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DRUG SAFETY MEDICAL MONITORING

DRUG SAFETY MEDICAL MONITORING

by admin

Patient safety is the greatest priority when conducting clinical trials. At Wizard, the Medical Affairs team operates with the highest levels of accuracy, responsiveness and ethics — earning the respect of investigators and clients alike. Wizard’s safety physicians monitor and participate in all phases of clinical trials of interactions with investigators and the site staff regarding the protocol, inclusion and exclusion criteria for patients, safety and lab assessment and medical questions, laboratory and radiology imaging data, cardiac imaging and patients safety issues that take place during the clinical trials.
Our extensively trained medical staff (MDs, RNs, and PAs) and Pharmacists work closely with clients, internal teams and investigator sites to ensure strict adherence to all protocols, as well as GCP/ICH guidelines. Our medical safety officers are available to the investigators and investigators sites and the study team, 24 hours a day globally

  1. Our core services include
  2. Medical monitoring
  3. Protocol waiver and compliance assessment
  4. Serious adverse events (SAEs) surveillance (24-hour coverage)
  1. Lab safety review
  2. Medical data review
  3. Endpoint adjudication