From the strategic planning of product development programs (beginning with early pre-clinical research, analytical method development and manufacturing) through to the design and implementation of the vital human intervention studies and the eventual health claims submission, P2F Ventures can help clients to understand the requirements of the European Food Safety Authority (EFSA) process and to design and implement a successful high quality development program.

Finding the right clinical research facility is critical and we can help to identify and qualify potential facilities through our in depth experience of running GCP trials.

Whether your ultimate goal is full commercialisation of a consumer product or a business-to-business licensing deal P2F Ventures can support you to achieve that goal.

Understanding the reasons behind the success of failure of previous health claim applications and the factors limiting commercial success can be critical to achieving success in the future.