Orliman
Laura M is an experienced professional in regulatory affairs and quality management, currently serving as Responsable Regulatory Affairs at Orliman since May 2022. Prior to this role, Laura worked as a Quality Technician at TEQUIR I+D+i and held the position of Responsable Técnico/Calidad y Asuntos Regulatorios at Laboratorios Herbitas. Laura's extensive background includes responsibilities in quality system maintenance, ISO 13485 audits, and communication with regulatory agencies. Additionally, Laura has experience in pharmacovigilance and has held various pharmacist roles in multiple pharmacies. Educational qualifications include a Licenciatura in Pharmacy from Universidad de Farmacia, a Master's in Clinical Trials Management, and numerous certifications related to quality and pharmacological practices.
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Orliman
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Orliman started as a family orthopedic business more than 70 years ago. The Orliman, limited society was established in the last decade for development and mass production of orthopedic products. The company´s strategy is based on constant research of new products, the quality and performance of these products and a personalized service and attention to the customer is maximized by an ongoing assessment of the customer´s and market needs. We are the first Spanish company in the sector with a completely automatic storage and distribution system. Sobre Orliman Orliman tiene sus orígenes en un negocio familiar de ortopedia con más de 70 años de historia, creando en la última década la sociedad Orliman, S. L. U. para el desarrollo y fabricación de productos ortopédicos en serie. Su estrategia empresarial está basada en la constante investigación de nuevos productos, la calidad y prestaciones de los mismos y un servicio y atención personalizado al cliente, con una permanente interpretación de sus necesidades y las del mercado. Primera empresa española de su sector con un sistema de almacenaje y distribución totalmente robotizado.