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AF276MO2017536KBL Annex 1: TECHNICAL OFFER Medical Equipment Item No. Item Description Specifications/ Requirements Unit measure Specifications offered by supplier (including Manufacturer Company
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Who needs who technical specification for?

01
Healthcare organizations
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Medical device manufacturers
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Regulatory bodies

What is WHO technical specification for medical devices Form?

The WHO technical specification for medical devices is a document needed to be submitted to the required address to provide some info. It has to be filled-out and signed, which is possible in hard copy, or with the help of a particular solution like PDFfiller. This tool allows to fill out any PDF or Word document directly from your browser (no software requred), customize it depending on your purposes and put a legally-binding e-signature. Right after completion, user can send the WHO technical specification for medical devices to the relevant receiver, or multiple recipients via email or fax. The editable template is printable as well from PDFfiller feature and options presented for printing out adjustment. Both in digital and physical appearance, your form will have got clean and professional appearance. You can also turn it into a template to use later, so you don't need to create a new file from scratch. Just edit the ready template.

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WHO technical specification is a document that provides guidelines and criteria for the development, manufacturing, and validation of health products, ensuring safety, efficacy, and quality.
Manufacturers and suppliers of health products, including pharmaceuticals and medical devices, are required to file WHO technical specification.
To fill out WHO technical specification, one must gather all relevant product information, complete the designated forms accurately, and submit them to the appropriate WHO authority along with any required documentation.
The purpose of WHO technical specification is to provide standardized requirements to ensure that health products meet international safety and effectiveness standards.
The information that must be reported includes product details, manufacturing processes, quality control measures, and compliance with regulatory standards.
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