In Phase I / Bioequivalence

PharmaNet offers a comprehensive range of clinical development and consulting services for early stage programs, including Phase I and bioequivalence studies. PharmaNet conducts early stage programs for international sponsors through our global network of resources.

Scientific/Medical Writing

Scientific and medical writing teams work in collaboration with our scientists, regulatory affairs, and quality assurance personnel to produce:

 

Protocols and informed consent forms
Certified translations of ICF and study materials (French and English)
IRB submissions
Interim, safety, and final reports
Clinical, integrated clinical, and statistical reports
Electronic reports
Scientific abstracts and publications
PharmaNet Development Group, Inc.504 Carnegie Center, Princeton, NJ 08540Tel 609 951 6800Fax 609 514 0390