Be it prescription or over-the-counter, small molecules or biologics: Medicinal Products is one of the most strictly regulated domains globally. The surge of new and experimental drugs fuelled by changing contexts such as pandemic, demographics, and high-throughput drug discovery methods requires strict vigilance due to their direct impact on human lives.
Biopharma industries need to keep themselves abreast in a timely manner with all the latest regulations: be it guidelines or policies or communications from health authorities- and our Medicinal Products module has been crafted to provide comprehensive regulatory intelligence that keeps patients safe, and your products- compliant.
With an extensive market coverage and diverse sources of information, our early-signalling systems and BOTs capture even the draft regulations so that you can be forearmed and forewarned. With over 1.8 million granular regulatory requirements, 8000 regulatory insights (and counting), you can count on us for everything regulatory.
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Learn how Freyr can help streamline your global regulatory intelligence journey while ensuring that you can craft robust strategies and enable you to achieve your goals quicker.
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