We help manage interactions with Patient Advocacy Groups (PAGs) to improve patient engagement. We can also manage the creation of patient registries and patient information networks (PINs) and related patient engagement efforts.
Using PINs and other online tools, and working with IRBs, we create and collect patient journey maps, natural history data, and clinical data necessary for client submissions to FDA and EMA.
Working with patients and patient advocacy groups should begin as early as possible in the life of a biopharma or medical device startup. And those relationships don't stop at approval, but continue throughout the product life-cycle. We can help plan and budget for this process.
We can help ensure your data collection efforts comply with applicable US and European laws and regulations.