Pharmaceutical products. Product category rules for life cycle assessments. Specification
Pharmaceutical products. Product category rules for life cycle assessments. Specification
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What is PAS 2090:2025 Pharmaceutical products – Product category rules (PCR) for environmental lifecycle assessments – Specification about? PAS 2090 specifies requirements for the product category rules (PCR) to be applied when carrying out an environmental lifecycle assessment (LCA) for pharmaceutical products and for reporting environmental LCA results.
Who is PAS 2090:2025 Pharmaceutical products – Product category rules (PCR) for environmental lifecycle assessments – Specification for? This PAS is intended for use by those carrying out, assessing and reviewing environmental LCAs of pharmaceutical products, including the determination of related greenhouse gas emissions as well as other environmental impacts. This PAS might be of interest to (but is not limited to) the following stakeholders and their representative associations:
Manufacturers of pharmaceutical products and suppliers; Payors and procurement representatives; Environmental managers; Policy setters; Regulators; Healthcare providers; Healthcare professionals; Patients/public; Medicines appraisers; and Researchers and legislators.
NOTE: This PAS is intended to be applicable internationally.
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