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Biotech companies are at the forefront of innovation, but many operate with small teams, limited resources, and budgets that must be stretched carefully across clinical and regulatory priorities. Despite these constraints, the demands around multilingual documentation are as strict as in large pharma. Regulatory authorities expect accuracy, consistency, and compliance — and even a small […]
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Gestionar contenido multilingüe, ya sean IFUs, empaques o documentación regulatoria, no tiene por qué ser abrumador. Aun así, muchas empresas de dispositivos médicos enfrentan presiones de último minuto antes de auditorías, lanzamientos de productos o presentaciones regulatorias. ¿La ventaja? Con el marco adecuado, las actualizaciones pueden completarse de forma rápida, rentable y totalmente conforme. Aquí […]
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Managing multilingual content, whether it’s IFUs, packaging, or regulatory documentation. doesn’t have to be overwhelming. Still, many medical device companies face last-minute pressure before audits, product launches, or regulatory submissions. The advantage? With the right framework, updates can be completed quickly, cost-effectively, and in full compliance. Here’s how to make multilingual updates an integrated and […]
