Ergomed Clinical Monitoring

Ergomed plc

Ergomed Clinical Monitoring

Effective clinical monitoring is essential to a successful trial and expediting a drug’s successful launch onto the market

Clinical Surveillance Pharmaceuticals, Biotechnology & Drug Discovery Technologies

Do you know anyone using Ergomed Clinical Monitoring?

Setting up the first site in a trial is a major milestone but the last site is just as important, maximizing the potential for patient recruitment. Our highly trained, expert and safety-oriented clinical research professionals provide clinical trial monitoring services that are tailor-made to your protocol.

Working together with site management and study physician support, the clinical monitoring team embodies Ergomed’s patient-centric approach to help you navigate all stages of a clinical trial. Our clinical trial monitoring team has a minimum of an undergraduate degree in life science or equivalent education and experience, and an average of four years of clinical research experience, with experience across all phases of trials.


  • Site identification and selection, performing on-site or remote pre-study visits

  • On-site or remote site initiation, interim and close-out monitoring visit activities

  • Verification that the rights and wellbeing of clinical study’s participants are protected

  • Monitoring to confirm consent, eligibility, safety and data integrity

  • Training of investigational site staff

  • Informed consent/document translation, verification and back-translation

  • Preparation of regulatory or ethics/review board submissions

  • Timely submission of protocol/consent and other documents

  • The storage of drugs, management of intellectual property and clinical study materials

  • Reporting of protocol deviations

  • Regular reporting

Ergomed Clinical Monitoring

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