Regulatory interactions are an essential component of the drug development process, and Pentara plays a critical role in supporting clients through this process. Pentara works with clients to prepare for interactions with regulatory authorities, including the FDA and EMA. This includes preparing briefing documents, writing questions to solicit feedback from regulatory authorities, and providing support during meetings. Pentara also provides guidance on regulatory requirements and helps clients navigate the regulatory landscape. They ensure that clients are in compliance with regulations and guidelines, minimizing potential risks. Regulatory interactions are a vital aspect of drug development, and Pentara provides clients with critical support through this process.