The ultimate goal of a clinical development programme is to aim for the successful registration of the product (whether a medicine, medical device or other related product). Whether the registration of the product is for the US market (via FDA), EU (via EMA) or other national regulatory bodies across the world, ACROSS Global can assist you with your specific product registration requirements.
We provide consultation services using experts to provide you with the appropriate documentation requirements, pathway (including clinical trials if applicable), timelines, and costs (including regulatory fees) to register your product. We have expertise across medicines (e.g., innovative products, bioequivalents, biosimilars, biologics, orphan products) vaccines, and medical devices / in-vitro diagnostics.
We see Product Registration as the pinnacle of your clinical development programme, and the gateway to your return on investment. Our experts are available to take you across the finishing line to successful registration and beyond.