Medical Monitoring Services
Medical monitoring services across a wide range of studies and therapeutic modalities.
Our medical monitoring team are experienced pharmaceutical physicians with clinical experience and deep therapeutic knowledge in a range of modalities including orphan drugs, oncology agents and cell and gene therapies.
We provide medical monitoring and oversight, and support at all phases of clinical trials to protect the safety and well-being of all clinical trial participants.
Operating in line with GCP requirements, our experienced medical monitors spend time at the outset of a clinical study to gain a deep understanding in order to provide strategic oversight to optimize protocols for recruitment rates, patient satisfaction and retention. Our medical monitors work with you to provide the required support for the duration of the study through to study close out.
We know that having an experienced, and subject-knowledgeable medical monitor can be pivotal to timely study success. The Medical Monitors at Boyds possess this unique combination of clinical and research experience to add significant value to both the investigative and sponsor teams.
Our experienced medical monitors work with sponsors, the sites and project teams to carry out the following:
- Subject eligibility review
- AE/SAE review including case history clarification, answering queries arising from Investigators, facilitating CIOMS Narrative Review and sign-off
- Work alongside the study team, attending meetings as required
- Pharmacovigilance activities
- Study completion activities: Contributing to the writing of the clinical study report, review of all tables, listings and figures, culminating in sign off of the clinical study report as medical monitor