pharmaceutical

Engineered for the World’s most Regulated Industry

From APIs to packaging, pharmaceutical supply chains are complex. Rising disclosure norms mean buyers, regulators, and investors expect verifiable, audit-ready, batch-specific carbon data.

Book a Demo
TESTIMONIAL

Building a Low-Impact Future for Pharma

CONTEXT

Real impact starts with Batch-level Clarity

Missing Data, Incomplete Footprints

APIs, intermediates, and packaging span complex supply chains. Without supplier data, Scope 3 footprints stay incomplete and miss key hotspots.

Upstream Emissions are the biggest Blind Spot

Tap
Manual Updates mean Slower Reporting

Ingredient and process changes need manual recalculation. This slows sustainability teams and delays footprint reporting and disclosures.

Frequent Formulation changes Slow Reporting

Tap
Granular Reviews expose Credibility Gaps

Clients and investors now demand batch-level data to verify carbon reports. Companies lacking structured ESG data risk credibility loss.

Traceability from Molecule to Batch is now expected

Tap
Solution

Powering the Next Era of Sustainable Pharma

From sourcing to scale-up, track carbon across formulations, facilities, and suppliers. Ensure data stays traceable, audit-ready, and aligned with evolving disclosure norms, without extra workload.

1

Conduct Climate Risk Assessments across your Value Chain

Climate risk in pharma spans physical and transition factors. Mapping flood-prone sites, shifting policies, and investor demands helps build resilience into procurement and supplier planning.

2

Build Supplier-level Visibility for credible Scope 3 data

Pharma supply chains are fragmented. Collecting consistent supplier data on energy, logistics, and materials enables audit-grade Scope 3 calculations and CDP-ready reporting.

3

Create Batch-level Product footprints using Real-world inputs

Accurate LCAs reflect batch-specific process variations. Generating cradle-to-gate data improves product-level reporting and strengthens buyer, regulator, and certification responses.

4

Set Science-Based Targets and Model Reduction Pathways

Switching solvents or improving formulation efficiency affects emissions differently. Scenario modelling aligns actions with SBTi guidance and builds science-based reduction roadmaps.

5

Map disclosures to CDP and Biodiversity-linked frameworks

As reporting expands to water, biodiversity, and supply chain impacts, pharma companies must stay ahead. Structured data aligned to CDP categories improves transparency and speeds up reviews.

HOW IT WORKS

The System behind Smarter Pharma Sustainability

Handling pharma emissions means batch variability, multi-site data, and strict formats. Our system unifies structured collection with intelligence for simpler, credible reporting.

Assess Climate Risks Across Sites and Suppliers

Pharma plants and vendors face rising climate and regulatory exposure. Mapping risks helps teams strengthen planning, procurement, and long-term resilience.

Standardise Supplier Data for Audit-Ready Scope 3

APIs, excipients, and packaging come from suppliers with incomplete reporting. Structured data capture ensures defensible, consistent Scope 3 footprints.

Generate Batch-Specific Product Footprints Easily

Pharma LCAs must reflect real conditions. Capturing batch-level variations ensures accurate cradle-to-gate footprints and stronger compliance responses.

Simulate Reduction Strategies and Set Science-Based Targets

Changing solvents or energy sources alters impact. Scenario modelling helps test interventions and align reduction targets with SBTi guidance.

Align Data with CDP and Biodiversity Frameworks

Disclosures now extend beyond carbon. Structuring environmental data across water, biodiversity, and supply impacts supports faster, transparent reviews.

WHO WE WORK WITH

Working with the Makers of Healthcare

We help pharmaceutical teams build verified, audit-ready sustainability data before it becomes a compliance challenge.

We work closely with:

Drug Discovery Firms: Gain upstream visibility across APIs and intermediates to close Scope 3 gaps and meet investor expectations

Medical Device Manufacturers: Trace emissions across production and operations with verified, compliance-ready data

CDMOs & Contract Partners: Manage multi-client cycles while delivering accurate, consistent sustainability metrics for buyers

For Every step of your Low-Carbon Journey

For your Customers

Pharma buyers and partners now expect verified emissions and batch-level data. Traceable information builds trust in audits, tenders, and supply contracts.

For your Company

Accurate data supports CDP, CSRD, and buyer needs without manual work. It guides sourcing, procurement, and product design decisions internally.

For the Planet

Pharma production drives emissions, water use, and biodiversity impact. Better visibility helps companies act faster and strengthen climate resilience.

WHY KARBONWISE

Because Pharma needs more than Compliance

No more Supplier Blind Spots

From APIs to packaging, gain near-total visibility across upstream vendors. Collect energy, logistics, and process data in audit-ready formats without manual follow-ups.

Reduction Scenarios, Quantified

Deliver disclosures for CDP, CBAM, and CSRD 30% faster. Centralised data access eliminates reformatting delays and ensures every submission is consistent and verified.

100% CDP and Biodiversity Aligned

Map supplier, product, and site-level data directly to CDP indicators and biodiversity-linked metrics, ensuring compliance across global frameworks in one system.

Partner with the Platform for Real Progress

Verify my Pharma Footprint

Frequently Asked Questions