

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…

44 minutes Sign Up

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…

60 Minutes Sign Up
Glossary

PIF

“Product Information Form” industry or jurisdiction-agreed standard format for capturing key product details (e.g. PIFs per EU regulation 1223/2009)

RIPT

“Repeated Insult Patch Test” – irritation testing required of products coming in contact with skin.

CLP

“Classification Labeling and Packaging” In the EU, CLP allows for the identification of hazardous chemicals and the communication of these…

Education

Webinar: MoCRA Explained

Submit the form below to access the webinar. Need the password? Click here.

Watch Video

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…

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Troy, NY, 12180

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