The client is an India-based generic company and was looking for Regulatory support for multiple SPL conversions and submissions to the USFDA. The project presented several challenges, such as stringent timelines, multiple validation errors, and new guidelines for SPL conversions. Freyr’s team had to showcase its technical expertise in content, artwork, packaging, and design activities. By offering 24x7 support to meet the timelines, Freyr was able to accomplish the task of making successful submissions in two (02) weeks’ time.
Learn how Freyr was able to make timely SPL submissions to the USFDA with cost benefits of over 50%. Download the proven case.