PPWR Readiness Assessment for Pharma Packaging

PPWR Readiness Assessment for Pharma Packaging
Product Description

Regulation (EU) 2025/40 (PPWR) has applied across the EU-27 since 12 August 2026. For pharma the exposure is uneven: primary packaging of medicinal products is exempt from the recyclability and recycled-content targets — but that exemption has to be documented, and secondary, transport and e-commerce packaging are fully in scope, along with harmonised labelling and eco-modulated EPR fees.

We map your portfolio against every PPWR obligation and its effective date, then deliver a per-SKU compliance status, a prioritised remediation roadmap with cost impact, and an audit-ready evidence file.

Four modules, available together or individually.

Positive Organizations

  • Country/Region:
    Switzerland
  • On CPHI since:
    2026
  • Certificates:
    1
  • Employees:
    1 - 24
Company types
Consultancy
Primary activities
Other
Regulatory Affairs
Specifications
  • Details
    1. Labelling — migrate national disposal schemes (Italian, French) to harmonised EU material and sorting labels with QR, due 12 August 2028.

    2. Recycled content — verify traceable supplier certificates (RecyClass, ISCC PLUS) against the 2030 PCR targets; document derogations so they survive audit.

    3. Recyclability — confirm materials are actually recycled at scale in Europe; per-SKU replacement plan before 2030.

    4. Void space — volumetric proof against the 50% empty-space limit (2030), audit-ready per pack format.

    FOR: pharma and generic manufacturers, CDMOs, contract packagers, medical device and IVD makers, packaging suppliers. Covers secondary, transport and e-commerce packs.
  • Selling Points
    Packaging; Sustainability
  • Model
    Four-module assessment · remote or on-site · EU-27 scope
  • Supplied from
    Switzerland

Positive Organizations

  • Country/Region:
    Switzerland
  • On CPHI since:
    2026
  • Certificates:
    1
  • Employees:
    1 - 24
Company types
Consultancy
Primary activities
Other
Regulatory Affairs

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