Onshoring vs. Offshoring: Rethinking Pharma Manufacturing Post-COVID
The COVID-19 pandemic shattered the illusion of global supply chain invincibility. As pharmaceutical companies scrambled to secure active pharmaceutical ingredients (APIs), packaging materials, and personal protective equipment, it became glaringly evident that a dependency on

The COVID-19 pandemic shattered the illusion of global supply chain invincibility. As pharmaceutical companies scrambled to secure active pharmaceutical ingredients (APIs), packaging materials, and personal protective equipment, it became glaringly evident that a dependency on distant offshore facilities posed a critical vulnerability. In response, the pharma industry is now undergoing a fundamental strategic reassessment: should manufacturing remain offshore for cost advantages, or is it time to bring operations back home through onshoring?
The Case for Offshoring: Efficiency at a Cost
Historically, pharmaceutical manufacturers have embraced offshoring to reduce production costs, gain access to skilled labor, and scale rapidly. Countries such as India and China have become global hubs for API production, driven by favorable labor economics and lenient regulatory environments. Offshore facilities have allowed companies to remain competitive in pricing and have supported global drug accessibility.
However, the pandemic exposed the risks of this model. Border closures, shipping delays, and export bans crippled supply chains. In particular, countries that relied heavily on foreign APIs struggled to maintain consistent drug availability. The result was a wake-up call: cost-saving strategies must now be weighed against the risk of supply disruption.
The Onshoring Renaissance: Resilience Over Cost
Onshoring—relocating manufacturing back to domestic markets—is gaining momentum as a strategy to build resilience and national self-reliance. Governments are supporting this shift through incentives, subsidies, and public-private partnerships aimed at strengthening local pharmaceutical infrastructure.
For instance, in the United States and parts of Europe, initiatives are underway to fund domestic API and vaccine production facilities. The goal is to reduce dependency on foreign suppliers and enhance preparedness for future health crises.
The benefits of onshoring include:
- Greater control over quality and compliance with stringent regulatory standards.
- Reduced logistical risks and shorter lead times.
- Enhanced responsiveness to emergencies and national security threats.
- Support for local economies and job creation.
That said, onshoring also comes with increased operational costs and longer timelines for facility setup and workforce training. It may be more suited for essential and high-value drugs, where supply assurance outweighs price sensitivity.
Hybrid Models and Strategic Flexibility
Rather than an either-or approach, many pharma companies are now exploring hybrid manufacturing models. This strategy involves:
- Maintaining core production capabilities domestically for critical drugs.
- Leveraging offshore partners for volume production or non-essential drug components.
- Implementing digital technologies like AI-driven demand forecasting and blockchain for transparent supply chain management.
Such diversification helps mitigate risk without completely abandoning the cost advantages of offshoring.
Policy and Collaboration: The Role of Governments
The future of pharma manufacturing also hinges on proactive government policies. To support onshoring, regulatory agencies must streamline approval processes for new facilities and create clear frameworks for quality assurance. Meanwhile, international cooperation remains crucial to address shared challenges like raw material shortages and regulatory harmonization.
Strategic Rethinking is Non-Negotiable
The post-COVID world demands a pharma manufacturing model that balances resilience, cost-efficiency, and global equity. Onshoring offers a path toward greater autonomy and reliability, while offshoring remains integral for global scalability and affordability. Ultimately, a flexible, risk-aware strategy—anchored in both national interest and global cooperation—will define the next era of pharmaceutical manufacturing.
As the industry adapts to new realities, the companies that thrive will be those that prioritize agility over tradition and resilience over short-term gains.