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The first step of the project Design Planning is the evaluation of the best Regulatory Strategy according to customer requirements. APR is able to plan and manage Scientific Advice Meetings with Health Authorities in either EU and US in order get guidance or validate regulatory and development strategies.
Where the drug candidate/s is/are already defined, APR can exploit the chemical / physical / technological characteristics of the active ingredient/s to determine the valid galenic approach and the best topical form.
This is the last Step of the project Design Planning where APR is able to provide a complete Development Plan including activities, time and costs.