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Development of research plans and reports including proposals, timelines, protocols, consent forms, CRFs, SOPs QCR has Phase I-III clinical
operations and medical monitoring experience that can help
your company develop a comprehensive clinical program. We
can offer you a start-to-finish solution by building out timelines,
developing protocols, working closely with Data Management
to design Case Report Forms, and developing working procedures
and Standard Operating Procedures to assure that your trial
is conducted on time, according to GCP/ICH guidelines, and
with quality results. |
