Pharsh Pharma Inc. provides analysis and medical writing services for investigator-initiated and industry-sponsored trials. Our services include:

• Protocol Development

We provide sponsors with extensive experience in the development of protocol for every phase in a global working environment. Our extensive therapeutic experience enables us to design protocols for the most complex early Phase I programs, all the way through to the open label observational research programs in the post-approval environment.

• Clinical Study reports for Phases I-IV

We work collaboratively with scientific and medical writers experienced in regulatory requirements to provide clear, concise, and well-constructed clinical study reports.

• Clinical/Statistical Reports