Site Monitoring

We have a very dedicated and experienced team in the monitoring. The clinical monitoring services include:

  • IRB/IEC application preparation, submission and approvals

  • Site specific regulatory binder creation and maintenance

  • Training of site personnel

  • Site initiation visits

  • Clinical site management

  • Interim monitoring/co-monitoring visits

  • Site close out visits

  • CRF retrieval

  • Query management

  • Study materials supply management

  • Vendor supply management



Medclin Research, a pan India Clinical Research service provider to the pharmaceutical industries with over 7 years of experience in clinical studies in various therapeutic areas. We have developed a niche in vaccinology. Our extended service includes publication in index journal, advisor in scientific and marketing activities and participating as a speaker/faculty in various forums to create awareness of the therapy through study results.

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