An efficient and intuitive platform to facilitate hazard identification and chemical approval, stay in compliance with EPA and OSHA regulations, and promote safe workplace conditions on site.
Substitute long email chains and undocumented phone calls for configurable approval forms and straightforward review workflows
Track a product's change history for chemical managers, EHS managers, regulatory review officers, and vendors to see in one place
Assign approvers, notify involved parties and supervisors, track approval status, and record approved products... all automatically
ERA's Product Approval management software is the best way to expedite your chemical and material approval processes, ensure effective tracking, and avoid setbacks in product development across facilities.
Standard form templates show all the fields required for effective data entry, but they can also be modified to suit the type of data you want to gather and restrict progress if certain questions aren't answered.
Chemical and EHS Managers receive automated alerts every time a step is completed, a request is denied, a roadblock is flagged, information is requested from the manufacturer, and the product or chemical gets approved.
View linked chemical regulations—TSCA, SARA 313, Homeland Security Chemicals of Interest, etc.—in one query.
Automated data collection and management lets you eliminate spreadsheets and manual data tasks.
Your product approval data integrates with other key management tools from ERA's software offer
***Other modules must be purchased separately***
Transfer your products' chemical formulation to your inventory reports, like Tier II, and avoid entering the same data twice
The system pulls the information stored in your products' SDS from ERA's SDS Management and SDS Authoring modules
Our MCL tracks over 200,000 chemicals and toxic categories to determine the exact composition of your products
Chemical Managers no longer have to go through redundant re-approvals for products used consistently, no matter which facility they end up in or whether they are delivered in different containers or across multiple storage and inventory locations..
Suppliers across any industry can skip the data entry process for already-approved products.
Vendors can add their product's information, including physical and chemical properties, directly into the software, seamlessly initiating a material approval request that is easy for reviewers to approve and easily scales for their entire chemical inventory.
EHS Managers have access to the same database (if allowed by access rights reflecting corporate hierarchy) where on-site products are assessed and accounted for, thus expediting approval and reducing compliance risks.
Yes, ERA provides users with optimized templates and tracking tips in their comprehensive training courses. You will undergo these trainings in your requested onboarding process with dedicated experts.
Find out how ERA satisfies most of your EHS needs.
Any other questions?
Contact us
Centralize approvals with ERA-EHS to implement a risk-based review path, link regulations, and document sign-offs to support regulatory compliance. Doing so helps reduce unmanaged risk, strengthen chemical safety decisions, and create an auditable record for OSHA and EPA programs.
You’ll need to submit the product’s safety data sheets (SDSs), any supporting safety data, and other available data sheets. From there, information such as intended use, storage location, and quantities is also vital to track. ERA-EHS provides a platform that captures structured data, identifies applicable chemicals, and ties data into your chemical inventory for downstream inventory and reporting needs.
With ERA-EHS, easily grant role-based access for suppliers, manufacturing teams, and reviewers so that each party can contribute while being restricted to what they own. Status tracking, automated alerts, and real-time visibility help manage approvals across sites without losing content, no matter how complex the industry workflows are.
ERA-EHS chemical management software ensures that approved products are properly managed to support reporting, chemical inventory management, and other tasks without re-entering the same information. Maintaining data continuity across your organization helps achieve efficient and accurate regulatory reporting, risk management reviews, and waste management tracking, all while keeping approvals aligned with the current product formulation.