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EU Cosmetic Ingredient Regulations Exploring the Latest Legislative Updates and Future Restrictions
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Manufacturer’s Challenges: Mastering EU MDR and IVDR Compliance
What Is It All About?
Navigating the Regulatory landscape of the EU MDR and IVDR pose significant challenges for medical device manufacturers. Starting from classification and re-classification to clinical testing requirements, the Notified Bodies (NBs) certification, designating a Person Responsible for Regulatory Compliance (PRRC), and appointing a European Authorized Representative (EAR), every step must be executed diligently. Are you willing to launch your medical device in the EU market?
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Regulatory Landscape of Foods and Health Functional Foods In the South Korean market
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Market Entry for Food Products and Supplements in Latin America: Navigating Regulatory Challenges
Market Entry for Food Products and Supplements in Latin America: Navigating Regulatory Challenges
February 28, 2024
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MDSAP Compliance and Audit Success
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Cosmetics Entry in Nigeria: A Regulatory Roadmap
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Launching Food Supplements in EU Countries – Germany, France, Spain, Italy, and Poland
Launching Food Supplements in EU Countries – Germany, France, Spain, Italy, and Poland
January 24, 2024
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Cosmetics Entry in Nigeria: A Regulatory Roadmap
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Overview of the NDA/BLA Process in South Korea