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The first step of the project Design Planning is the valuation of the best Regulatory Strategy according to costumer requirements. An accurate classification study according to the 93/42/EEC Directive (or equivalent 510K in the US) and related amendments is necessary. If needed, APR is able to manage a Scientific Advice meetings with the Notifying Body or Health Authority in either EU and US.
Where the main component/s is/are defined, APR can make the most of its/their chemical/physical characteristics to determine the most suitable galenic approach and to develop the best form for the intended topical device.
This is the last Step of the project Design Planning: APR is able to provide a complete Development Plan including activities, time and costs.