When developing a regulatory strategy, our focus is entirely on co-creating the most effective pathway to approval, institutional review boards and ethics committee processes. Our team of experts are involved at an early stage, reverse journey mapping a strategic pathway from the desired outcomes and charting backwards to the first steps we need to take together. Almost like time travellers, our team ensures the right strategy is in place from the beginning, with a focus on aligning regulatory milestones with clinical trial objectives. With over xx dossier and ODD submissions, xx IND/IDE submissions and xx+ Device Approvals both locally and globally, together we can accelerate human health and wellness.