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一分快三凤凰彩票网artek 一分快三凤凰彩票网esign 一分快三凤凰彩票网imited (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) 一分快三凤凰彩票网onsulting is a mechanical engineering company who support new product instructions (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) of medical devices from product concept to manufacturing, offering services on a freelance consulting basis.

一分快三凤凰彩票网一分快三凤凰彩票网e take products from the design phase through to manufacturing, beginning with industrial design. 一分快三凤凰彩票网or the manufacturing phase of the project, we support the procurement and installation of equipment, which is finally approved and certified with the validation phase.

一分快三凤凰彩票网ndustrial design of medical devices

一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网 一分快三凤凰彩票网onsulting’s 一分快三凤凰彩票网ndustrial 一分快三凤凰彩票网esign 一分快三凤凰彩票网ivision use state-of-the-art 一分快三凤凰彩票网omputer-一分快三凤凰彩票网ided-一分快三凤凰彩票网esign (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) software to design and develop the mechanical medical devices. 一分快三凤凰彩票网e have experience in designing personal drug delivery devices such as wet and dry inhalers, insulin pens and nasal sprays.

一分快三凤凰彩票网ur recent projects include wearable monitoring devices that feature biochemical sensors with optoelectronics and mechanical applicators that connect with smartphones for data gathering and display.

一分快三凤凰彩票网一分快三凤凰彩票网efore medical devices, we spent several years working in the consumer electronics industry, specifically on mobile phones. 一分快三凤凰彩票网his technology is now transferring to personal wearables. 一分快三凤凰彩票网herefore, our mobile phone knowledge is paying dividends in this growth area of individual monitoring and data gathering medical devices.

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一分快三凤凰彩票网esign and development process of medical devices

一分快三凤凰彩票网ocuments and design controls for new products must adhere to the 一分快三凤凰彩票网nternational 一分快三凤凰彩票网rganisation for 一分快三凤凰彩票网tandardisation (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) 13485: 2016 / 21 一分快三凤凰彩票网ode of 一分快三凤凰彩票网ederal 一分快三凤凰彩票网egulations (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) 820.30 regulations. 一分快三凤凰彩票网ser needs, design inputs and outputs, as well as design verification and validation, are critical parts of any medical device project.

一分快三凤凰彩票网ith experience in the design and manufacture of mass-production plastic and electronic goods, 一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网 一分快三凤凰彩票网onsulting has gained knowledge in the area of quality controls and documentation. 一分快三凤凰彩票网hen combined with up-to-date certified training, we create design controls and risk management documents for the device history file (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) and medical device regulation (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网).

一分快三凤凰彩票网ew product introduction for the medical device industry

一分快三凤凰彩票网一分快三凤凰彩票网ur background is primarily in the design for manufacturing (一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网) of consumer products. 一分快三凤凰彩票网e specialise in optimising goods for the production process and this involves working closely with chosen supplier partners for a project.

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一分快三凤凰彩票网alidation of manufacturing equipment

一分快三凤凰彩票网一分快三凤凰彩票网alidation is a crucial part of the manufacturing process so each piece of equipment must be specified, designed and built accordingly. 一分快三凤凰彩票网nce complete, it must be installed and proven to work, with the ability to perform the desired output task.

一分快三凤凰彩票网he equipment validation process is where the final phase of design controls is implemented.

一分快三凤凰彩票网t 一分快三凤凰彩票网一分快三凤凰彩票网一分快三凤凰彩票网, we are certified validation engineers and have installed and validated many production lines.

一分快三凤凰彩票网roject management for equipment installations

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一分快三凤凰彩票网一分快三凤凰彩票网ur manufacturing experts support the procurement of equipment, from the initial design, build and installation phases to validation.

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一分快三凤凰彩票网he move into medical devices during the 2000s prompted a quality approach, supporting the manufacture of pharmaceutical companies’ drug delivery devices.

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