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Esin Kaya
@Esin_Kaya
Joined Jul 10, 2024
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Esin Kaya
@Esin_Kaya
ISO 13485 Certification: Medical Device Quality & Compliance
We have experienced ISO 13485 consultants that can help your medical device manufacturer become compliant with the latest industry standards.ISO 13485 is a quality management system for a medical device manufacturing organization, which is used to control the various processes...
ISO13485
iso13485certification
ISO13485Consultants
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3
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Dec 12, 2024
Esin Kaya
@Esin_Kaya
CE Certification: Contact Lenses Decoded
Explore the intricacies of CE certification for contact lenses. Learn about the standards and processes in this detailed guide. Obtaining CE Certification for contact lenses is not just a regulatory requirement; it’s a strategic investment in the safety, quality, and success o...
CECertificationForContactLenses
CECertification
CEMark
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4
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Dec 4, 2024
Esin Kaya
@Esin_Kaya
MDSAP Certification: Your Key to Global Market Success
Gain global market access with MDSAP Certification, your key to streamlined compliance and international regulatory acceptance. In today’s world, selling your products globally can make your business successful. But, understanding all the rules and regulations in different cou...
MDSAP
MedicalDeviceSingleAuditProgram
MDSAPCertification
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6
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Aug 28, 2024
Esin Kaya
@Esin_Kaya
Symbology for Safety: Enhancing Medical Device Labeling Globally
Dive into global medical device labeling: Symbology for Safety ensures universal understanding across diverse cultures. Explore now! This guideline pertains to symbols employed across various medical devices sold worldwide, necessitating compliance with diverse regulatory stan...
Medicaldevice
MedicalDeviceLabeling
MedicalDeviceSymbols
MedicalDevicePackaging
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5
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Aug 22, 2024
Esin Kaya
@Esin_Kaya
CE Marking for Medical Devices: Europe’s Pathway
Ensure your medical devices meet European standards with CE Marking. Stay compliant and gain market access across the EU. Maven is a regulatory consultancy providing one-stop solution for the CE marking of your medical devices, providing overall support with technical document...
CEMark
CEMarking
CEMarkingMedicalDevices
CEMarkingforMedicalDevices
EuropeanCEMarkingForMedicalDevices
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5
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Aug 7, 2024
Esin Kaya
@Esin_Kaya
Understanding and complying with country registration requirements is essential for successful market entry and ensuring the safety and efficacy of medical devices. Each country may have specific requirements, so it’s essential to consult the respective regulatory authority’s...
CountryRegistration
Medicaldevice
IVDdevices
CountryRegistrationRequirements
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5
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Jul 10, 2024