....has shown great flexibility and expertise in regulatory documents and beyond....has continuously demonstrated strong writing and project management skills, and has a great ability to step in quickly and efficiently.CK, Associate Director of Medical Writing, Biogen Idec, USA
Consistently reliable in providing quality documents regardless of the deliverable type requested. Always willing to share expertise and provide improvement opportunities to enhance the document output.Salvatore Curti, Vice President and Head Drug Safety Operations & Mari Welke, Head of Aggregate Reporting, UCB BioSciences Inc.
Justina wrote several clinical study reports for us and we would not hesitate to hire her services again. The work she produced was of high quality, delivered on time and she was easy to work with.Associate Director, Clinical Submissions Writing, UK-Based Biopharm Company