An European Medicines Agency submission is not an easy task. It is a time-consuming, need experienced people, planning capabilities and strong project management. We offer our support in order reduce time, improve quality of submission and consequently chance of success.
Without a strategy you are not able to identify challanges, allocate resources, define timeline and respect dedlines.
A good Regulatory strategy oversee the whole development process, helping you to save time and money, improving chance of success.
We offer a full range of quality systems and external activities review and audits. Our audits are conducted by experienced professionals who produce audit reports with the highest levels of accuracy and consistency in respect of timelines. We are priced competitively and we are qucik in activation.
We could evaluate your technology or idea and provide you a report with an in dept analysis of:
1) The technical merits and challenges of your invention;
2) The Intellectual Property rights that you may have available
3) The commercial potential and pathways available to commercialise your invention
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