We understand the nuances of successfully running a global, cardiovascular outcomes trial (CVOT). That’s why we have staff in medical leadership, project management, clinical operations, pharmacovigilance and statistics with CVOT experience who can execute trials using proven effective strategies.
As your cardiovascular CRO, we deliver rapid study start up timelines, on time deliverables, proactive risk management and quality data, achieving study timelines within projected budgets. We understand that small biotech companies need a partner who can complement their limited staff and be sensitive to budget restrictions.
We are experienced in working with smaller biotech companies in a variety of models and can easily adapt to your needs. Our individual cardiovascular group provides a small CRO feel with all the benefits of being a large CRO.
Our Cardiovascular Clinical Experience
We have extensive experience in cardiovascular clinical trials and research, including new therapies such as stem cells, HFpEF, HFrEF, SGLT-2 inhibitors and large, global CVOTs. Our experts have created strategy plans that expedite timelines and deliver superb data quality while adhering tightly to sponsors’ budgets. We have worked on indications for cardiovascular drugs in the following areas:
- Acute coronary syndrome
- Angina pectoris
- Cardiothoracic surgery
- Deep vein thrombosis
- Heart failure
- Ischemic heart disease
- Peripheral arterial disease
- Pulmonary hypertension
- Renal failure (acute and chronic)
- Venous thromboembolism (VTE)
Capturing High-Quality Cardiovascular Clinical Data Safely, With Global Consistency
Our web-based electronic endpoint adjudication system is specially tailored for long-term, large-scale, global cardiovascular clinical trials and research. We use it together with our innovative data monitoring strategies, which employ risk-based techniques encouraged by regulatory authorities to improve patient safety while providing cost efficiencies.