Regulatory submission package

At Aepodia, we provide services to help you design and implement your biopharmaceutical (CTD 2.7.1) and clinical pharmacology (CTD 2.7.2) plans, to support your compound registration.

We draw on our project management and phase I units network to manage parallel trials and implement your plan observing optimal and competitive timelines.

Our study coordinators and skilled staff ensure data is of a high quality and effectively registered.