Whitepapers & Technical Reports
In-depth expert papers on pharma serialization, Digital Product Passport, anti-counterfeiting and modern track & trace technologies — authored by SeriSoft experts.
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6
Expert Reports
6
Whitepapers
5
Topic Areas
DE/EN
Languages
100%
Free
Key Topics
EU FMD & US DSCSA: The Complete Pharma Serialization Compliance Guide 2025
Comprehensive guide covering EU Falsified Medicines Directive and US Drug Supply Chain Security Act. Includes step-by-step implementation checklists, NMVS integration guides, and a readiness assessment framework for pharmaceutical manufacturers of all sizes.
28
Pages
DE / EN
Language
Format
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Digital Product Passport: ESPR Implementation Roadmap 2026–2030
Authoritative guide to the EU ESPR regulation and DPP requirements. Covers mandatory product categories, data attribute standards, QR code specs, and the phased rollout timeline from batteries (2026) through textiles (2030).
DownloadAnti-Counterfeiting in the Digital Age: Protecting Brands & Patients
In-depth analysis of modern anti-counterfeiting technologies combining physical security features with digital authentication.
DownloadTrack & Trace ROI: Building the Business Case for Serialization
Data-driven business case framework for pharma and consumer goods companies. Quantifies direct ROI from recall cost reduction (avg. 23%), counterfeit loss prevention, and operational efficiency gains.
DownloadGS1 Standards in Pharmaceutical Supply Chains: A Practical Guide
Practical guide to implementing GS1 standards in pharmaceutical track & trace: GS1-128 barcodes, DataMatrix codes, SGTIN, SSCC, GLN identifiers and EPCIS event reporting.
DownloadSerialization Technology Landscape: Evaluation Framework for Pharma Manufacturers
Independent analysis of serialization technology platforms, deployment models (on-premise, cloud, hybrid), and integration complexity.
DownloadRequest a Custom Report
Need an in-depth analysis on a specific compliance topic, technology, or market? Our experts create tailored reports designed precisely for your requirements.
- Tailored to your industry & regulatory environment
- Authored by certified track & trace experts
- Available in German and English
- Typically delivered within 2–3 weeks
Compliance Analysis
FMD, DSCSA, ESPR, GMP
Technology Comparisons
Platforms & vendors
Market Intelligence
Regulatory landscape
ROI Calculations
Business case templates
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