Resources
Practical insight for
compliance in motion.
Explore Eunomia’s articles, webinars, case studies and working resources — brought together in one place.
Find the right starting point
Which pharma compliance resource do you need?
Use the articles to understand a topic, the worksheets to organise a task and the case studies to see how a defined engagement was delivered. Each serves a different purpose. Adapt working templates to your organisation’s markets, responsibilities and approved procedures.
| Your task | Start here | Practical output |
|---|---|---|
| Plan role-based learning | Training matrix | Topic assignments, learning depth and evidence of application. |
| Assess an HCP fee | FMV assessment worksheet | A record of service need, assumptions and rate rationale. |
| Prepare disclosure data | Disclosure preparation guide | Ownership, reconciliation checks and methodological-note prompts. |
| Improve material review | Promotional review workflow | Submission steps, responsibilities and release controls. |
How should you use the sources?
Read the scope notes alongside each article’s references. An official code or law establishes its own requirements; a worksheet provides a suggested way to organise the work. Check the current source and the relevant national rules before applying guidance to an activity. Case-study outcomes describe specific engagements, rather than results every organisation should expect.
For implementation support, explore programme design and implementation or outsourced compliance operations.
Search articles, webinars, case studies and working resources.
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Featured Content
Role-based pharmaceutical compliance training matrix
Disclosure preparation checklist and methodological-note guide
Pharmaceutical promotional review workflow guide
HCP FMV Assessment Guide and Worksheet
Pharma Compliance Readiness Checklist
EFPIA Code Self-Assessment Checklist
UK & EU Pharma Compliance Guide 2026
EFPIA Disclosure Methodology Note Template
Transparency Disclosure Deadlines by Country
PMCPA Case Library
Pharmaceutical Compliance Glossary
Pharma Compliance Case Studies Pack
Global Healthcare Compliance, Local Disclosure: Navigating Transparency Requirements Across APAC, Spain and Portugal
Materials Review, Shared Service and Streamlined Process
Fair Market Value Methodology
Eunomia perspectives
Articles & insights
38 perspectives on operational compliance, transparency, governance and technology.
EU AI Act Governance & Article 50: A Practical Guide for Pharma
Pharma Compliance Across the Product Lifecycle
The EU AI Act for Pharmaceutical Companies: What Applies and When
Disclosure UK: How It Works, Deadlines, Consent and Objections
EFPIA Disclosure Requirements and Template, Explained
Failure to Prevent Fraud: What Pharmaceutical Companies Need to Do
The ABPI Signatory: Certification Requirements, Role and Training
Lessons from Recent PMCPA Cases: What 2026 Rulings Mean for Your Processes
Managing Healthcare Professionals’ Personal Data under GDPR: CRM, FMV and Engagement Records
GDPR and Transparency Reporting: Disclosing HCP Transfers of Value
How Small and Mid-Sized Pharma Companies Can Build an Effective Compliance Risk Assessment Framework
Top Transparency Reporting Mistakes Pharmaceutical Companies Should Avoid
PMCPA’s 2026 Social Media Guidance: Compliance Priorities Companies Should Address Now
Right-Sized Compliance Support: Meeting the Needs of Both Emerging Biotech and Global Pharma
Navigating Country-Level Accountability in Europe: A Key Pillar of Healthcare Compliance
Scalable Compliance Models for Growing Pharma in the Age of AI
Entering Phase III? Compliance Expectations Already Have
From Risk to Resilience: Why Third-Party Risk Management Is Pharma’s Biggest Competitive Advantage
Compliance Gap Analysis: Reducing Risk Without Slowing Growth
Sunshine Act in France: Understanding the Transparency in Healthcare System
Transparency Reporting in the Pharmaceutical Industry: Legal Compliance Versus Ethical Responsibility
Fair Market Value (FMV) in Healthcare Compliance: Turning Regulatory Expectation into an Operational Capability
Beyond the Checklist: How Gap Analysis Strengthens Healthcare Compliance Internal Audits
Digitalisation in Pharma: Strengthening Healthcare Compliance Through Smart Systems & Integrated Governance
Staying Ahead of the Curve: Audit-Readiness Best Practices Across European Life Sciences Markets
Top 10 Healthcare Compliance Challenges in Pharma Industry and How to Solve Them
What Makes Healthcare Compliance Training Effective?
How to Avoid Common Healthcare Compliance Mistakes in Pharmaceuticals
AI in Healthcare Compliance: Navigating Opportunities, Risks, and Regulatory Landscapes
Compliance Training: Beyond the Code
A Definitive Guide to Crafting a high-quality Policy for a Pharmaceutical Company
Stakeholder Engagement vs Risk: EFPIA & IFPMA Compliance
Risk Assessment in Healthcare and its Importance
The Future of Diversity & Inclusion in Pharma Compliance: A European Perspective
Unleash the Power of Data Analytics for Healthcare Compliance
Importance of Bespoke Healthcare Compliance Training for Pharmaceutical Industry
Managing compliance Risks: Best Practices & Strategies
Staying Ahead in Healthcare Compliance: Navigating AI Challenges with Ethical Governance
Questions, answered
About our resources
Are the resources free?
Yes. Articles and case studies are free to read. The practical Excel worksheets can be downloaded directly. Some PDF checklists and guides use a request form so we can send the file.
How are the articles sourced?
Each article opens with a short answer and ends with its sources. Legal and code statements link to the official text, such as EUR-Lex, legislation.gov.uk, the PMCPA or EFPIA.
Are these resources legal advice?
No. They are practical, informational guidance. Requirements depend on your organisation, markets and activities, and should be confirmed for your situation.
Where can I find country-specific rules?
Our country guides cover Germany, France, Spain, Italy, the Netherlands, Portugal, Ireland and Sweden, each with links to official sources. They are listed on the Legal Mandates page.