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Plan for the development of clinical trials in Poland until 2030

Publication date: March 11, 2026

Clinical trials in Poland – status as of 2025

Clinical trials in Poland have developed significantly over the past 30 years. In 2024, Poland ranked 9th in the global commercial clinical trials market, translating into a 2.68% market share. These high results have allowed Poland to create approximately 9,400 jobs and provide 26,800 patients with access to innovative and cutting-edge experimental therapies. The medical research industry in Poland is growing rapidly, making it an attractive investment destination. According to the report, the world’s largest industry sponsors are the dominant sponsors in Poland. They account for 43% of all active industry-run research centers worldwide and 47% of active centers in Poland. This demonstrates Poland’s strong integration with global clinical trial networks. It is important to note that Poland’s growth in the clinical trials sector occurred after the challenging pandemic years. Due to the epidemiological threat and mobility restrictions imposed by the pandemic, the development of commercial clinical trials has been hampered. These were replaced by research on the SARS-COV-2 disease, as there was an urgent need to study the new disease and develop a treatment due to the global COVID-19 pandemic. Despite the pandemic and the increased attention focused on researching the new virus, Poland has not completely abandoned the development of clinical trials, as evidenced by the Polish Clinical Trials Network.

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European Defence Cooperation Strengthened at E5 Summit in Kraków; Joint Initiative on Drones and Air Defence Announced –  In the background of the photo – the office of KG LEGAL Kiełtyka Gładkowski law firm

Publication date: February 26, 2026

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Act on the Financial Instrument for Increasing Safety SAFE – systemic and legal-financial analysis

Publication date: February 26, 2026

Introduction

The Act of 13 February 2026 on the SAFE Financial Instrument for Enhancing Security is the national legislature’s response to the European Union’s establishment of a new financial mechanism aimed at strengthening the defense capabilities of Member States. The SAFE Instrument (Strategic Technologies for Europe Platform) was established pursuant to a regulation of the Council of the European Union of 27 May 2025 as an emergency measure to accelerate investment in the European defense industry and increase the interoperability and readiness of the armed forces of EU Member States.

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AI Cartels

Publication date: February 26, 2026

Pricing API language models, collaboratively restricting access to the most advanced models, blocking interoperability, collaborative lobbying for regulations that hinder startup entry – is market ready for this?

An AI cartel is a situation in which AI-developing companies secretly or openly cooperate in a way that restricts competition—for example, by fixing prices, blocking access to technology, or jointly eliminating smaller players from the market.

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10 principles of good practice in the application of AI in the drug life cycle

Publication date: February 25, 2026

Slide 1 – title: introduction

We are facing changes: AI in the pharmaceutical industry is no longer a foreign concept. It means shorter trials, more accurate diagnoses, and the potential for drugs where we previously had given up hope. But let’s be honest, technology without a roadmap is risky. That’s why the EMA and FDA sat down to create a ten-page guide to “good practice.” These aren’t rigid rules, but a foundation of trust. We can encapsulate these 10 principles in three logical pillars.

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