Regulatory Consultant

WHO Prequalification of In-Vitro diagnostics

In Vitro diagnostics, who, Med Device Quality Consulting, Regulatory Consultant,

WHO PQ – What, How and WHY ? World Health Organisation Prequalification (WHO PQ) programme helps countries having low and […]

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COMPLIANCE WITH ELECTRONIC IFUs

EU MDR, Electronic IFU, Regulatory Consultant, Regulatory Affairs Consultancy, Regulatory Affairs Agency,

Practical Guide Well, in our previous blog on electronic IFUs, we discussed that e-IFU requirements are not mandatory to comply

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Asean mdd

Medical Device Regulatory Affairs, Regulatory Consultant, Medical Device Regulatory Consulting,

The Association of South East Asian Nations (ASEAN) is a regional bloc composed of ten countries: Brunei Darussalam, Burma, Cambodia,

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Applying Usability Engineering to Medical Devices

Medical Devices, Regulatory Consultant, Medical Device Regulatory Consultants in India,

Usability engineering for medical devices, or human factors engineering, is a concept of understanding interactions between the user and the

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