We offer regulatory affairs services for our manufacturing clients to help minimize product development time and accelerate product approval. Our expert team can provide guidance and potential solutions to regulatory hurdles and is experienced in handling a wide range of therapeutic areas and project types, from pharmaceutical to supplements and cosmetics, sterile to non-sterile and repackaging to manufacturing licenses.

Our team provides customized regulatory affairs services based on need and stage of development and works with the client’s internal or 3rd-party regulatory teams to review submissions to ensure compliance with local regulatory requirements.