Neva’s management team has over 125 years of collective pharmaceutical industry experience to support its clients. This includes time in your shoes, solving challenges ranging from technical & scientific to timelines & budgets. From this background, Neva’s guidance for product, process, method development/validation and beyond, is not only expert but also uniquely reasoned and imaginative. Our team has worked in the global biotech/pharma industry on a range of products in both the R&D (non-GMP) and the QC (GMP) laboratory settings, as well as for the process development and manufacturing of research, clinical and commercial medicinal products. Plus, our team has extensive experience with global regulatory agencies in order to share insights regarding compliance and regulatory aspects of QC/analytical and processing activities.