Inovação e gerenciamento de programa sincronizado e colaborativo para novos programas
Aeroespacial e Defesa
Inovação e gerenciamento de programa sincronizado e colaborativo para novos programas
Explorar o SetorAutomotivo e Transporte
Integration of mechanical, software and electronic systems technologies for vehicle systems
Explorar o SetorProdutos de Consumo e Varejo
A inovação de produtos através do gerenciamento eficaz de formulações, embalagens e processos de manufatura integrados
Explore o SetorEletrônicos e Semicondutores
O desenvolvimento de novos produtos aproveita dados para melhorar a qualidade e a lucratividade e reduz custos e tempo de introdução no mercado
Explore o SetorEnergia e Utilidades
Supply chain collaboration in design, construction, maintenance and retirement of mission-critical assets
Explorar o SetorHeavy Equipment
Construction, mining, and agricultural heavy equipment manufacturers striving for superior performance
Explore IndustryMáquinas Industriais e Equipamento Pesado
Integration of manufacturing process planning with design and engineering for today’s machine complexity
Explorar o SetorInsurance & Financial
Visibility, compliance and accountability for insurance and financial industries
Explore IndustryMarinha
Inovação na construção naval para reduzir de maneira sustentável o custo do desenvolvimento de frotas futuras
Explore o SetorMedia & Telecommunications
Siemens PLM Software, a leader in media and telecommunications software, delivers digital solutions for cutting-edge technology supporting complex products in a rapidly changing market.
Explore IndustryDispositivos Médicos e Farmacêuticos
“Inovação de produtos personalizados" através da digitalização para atender a demandas do mercado e reduzir custos
Explore o SetorSmall & Medium Business
Remove barriers and grow while maintaining your bottom line. We’re democratizing the most robust digital twins for your small and medium businesses.
Explore IndustryOperational Excellence for MedTech
Operational Excellence for MedTech
Learn valuable insights from the FDA on the use of automation, information technology, and data solutions throughout the product lifecycle.
Digitalization in manufacturing brings FDA and medical device and diagnostic firms together. The use of automation, information technology, and data solutions throughout the production process provides manufacturers advantages for minimizing errors, accelerating regulatory processes, increasing business value, optimizing resources, and reducing patient risk.
Register for our webinar and hear straight from the FDA and W.L. Gore what digitalization means for manufacturing product quality excellence. Learn valuable insights from the FDA about how they are shifting the perception of the agency of being a regulated space and its openness to collaboration with the manufacturing industry on the use of automation, information technology, and data solutions throughout the product lifecycle.
The FDA’s focus has always been on consumer safety, product efficacy, and regulatory compliance. The challenges that can occur in this space include a focus on meeting regulatory requirements versus adopting best quality practices. The agency sees the need to shift into operational excellence for MedTech through digitalization as a way to bring speed, control, and agility to its approach. Adopting this way of thinking will achieve quicker product innovation while maintaining product quality. The FDA sees the need to drive connections within quality systems to enable simplification, error-proofing, and a culture of rapid learning and continuous improvement. Their readiness to unleash innovation and improvements will be explored more thoroughly during this webinar hosted by Siemens.
Medical device companies realize that smart manufacturing is the fastest way to achieve operational excellence in today’s global marketplace. With current world conditions adversely impacting markets and exerting unprecedented pressures on medical device manufacturers, the journey towards smart manufacturing is essential to remain competitive. Accelerating product innovation while at the same time controlling product performance has never been more important. MedTech automation allows you to be connected so you can get real-time data to see how things are shifting and performing – allowing for direct visibility to address problems immediately and continuously improve design. Adopting digitalization improves analytics and fosters error-proofing and paperless manufacturing. The end result is quality and responsiveness to issues, enabling a true total product lifecycle approach that improves the effectiveness and efficiency in the medical device community.
The current use of paper-based processes in manufacturing increases the risk of poor quality, delays in time to market and higher costs. It will become increasingly challenging to keep pace with today's efficiency standards – let alone improve them – while maintaining compliance and safety. Industry leaders have evolved and implemented systems to automate manufacturing execution and manage data related to manufacturing processes as an electronic DHR (eDHR). Others have not yet evolved and are still using paper-based processes. As a result, they face challenges in scaling these systems, especially across globally distributed production facilities and when contracting with manufacturing partners. Join this webinar to grow your understanding of how moving away from paper into a virtualized data can open us up to what is most relevant and important in a traceable connected record.
You will learn:
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Learn valuable insights from the FDA on the use of automation, information technology, and data solutions throughout the product lifecycle.
Digitalization in manufacturing brings FDA and medical device and diagnostic firms together. The use of automation, information technology, and data solutions throughout the production process provides manufacturers advantages for minimizing errors, accelerating regulatory processes, increasing business value, optimizing resources, and reducing patient risk.
Register for our webinar and hear straight from the FDA and W.L. Gore what digitalization means for manufacturing product quality excellence. Learn valuable insights from the FDA about how they are shifting the perception of the agency of being a regulated space and its openness to collaboration with the manufacturing industry on the use of automation, information technology, and data solutions throughout the product lifecycle.
The FDA’s focus has always been on consumer safety, product efficacy, and regulatory compliance. The challenges that can occur in this space include a focus on meeting regulatory requirements versus adopting best quality practices. The agency sees the need to shift into operational excellence for MedTech through digitalization as a way to bring speed, control, and agility to its approach. Adopting this way of thinking will achieve quicker product innovation while maintaining product quality. The FDA sees the need to drive connections within quality systems to enable simplification, error-proofing, and a culture of rapid learning and continuous improvement. Their readiness to unleash innovation and improvements will be explored more thoroughly during this webinar hosted by Siemens.
Medical device companies realize that smart manufacturing is the fastest way to achieve operational excellence in today’s global marketplace. With current world conditions adversely impacting markets and exerting unprecedented pressures on medical device manufacturers, the journey towards smart manufacturing is essential to remain competitive. Accelerating product innovation while at the same time controlling product performance has never been more important. MedTech automation allows you to be connected so you can get real-time data to see how things are shifting and performing – allowing for direct visibility to address problems immediately and continuously improve design. Adopting digitalization improves analytics and fosters error-proofing and paperless manufacturing. The end result is quality and responsiveness to issues, enabling a true total product lifecycle approach that improves the effectiveness and efficiency in the medical device community.
The current use of paper-based processes in manufacturing increases the risk of poor quality, delays in time to market and higher costs. It will become increasingly challenging to keep pace with today's efficiency standards – let alone improve them – while maintaining compliance and safety. Industry leaders have evolved and implemented systems to automate manufacturing execution and manage data related to manufacturing processes as an electronic DHR (eDHR). Others have not yet evolved and are still using paper-based processes. As a result, they face challenges in scaling these systems, especially across globally distributed production facilities and when contracting with manufacturing partners. Join this webinar to grow your understanding of how moving away from paper into a virtualized data can open us up to what is most relevant and important in a traceable connected record.
You will learn: