In the rapidly evolving world of personalized medical devices, ensuring consistent quality is not just important—it’s paramount. As Ketan Jajal, CEO of 3d surgical, emphasized in our recent webinar. From regulatory frameworks like FDA and TGA to process validations, scaling personalized devices hinges on quality systems, proper communication, and robust platforms. Let us know in the comments how your organization prioritizes quality in personalized devices. #InnovationInHealthcare #3DMedicalDevices #QualityMatters #ProcessValidation #RegulatoryExcellence
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Managing Director, Healthcare Risk Management & Advisory | Coding and Billing | Investigations, Disputes and Compliance
In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/g3Fym4dH
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/e4NXKsS3
Crucial Role of Mock Recalls Medical Device Industry | FTI
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/dcqUWwaX
Crucial Role of Mock Recalls Medical Device Industry | FTI
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/gHVFSDVx
Crucial Role of Mock Recalls Medical Device Industry | FTI
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/es2VANtU
Crucial Role of Mock Recalls Medical Device Industry | FTI
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/gYJ4e59F
Crucial Role of Mock Recalls Medical Device Industry | FTI
fticonsulting.social
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/eN8DiKkR
Crucial Role of Mock Recalls Medical Device Industry | FTI
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Digital Health Executive | Managing Director | Strategic Advisor | Innovator | unlocking revenue and reducing costs: Implementing innovative, data-backed IT strategies for a strong ROI
In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/gwj6uVP8
Crucial Role of Mock Recalls Medical Device Industry | FTI
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In 2023, the FDA reported 975 recalls for medical devices, affecting everything from simple instruments to complex implantable devices. A recall can tarnish brand credibility, constrain healthcare providers, and compromise patient health and safety. Our experts walk through the key advantages of integrating mock recalls to optimize recall execution: https://lnkd.in/eBHmJAzr
Crucial Role of Mock Recalls Medical Device Industry | FTI
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💡 Master UDI-DI: A Key Guide for the Contact Lens Industry The Medical Device Coordination Group (MDCG) has released a crucial document: MDCG 2024-14 Guidance on Master UDI-DI for contact lenses. This guidance provides practical insights into implementing the Master UDI-DI system, enhancing identification and traceability of medical devices. Key Information: The Master UDI-DI is designed for highly personalized devices, such as contact lenses. Clear rules for assignment, labeling, and registration in the Eudamed database. Compliance becomes mandatory in 2025, but early implementation is encouraged. An essential step to improve transparency and safety across the industry. If you’re a manufacturer or economic operator and have questions about compliance, we’re here to help. Read the more detailed article on our website at cmcmedicaldevices.com in the News section. #UDI #MedicalDevices #ContactLenses #Regulations #Eudamed #MasterUDIDI #Compliance #HealthcareInnovation
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Winner Of ET NOW Leaders Of Tomorrow Founder & CEO at Orthotech India Pvt Ltd
5dGood Mr.Jajal...for raking up this issue, This is really important, as we see Multiple metal printers installed for various other applications other than Medical applications are printing implants...it's a very serious issue...considering the impurity,validation, cleanliness, traceability, many such important aspects related to medical devices are overlooked, company like ours who are there for 25yrs with all the regulatory approvals for class 3 devices, have to compete with one machine sheds,for all applications. Hope,we see major improvement in the regulatory for Patient Specific Implants.