EVALUATION – Involve Regulatory
Early On
Quickly Access Documents
From Ingredient Search to Document Management, we provide a one-stop solution for your Research and Development needs.
Involve Regulatory Early On
Our fully integrated solutions will help you ensure you are in full regulatory compliance before you launch a new product.
Step-by-Step Guidance
Create a new artwork and label review process that’s tailored to your business needs.
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.
Review formulas early in development to prevent regulatory compliance delays
Ithos’ industry-leading formulation PLM makes it easy to ensure each product is compliant with regulations before it goes to market – without missing product launch timelines. Achieve an additional level of product compliance by checking formulas against internal or leading retailer Clean Lists.
Avoid reformulation expenses with version control of formulation history, so your team can see past iterations, any red flags raised, and learn how compliance issues were solved.
Don’t delay printing product packaging
We understand the intricacies of label regulations and the IIN can guide you and your team through the entire label review process. Avoid relabeling costs and verify labeling claims quickly and easily without getting bogged down by bureaucratic red tape.
Plus, we have a team of Regulatory Experts on hand who can help you out even further.
Create Ingredient Listings in various formats
The IIN’s Ingredient Listing module was developed to meet the needs of both large and small cosmetic companies looking to create and manage their IL in a variety of formats. Using the IIN, you can easily create Ingredient Listings to comply with FDA regulations or share with your customers. Generate and export quantitative, qualitative or custom formatted ingredient listing for your own document management and compliance needs.
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?
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“Globally Harmonized System for Classification and Labeling of Chemicals” – 2003 UN protocol for standardization of information.
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“Chemical Abstract Service”. CAS assigns IDs to more than 142 million unique organic and inorganic compounds. Their database is updated…
Formula
Final product after different chemical substances are combined.
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