Neozene teams have worked at all levels of project development and with myriad challenges and development concerns. Let our knowledge and experience work for you to more efficiently develop your protocol or development program, with the following clinical trial support services:

  • Budgets and Contracts
  • Grants and Investigator Payments Management
  • Regulatory
  • Protocol Development
  • CRF Development

Whether your new product is a drug, a biologic, a device or a combination, our experience is ready to work with you to set and deliver on aggressive timelines that control costs. The Neozene support services expertise benefits your project during all phases of development, whether it is preparing the IND or IDE to facilitate the first studies in humans or preparing an application (Marketing Authorization Application (MAA), New Drug Application (NDA), Pre-Market Approval (PMA) or 510k) for review by regulatory authorities.