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Mammalian Toxicology
Our Toxicology service provides end-to-end toxicological expertise to help companies meet regulatory requirements and assess the human and environmental safety of chemicals, including complex and challenging substances.
Combining scientific rigour with regulatory insight, we offer tailored testing strategies, study design and monitoring, dossier assembly, NAMs, and regulatory support to deliver robust, defensible data, reduce risk, and secure compliant market access.
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At Penman Consulting, we combine scientific expertise with practical insight to help our clients navigate complex challenges with confidence. Our approach is built on six pillars.
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Ensure full REACH compliance with our end-to-end services, from substance identification to authorisation support. Partner with our expert team to navigate global regulations and bring your products to market with confidence.
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Digital Product Passports in 3 Minutes
What the EU Ecodesign Regulation really means for manufacturers
Within the next few years, selling certain products in the EU will depend on your ability to produce a Digital Product Passport.
Digital Product Passports (DPPs) are a core part of the EU’s Ecodesign for Sustainable Products Regulation (ESPR) and other product-specific regulations (e.g. the Detergents and Surfactants Regulation). With the objective of increasing product data transparency and enabling circularity, there will be direct implications for companies marketing products. Indirectly, these will extend upstream to manufacturers and importers.
What will be required?
While the detail will vary by product category, the direction is clear.
Manufacturers will need to provide reliable, structured information on:
- Materials and substances within products
- Environmental impact, such as carbon footprint
- Durability and repairability
- Compliance with regulatory restrictions
- End-of-life handling, including reuse, recycling and disposal
This information must be:
- Digitally accessible
- Consistent across markets
- Available to multiple stakeholders
And importantly, it must be kept up to date. This is not a one-off declaration; it is an ongoing obligation.
The shift this creates
Historically, product information has been fragmented across teams and systems, stored in documents and spreadsheets, and updated only when needed. DPPs change that dynamic.
Product data becomes visible beyond your organisation, subject to scrutiny, and expected to be consistent and current. In effect, it moves from internal reference material to externally relied-upon evidence.
Moving DPPs from theory to reality
The supply chain is expected to apply pressure first. Before regulators act, your customers will. Larger manufacturers and retailers will increasingly require DPP-compatible data from suppliers, along with confidence that products are compliant and defensible.
The practical question to ask
For most organisations, this comes down to a simple test: can we confidently explain what is in our product, and keep that answer up to date? If the answer depends on chasing multiple teams, interpreting documents or rebuilding information each time, then DPPs will be difficult to sustain.
A pragmatic way to respond
Waiting for complete regulatory clarity is understandable, but risky. An alternative is to start building capability now. Understand what product data you already have. Identify gaps and inconsistencies. Improve how that information is maintained. Engage suppliers earlier.
The goal is not perfection. It is to move from reactive, manual processes to reliable, maintainable product information.
AI in Chemical Compliance: A Case for Caution
As Chief Technology and Product Officer, I spend a lot of time thinking about where technology can create real value for our clients, and where it risks creating more noise than progress. AI is one of those areas where both are true.
ECHA's Latest Update: New Proposals to Identify Substances of Very High Concern
The European Chemicals Agency (ECHA) has initiated 14 new public consultations on testing proposals, with a submission deadline of 16 October 2025. These consultations are part of ECHA's ongoing efforts to identify Substances of Very High Concern (SVHCs) under the REACH Regulation. The inclusion of a substance in the SVHC Candidate List can trigger regulatory obligations, including authorisation requirements and communication in the supply chain.
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