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IVDR's Summary of Safety and Performance: Your Essential GuiIVDR's Summary of Safety and Performance: Your Essential Gui

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Delve into IVDR's Summary of Safety and Performance for crucial insights and compliance essential...

Khám Phá Cuộc Phiêu Lưu cùng Suzuki Jimny tại Việt NamKhám Phá Cuộc Phiêu Lưu cùng Suzuki Jimny tại Việt Nam

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Khám phá sự hấp dẫn mạnh mẽ và khả năng vượt địa hình của Suzuki Jimny, hiện đã có mặt tại Việt N...

Nâng cao Trải nghiệm Lái Xe với Xe Suzuki Ertiga Hybrid Nâng cao Trải nghiệm Lái Xe với Xe Suzuki Ertiga Hybrid

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Khám phá sự kết hợp hoàn hảo giữa hiệu suất và phong cách với Xe Suzuki Ertiga Hybrid. Kết hợp cô...

Suzuki Swift: Lựa chọn xe nhỏ gọn và linh hoạt có sẵn tại VNSuzuki Swift: Lựa chọn xe nhỏ gọn và linh hoạt có sẵn tại VN

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Trải nghiệm niềm hứng thú khi lái xe cùng với chiếc xe Suzuki Swift, hiện đã có mặt tại Việt Nam....

Medical Devices Registration in BangladeshMedical Devices Registration in Bangladesh

50 days ago

We help you to prepare Medical Device Technical File (MDR) as per the regulatory requirement of E...

The Routes To Conformity - Navigating EU RegulationThe Routes To Conformity - Navigating EU Regulation

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Conformity Assessment Procedure for Medical Device under the Responsible Model (EU MDR 2017/745 &...

Internal Quality Audit: Key Checks for SuccessInternal Quality Audit: Key Checks for Success

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To achieve and sustain excellence, a company needs a good quality control system. We provide Inte...

Premium Organizational Management ServicesPremium Organizational Management Services

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Take a premium advantage of MAVEN's Premium Organizational Management Services. These services ar...

Annual Maintenance Contract ServicesAnnual Maintenance Contract Services

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We provide best AMC service where we take complete charge of ensuring regulatory compliance of al...

Classification of Medical Devices in VietnamClassification of Medical Devices in Vietnam

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Medical devices in Vietnam are classified by CDSCO, Central Licensing Authority. Medical device o...

What is a Clinical Evaluation Plan and Why is it Important?What is a Clinical Evaluation Plan and Why is it Important?

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A Clinical Evaluation Plan is a document that outlines the systematic process of assessing the sa...

Design History File for Medical DevicesDesign History File for Medical Devices

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Get your Design History File planned and approval for your medical devices in Vietnam, Malaysia, ...

Clinical Development Plan Clinical Development Plan

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A clinical development plan is a subpart of a clinical evaluation plan which aims at the devices ...

EUDAMED - European Database on Medical DevicesEUDAMED - European Database on Medical Devices

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However, the new medical devices regulations (EU MDR) contain important improvements including a ...

MHRA Registration to get UKCA MarkMHRA Registration to get UKCA Mark

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The MHRA Registration database contains manufacturer name, address, MHRA reference (account) numb...

Unraveling the relationship between EN ISO 149711 and GSPR Unraveling the relationship between EN ISO 149711 and GSPR

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The interrelationship between EN ISO 14971:2019/A11:2021 and the General Safety and Performance R...

Overall Residual Risk - How to Evaluate it ?Overall Residual Risk - How to Evaluate it ?

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The risk management standard ISO 14971:2019 is the Holy Bible for medical device risk management....

CE Mark for Medical Devices: Stay AheadCE Mark for Medical Devices: Stay Ahead

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The CE mark is of utmost importance in the European market, and understanding its intricacies is ...

European Medical Device Regulations European Medical Device Regulations

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It has been said that European Medical Device Regulations is the most significant change to the r...

Trusted Biomass Pellets Export Companies in IndiaTrusted Biomass Pellets Export Companies in India

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Seeking trusted Biomass Pellets Export Companies in India? Look no further than 73 Deals! We are ...

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