For sponsors and CROs: what makes a US site's clinical trial agreement move faster. Reuse an agreement already negotiated, price standard budget lines in a rate card, settle the legal entity and signer at the start, and run IRB work alongside the contract where the sponsor and IRB allow it.
October 29, 2026·Amavita Editorial (AI-assisted) AI-assisted
Vendor demos follow the vendor's script. How to sandbox-test a CTMS against your own SOPs, source workflow, integrations and finance reports before you sign.
October 26, 2026·Amavita Editorial (AI-assisted) AI-assisted
What 21 CFR 56.108, 56.110, 812.35 and 312.30 require for protocol amendments, where the time goes, and how a Miami cardiovascular site keeps enrollment moving through version changes.
October 26, 2026·Amavita Editorial (AI-assisted) AI-assisted
How to design early feasibility protocols for catheter-based devices with same-day observation: telemetry, serial labs, discharge criteria, safety reporting and imaging.
October 26, 2026·Amavita Editorial (AI-assisted) AI-assisted
Why a dedicated cardiovascular ASC research setting in Miami can start daytime device protocols faster than a tertiary hospital, and when it is the wrong choice.
October 13, 2026·Amavita Editorial (AI-assisted) AI-assisted
Indication map, diagnostics, and same-day Phase 1 work (2 operating rooms and 5 recovery beds in a licensed Kendall cardiovascular ASC) at Amavita Research — without overnight or non-CV claims.
October 13, 2026·Amavita Editorial (AI-assisted) AI-assisted
Amavita Research recruits from an active Miami cardiovascular practice panel instead of waiting on passive referrals. What that changes for screening — and what it does not promise.
Used equipment can build a good site — or quietly disqualify it. Before buying a used ECG or other device for trial work: verify the calibration and service paper trail, confirm the digital export formats central laboratories require, budget IQ/OQ qualification, and run the total cost of ownership.
October 5, 2026·Amavita Editorial (AI-assisted) AI-assisted
Amavita Research is a cardiovascular site. How we plan to add immunology and pursue imaging-enabled oncology and neurology scopes as prime site, and what is not true yet.
October 5, 2026·Amavita Editorial (AI-assisted) AI-assisted
Amavita Research runs cardiovascular Phase 1 work inside an affiliated Kendall, Miami ASC licensed for 2 operating rooms and 5 recovery beds. Same-day outpatient scope.
August 25, 2026·Amavita Editorial (AI-assisted) AI-assisted
Heart failure affects over 6 million adults in the US. Learn about the types, stages, modern treatment options, and how clinical trials are advancing care.
August 22, 2026·Amavita Editorial (AI-assisted) AI-assisted
TAVR has evolved beyond the high-risk population. Here is what referring cardiologists need to know about patient selection, procedural advances, and when to refer in 2026.
How FDA's Diversity Action Plan Final Guidance affects cardiovascular trial site selection: enrollment targets, site demographic profile, sponsor obligations, and how sites like Amavita Research support diverse enrollment in Miami.
When to run a cardiovascular trial across US and Latin America under a single coordinated design: speed-to-FIH, regulatory pathways, patient diversity, cost arbitrage, and operational integration. Amavita Research + bioaccess®.
Comprehensive sponsor decision criteria for evaluating cardiovascular clinical trial sites in 2026: PI continuity, patient flow, contracting speed, cost structure, quality framework, and indication fit.
Plain-language guide for patients considering enrollment in a cardiovascular clinical trial: screening, informed consent, randomization, time commitment, compensation, your rights, and what to expect at every stage.
Plain-language guide to reading a clinical trial informed consent form: what each section means, which sections matter most, common red flags, and questions to ask the trial team before signing.
Plain-language guide for patients with structural heart disease (TAVR candidates, mitral valve, congenital adult patients) considering clinical trial participation. Eligibility, what trials are testing, what to expect.
Plain-language guide for patients who have had a heart attack or unstable angina considering clinical trial participation: what trials are testing, eligibility, what to expect, and current ACS trials at Amavita Research.
Plain-language guide for heart failure patients with iron deficiency considering clinical trial participation: why iron deficiency matters in HF, what IV iron trials are testing, eligibility, what to expect.
Plain-language guide for patients with peripheral artery disease considering clinical trial participation: what trials are testing in 2026, eligibility, what to expect, and current PAD trials at Amavita Research.
Plain-language guide for patients with high blood pressure considering clinical trial participation: what trials are testing in 2026, eligibility, what to expect, and current hypertension trials at Amavita Research in North Miami Beach, FL.
Plain-language guide for patients with heart failure considering clinical trial participation: what trials are testing in 2026, eligibility, what to expect, and current heart failure trials at Amavita Research in North Miami Beach, FL.
On May 13, 2026, Amavita Research performed a coronary stent procedure at the affiliated Kendall ASC (Advanced Cardiovascular of Miami) — a dedicated cardiovascular ambulatory surgery center (ASC) in Miami-Dade. The procedure was led by Dr. Pedro Martinez-Clark.
April 29, 2026·Amavita Editorial (AI-assisted) AI-assisted
Heart failure with preserved ejection fraction (HFpEF) is a type of heart failure where the heart's main pumping chamber squeezes normally but is too stiff to relax and fill with blood properly betwee
April 29, 2026·Amavita Editorial (AI-assisted) AI-assisted
Heart failure with reduced ejection fraction (HFrEF) is a type of heart failure where the heart's main pumping chamber does not squeeze out enough blood with each beat.[1][2][3]
April 29, 2026·Amavita Editorial (AI-assisted) AI-assisted
A pacemaker is a small, battery-powered device implanted under the skin in the chest that helps your heart beat at a normal, steady rhythm by sending mild electrical impulses when needed.
From the first phone call through the final follow-up visit, here is a step-by-step look at what participating in a cardiovascular clinical trial actually involves.
Drug clinical trials are organized into phases. Each one answers different safety and effectiveness questions. Here is what each phase is for, in plain language.
First-in-human (FIH) trials are the first time a new therapy is studied in people. Here is how protocols, oversight, and site experience combine to keep participants safe.
Atherectomy is an endovascular technique that removes or modifies arterial plaque, often used in calcified peripheral artery disease. Here is how it works.
PAD affects millions of adults in the U.S. Learn the warning signs, how it is diagnosed, and the modern range of treatment options — including ongoing clinical research.
TAVR is a minimally invasive procedure that replaces a diseased aortic valve through a catheter — without open-heart surgery. Here is how it works and who it helps.
Eligibility for a cardiovascular clinical trial depends on the study's protocol — but the basic principles are the same across trials. Here is how qualification works.
A clear, plain-language explanation of cardiovascular clinical trials — what they study, how they protect participants, and the role they play in advancing heart and vascular care.