Pharsh Pharma provides sponsors with extensive experience in the development of protocols for every phase in a clinical trial.

 

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
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We give first thought to the needs of patients in Sub-Sahara Africa and committed to efforts to train and improve the capacity of all stakeholders to properly conduct clinical trials.

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