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Unlock excellence in clinical research with IAOCR/GCSA certification. This guide answers your questions on the process, value, global alignment, and investment. Become audit-ready and attract top-tier trials.
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Learn about Colombia's new clinical trial bill (Proyecto de Ley 191), filed on August 5, 2025. Discover how this law aims to overhaul outdated 1993 regulations to boost medical research and national competitiveness.
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Enhance patient diversity in clinical trials with effective strategies for inclusive participation.
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Protect your medical device IP in Brazil. This guide explains ANVISA's confidentiality rules, the role of the Brazilian Registration Holder (BRH), and how the Right of Reference (Carta de Autorização) safeguards your technical dossier. Learn to navigate ANVISA and avoid commercial traps.
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Explore the untapped opportunities and challenges in radiopharmaceutical and theranostics clinical trials. This post delves into the complexities of alpha-emitter supply chains, dosimetry, and data management, with a focus on the burgeoning clinical research landscape in Latin America. Gain insights into navigating the regulatory environment in Brazil and Mexico and discover how to optimize your next radiopharmaceutical trial for success.
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Struggling with slow first-in-human trials? This guide shows MedTech founders how to accelerate clinical validation in emerging regions like Latin America for faster approvals and funding.
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Discover why U.S. Medtech startups are forced to conduct First-in-Human trials abroad. Learn about the financial, regulatory, and bureaucratic hurdles in the U.S. and the competitive advantages of global trial destinations. Understand the impact of this "innovation paradox" on U.S. economic leadership and explore policy solutions to strengthen domestic Medtech innovation.
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