What we do

The Elpida Sciences team supports all aspects of the clinical trial process, from feasibility and planning to managing the trial through to completion.

Feasibility Assessments

We provide accurate feasibility assessments to target and study timelines to ensure we are fully compliant with the requirements of a clinical trial. Our investigators have the knowledge and expertise to deliver clinical trials safely and in accordance with your study timelines.

Our experience covers (but is not limited to) the following areas:

  • Musculoskeletal

  • Dermatology

  • Cardiovascular Disease

  • Diabetes

  • Respiratory

  • Women’s Health

  • Vaccines

  • Medical Devices

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Prescription Medication

Study Award / Start up Clinical Trials

At Elpida Sciences, we fully understand the importance of an efficient and speedy study start-up. That’s why we appoint our clients with a single point of contact to ensure an effective and consistent approach, which leads to shorter timelines in terms of budget and contract management.   

In parallel, we enter into contract negotiation with local vendors (if their services are required as part of a clinical trial) and patient identification and engagement so that everything is in place to achieve that all-important first patient enrolled in a study protocol.

 

Patient Recruitment

We have developed effective strategies for patient identification, engagement, recruitment and retention so we can be confident of successfully delivering your trial. We pride ourselves on our ability and commitment not only to achieve or exceed our target recruitment but to retain our clinical trial volunteers.

Our investigators have experience in recruiting the first patient in clinical trials both globally and nationally and ensure patient compliance with a clinical trial to deliver studies to your target and timelines.

Blood Pressure Check
 
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Quality Assurance and Compliance

Our comprehensive Standard Operation Procedures cover all processes to ensure we are fully compliant with the stringent regulatory, ethical and ICH/GCP standards that govern clinical trials.

Our research team also carries out both external and internal audits, making sure our data is of high quality whilst meeting data entry compliance rules and timelines, in accordance with the study contract.