Few industries face such a complex and constantly evolving regulatory landscape, with strict laws applying to multiple aspects of production, supply, and marketing.
In an industry where trust is paramount, demonstrating a commitment to regulatory compliance through advanced packaging and supply chain management can be a powerful differentiator. It not only ensures legal and ethical operations but also contributes to a more trustworthy pharmaceutical sector.
In this blog, we will explore how pharmaceutical packaging can simplify regulatory risk management and support compliance. Discover the complex web of pharmaceutical regulations and learn about the critical role of pharmaceutical packaging today.
The regulatory landscape of pharmaceuticals
The pharmaceutical industry is overseen by various governmental and industry bodies, each with its own set of rules and accountability processes. In the UK, the Medicines and Healthcare products Regulatory Agency (MHRA) take the lead, whilst the United States rely on the Food and Drug Administration (FDA), and the European Union is governed by the European Medicines Agency (EMA).
Industry bodies also play a crucial role in maintaining standards:
- International Federation of Pharmaceutical Manufacturers & Associations (IFPMA)
- European Federation of Pharmaceutical Industries and Associations (EFPIA)
- China Pharmaceutical Industry Association (CPIA)
- Pharmaceutical Research and Manufacturers of America (PhRMA)
These organisations have the authority to sanction companies that breach their codes of practice.
While each region’s regulations may differ, the relevant aspects of compliance in the pharmaceutical supply chain follow a general pattern of:
- Trackability, with end-to-end visibility
- Record-keeping and data collection (now expected to be digital at every stage)
- Accountability and named signatories
- Security and quality control measures