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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.
On any given drug, APR is able to work through the chemical / physical / technological / pharmacokinetic characteristics of the drug candidate to determine the best option in term of finished dosage form and related development.
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.
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