
Sector
Carbon footprint, water footprint, waste, and supply chain in an enterprise platform. Traceable, organized for review, and built for the demands of the healthcare sector.

Managed climate impact
kg CO₂e
−12% year on year
All scopes in one dashboard
According to Health Care Without Harm, the health sector accounts for around 4.4% of global net emissions. Regulatory pressure, the requirements of large hospital groups, and ESG investor demands make environmental management a strategic priority.
Healthcare waste is highly regulated. Traceability from generation to the final handler is a legal obligation and an operational risk if not managed well.
Scope 3 of a pharmaceutical company or medical device manufacturer includes raw materials, active ingredients, packaging, and global distribution. Measuring it requires specific tools.
Large hospital groups and public administrations are incorporating sustainability criteria into their tenders. Suppliers without data are at a disadvantage.
Classification by LER code, documentation of handlers and transfers, generation of reports for authorities. Less reliance on spreadsheets and clearer evidence for compliance reviews.
LCA of pharmaceutical products and medical devices. Breakdown by raw material, manufacturing process, and distribution. Data structured to help you prepare for Digital Product Passport requirements.
Automated surveys to ingredient, packaging, and logistics suppliers. Assessment of their environmental performance and AI-generated improvement plans.
Auditable reports with full traceability. Workflows for CSRD, ISO 14064, and ESG reports for private equity and pharmaceutical funds.
GHG Protocol · ISO 14064 · ISO 14067 · CSRD (ESRS E1, E5) · CSDDD · Royal Decree 214/2025 (MITECO) · Law 7/2022 on Waste · Digital Product Passport · EU Taxonomy · GRI 306
Talk to our team and discover how pharmaceutical and healthcare companies already manage their impact with Manglai.
Key Features
Bring facility energy, water, materials, product and waste data into one workspace so environmental and quality teams can follow operational and value-chain impacts.
Structure laboratories, manufacturing sites, legal entities and business units so local EHS owners, quality teams and corporate sustainability staff can manage their responsibilities.
70 employees
ES
Complex Hierarchies
Unlimited Users
Bring process energy, active ingredients, packaging purchases, distribution information and waste records together, with source documents available for review.




























































































































































Integrations
Bulk Import
Task Management
Review how ingredients, packaging, production energy and distribution data contribute to product or corporate impact figures, with factors and calculation history visible.
Updated Factors
Calculation traceability
Quality control
Share traceable data with hospital procurement teams, healthcare groups and investors, while keeping the evidence behind facility, product and supplier figures available for review.
Traceable reports
Manglai experts can help environmental, procurement and quality teams refine boundaries and prepare evidence while suppliers and manufacturing sites provide their records.
Expert guidance
Set access by site, business unit and role, with secure sessions and single sign-on for manufacturing, ingredient and supplier information.

Data encryption
GDPR Compliance
International standards
Our clients
Discover how companies in various sectors are already operating their environmental management with Manglai

We backed their vision, and all we can say is that we'll keep working with them. Week after week, they bring us small improvements that make their product stronger from a user's perspective.
Carla Argiles
Quality and Environmental Technician - Sertrans
We're very happy with the platform and the service provided by the Manglai team. Thank you very much!
Vesselin Petrov
ESG Coordinator - Bluespace









Regulatory compliance
Decide which labs, production sites, product families, ingredients, packaging and transport stages belong in each assessment, and note the reporting periods and data sources.
Separate product and corporate inventories
List ingredient, packaging and process data
Track supplier evidence by product