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Expertos en normativa europea
LLleva tu producto al mercado con confianza con la ayuda de nuestros expertos en Regulatory Affairs. Desde planificar la estrategia hasta conseguir la aprobación de tu producto, estamos aquí para ofrecerte un servicio personalizado que te ayudará a navegar por los requisitos más complejos y cumplir con los estándares de la UE.
Experiencia
Profesionales experimentados con un profundo conocimiento del panorama normativo y de los retos a los que se enfrentan los fabricantes.
A medida
Adaptamos nuestros servicios a las necesidades específicas de cada cliente, garantizando un enfoque a medida para tu proyecto.
Siempre al día
Al día de las normas, directrices y mejores prácticas del sector, para garantizar que tu documentación cumple las normativas más recientes.
Experiencia sobre el terreno
Consultores con amplia experiencia sobre el terreno, incluidas presentaciones electrónicas.
Tendencias y retos del mercado
Las tecnologías emergentes y los productos innovadores, como las terapias combinadas y los dispositivos médicos, añaden aún más complejidad a los procesos regulatorios. Navegar por estas complejidades requiere experiencia especializada y un enfoque proactivo para garantizar aprobaciones a tiempo.
La globalización también aumenta los desafíos regulatorios, ya que las empresas deben gestionar el cumplimiento en múltiples mercados. Un enfoque estratégico y unificado en Regulatory Affairs es fundamental para mantenerse competitivo y cumplir con la normativa.
Los expertos en Regulatory Affairs de QbD Group te ofrecen la visión y el apoyo necesarios para enfrentar estos desafíos de manera efectiva, asegurando el cumplimiento y permitiéndote llevar tus productos al mercado sin demoras.
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Servicios de Regulatory Affairs para
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![Drug Development](https://www.qbdgroup.com/hubfs/Imported_Blog_Media/regulatory-affairs-900x601.jpg)
![Early Development](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(1).png)
![Scientific Advice](https://www.qbdgroup.com/hubfs/AI-Generated%20Media/Images/medical%20device.jpeg)
![Regulatory Procedures](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(13).jpg)
![Submissions](https://www.qbdgroup.com/hubfs/Hero%20image%20(14).jpg)
![eCTD Publishing](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(15).jpg)
![Artwork & Labeling](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(16).jpg)
![Lifecycle Management](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(17).jpg)
![Combination Products](https://www.qbdgroup.com/hubfs/Webinar%20-%20Drug-Device%20Combination%20Products%20and%20Article%20117%20-%20QbD%20Group.jpg)
![Information Officer](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(19).jpg)
![Orphan Diseases](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(20).jpg)
![Regulatory Intelligence](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(21).jpg)
![RA Strategy for MD & IVD](https://www.qbdgroup.com/hubfs/AI-Generated%20Media/Images/writing%20document.jpeg)
![RA Design & Development](https://www.qbdgroup.com/hubfs/RA%20Design%20%26%20Development%20-%20Regulatory%20Affairs%20-%20QbD%20Group.jpg)
![Legal Representative](https://www.qbdgroup.com/hubfs/Legal%20Representative%20-%20Regulatory%20Affairs%20-%20QbD%20Group%20(4).jpg)
![Technical Documentation](https://www.qbdgroup.com/hubfs/Technical%20Documentation%20-%20Regulatory%20Affairs%20-%20QbD%20Group.jpg)
![Notified Body Submissions](https://www.qbdgroup.com/hubfs/Notified%20Body%20Submission%20-%20Regulatory%20Affairs%20-%20QbD%20Group.jpg)
![Post-Market Surveillance](https://www.qbdgroup.com/hubfs/PMS%20-%20Regulatory%20Affairs%20-%20QbD%20Group.jpg)
![In-country Representative Services](https://www.qbdgroup.com/hubfs/In-country%20Representative%20service%20-%20Regulatory%20Affairs%20-%20QbD%20Group.jpg)
![Person Responsible for Regulatory Compliance (PRRC)](https://www.qbdgroup.com/hubfs/Clinical%20Quality%20Services%20-%20Clinical%20-%20QbD%20Group.jpg)
![Authorized Representative (EC-REP)](https://www.qbdgroup.com/hubfs/Authorized-Representative-EC-REP-Quality-by-Design.jpg)
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![UK Responsible Person (UKRP)](https://www.qbdgroup.com/hubfs/UK-Responsible-Person-UKRP-Quality-by-Design.jpg)
¿Por qué QbD Group?
En QbD Group, no solo entendemos los desafíos regulatorios, sino que los resolvemos. Con más de una década de experiencia, una red global y un equipo de más de 600 expertos, ofrecemos soporte integral para todas tus necesidades en Regulatory Affairs.
¿Qué nos diferencia?
- Expertise especializado: Conocimiento profundo de los marcos regulatorios de la UE y globales.
- Estrategias personalizadas: Enfoques hechos a medida que se adaptan a tu producto y mercado.
- Alcance global: Perspectivas locales con escalabilidad internacional.
- Actualizaciones proactivas: Siempre al tanto de los cambios regulatorios para asegurar la conformidad.
Trabaja con QbD Group para simplificar los procesos de cumplimiento y acelerar tu camino hacia el éxito en el mercado.
¿Necesitas apoyo? No dudes en contactarnos.
Más de 10 años de experiencia
Asistencia durante todo el ciclo de vida
Presencia mundial
Empresa mejor gestionada
Nuestras ofertas para Asuntos Reglamentarios en
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![Certified PV Audits, Mock Inspections & Activities ISO](https://www.qbdgroup.com/hubfs/Certified%20PV%20Audits%20Mock%20Inspections%20and%20ISO%20Activities%20-%20Vigilance%20-%20QbD%20Group.jpg)
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![Literature Monitoring Search Solutions & Alerts and a Set of Medical Information Solutions](https://www.qbdgroup.com/hubfs/Literature%20Monitoring%20Services%20-%20Vigilance%20-%20QbD%20Group%20(1).jpg)
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![Annual Product Review (APR) & Product Quality Review (PQR)](https://www.qbdgroup.com/hubfs/Annual%20Product%20Review%20(APR)%20%26%20Product%20Quality%20Review%20(PQR)%20%20QbD%20group.jpg)
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![Scientific Advice](https://www.qbdgroup.com/hubfs/AI-Generated%20Media/Images/medical%20device.jpeg)
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![Combination Products](https://www.qbdgroup.com/hubfs/Webinar%20-%20Drug-Device%20Combination%20Products%20and%20Article%20117%20-%20QbD%20Group.jpg)
![Information Officer](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(19).jpg)
![Orphan Diseases](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(20).jpg)
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Contacta con nosotros
Afrontar entornos regulatorios complejos puede ser un desafío, pero no tienes que enfrentarlo solo. Nuestro equipo de expertos te acompañará en cada etapa del proceso.
Contáctanos hoy mismo y trabajemos juntos para garantizar que tus productos cumplan con las normativas internacionales.
Recursos
![preview_image](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Hero%20image%20(3).png)
![preview_image](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Guiding-Glioblastoma-Research-to-the-Clinic-with-Precision-Business-Planning_-1-768x768.jpg)
Guiar la investigación del glioblastoma de la Universidad Católica de Lovaina hacia la clínica con una planificación empresarial precisa
![preview_image](https://www.qbdgroup.com/hubfs/AI-Generated%20Media/Images/scientists%20microscope.jpeg)
![preview_image](https://www.qbdgroup.com/hubfs/Website%202025%20-%20Pictures/Case%20Study%20-%20New%20Hemophilia%20Drug%20Line%20for%20Large%20Biotech.jpg)