Product Stewardship

Global companies manufacturing and selling across multiple jurisdictions must develop detailed regulatory strategies to avoid unnecessary testing while aligning regulators' review and marketing timelines. Marketing professionals work hand-in-hand with both Research & Development and Product Stewardship experts to secure successful new product launches.

Regrettable substitutions of Substances of Very High Concern, undesired classifications of substances in a late development stage, or delayed regulatory submissions due to wrong substance identities are just a few of the pitfalls. The substitution of BPA with BPS in specific applications and the launch of GenX as a more acceptable alternative to PFOA are only a few examples of costly mistakes based on wrong judgments of regulatory developments.

Our experts anticipate regulatory trends and provide in-depth insight into many global jurisdictions' regulatory requirements, helping clients make the right decisions and supporting every step in obtaining the necessary regulatory approvals.

We deliver services in:

Regulatory compliance auditing and Due Diligence to Private Equity Firms.
Global registration and notification of substances (EU-REACH, TSCA, "REACH-like" Regulations).
Authoring of white papers supporting communication to regulators, policymakers, or the general public.
Advocacy and representation services with industry associations or regulators.
Regulatory Trend Reports.
Substance Identity, fingerprinting, and contamination profiles.
GHS classification & labeling.
Creating chemical regulatory overviews and interpretations.
Export and import advice on chemicals.
Hazard, Exposure, and Risk Assessment.
Safety Datasheet review and authoring.

We network with experts offering integrated software architectures enabling SDS and Label authoring in 50+ languages for all major jurisdictions using for example, LISAM's ExESS software integrated into SAP EH&S or any other solution.

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