Our expert knowledge of the regulatory framework and environment are your leading advantages to ensuring a successful clinical study. As your local partner, Sponsor goals can be achieved and barriers overcome.

Lucerent is able to assist with the following regulatory services:

• Support the local PI(s) in submitting regulatory documentation and ongoing annual continuing review reports
  

• Represent the PI and/or Sponsor at meetings requested by the National Ethics Committee
  

• Coordinate with local companies to ensure proper approval, storage and distribution of products