Introduction
Our Clinical Trial Site
A physician-led clinical trial site dedicated to advancing medical research through excellence, integrity, and patient-centered care. We conduct groundbreaking clinical trials that bridge the gap between scientific discovery and improved patient outcomes.
Our Clinical Trial Services
Phase I-IV Clinical Trials
Patient Recruitment & Retention
Regulatory Compliance Management
Data Collection & Analysis
Site Management & Coordination
Information for Clinical Trial Participants
Your participation in clinical research helps advance medical treatments for future generations
What to Expect
Our experienced team will guide you through every step of the clinical trial process, from initial screening to study completion, ensuring you’re fully informed and comfortable.
Your Safety First
Participant safety is our top priority. All studies are conducted under strict safety protocols with continuous monitoring by our medical team and regulatory oversight.
Informed Participation
We believe in fully informed consent. You’ll receive detailed information about the study, potential benefits and risks, and have all your questions answered before participating.
Participant Rights & Benefits
Your Rights Include:
- The right to withdraw from the study at any time
- Complete information about the study and your role
- Privacy and confidentiality protection
- Access to study results when available
Potential Benefits:
- Access to cutting-edge treatments
- Close monitoring by medical professionals
- Contributing to medical advancement
- Study-related care at no cost
Your Clinical Trial Journey
1. Initial Contact & Pre-Screen
We’ll discuss the study with you and conduct an initial pre-screening to determine if you may be eligible for participation.
2. Consent to Review
After providing consent to review your medical information, we’ll conduct a thorough evaluation of your eligibility for the study.
3. Informed Consent & Screening
You’ll receive detailed information about the study, including potential risks and benefits, followed by comprehensive screening assessments.
4. Baseline Assessments
Comprehensive medical evaluations to establish your baseline health status before beginning the study treatment.
5. Study Participation
Regular visits for treatment administration, monitoring, and assessments according to the study protocol.
6. Follow-up Care
Continued monitoring after treatment completion to assess long-term effects and outcomes.
Our Therapeutic Areas
We conduct clinical trials across diverse medical specialties
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Cardiology
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Neurology
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Endocrinology
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Pulmonology
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Genetic Research
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Preventive Medicine
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General Medicine
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Orthopedics
About Our Clinical Trial Site
Leading clinical research with physician expertise, regulatory excellence, and unwavering commitment to participant safety
Our Mission
As a clinical trial site, we specialize in conducting high-quality clinical research that adheres to the highest standards of scientific rigor, regulatory compliance, and ethical practice. Our physician-led team ensures every study contributes meaningfully to medical advancement.
We partner with leading pharmaceutical companies, biotechnology firms, and research organizations to bring innovative treatments from laboratory to patients, addressing unmet medical needs across diverse therapeutic areas.
“Every clinical trial we conduct is an opportunity to transform lives and advance the future of medicine.”
Why Choose Our Clinical Trial Site?
Physician-led research excellence
Comprehensive participant support
Cutting-edge therapeutic areas
Regulatory compliance expertise
Our Core Values
The principles that guide every clinical trial we conduct
Respect
We treat every participant with dignity, acknowledging their contribution to medical research and prioritizing their comfort, safety, and well-being throughout the trial. Respect also governs our professional relationships with sponsors, regulators, and the wider research community, fostering trust and collaboration.
Integrity
We conduct all activities with unwavering integrity, upheld by three core pillars:
Probity
Uncompromising ethical conduct and honesty in research practices and data reporting.
Transparency
Clear, timely communication with participants, sponsors, and regulatory authorities to ensure accountability.
Discipline
Consistent, rigorous adherence to protocols, ethical standards, and regulatory requirements.
Empowerment
We equip participants with the information and support they need to make informed decisions at every stage of the trial. We also enable sponsors by delivering high-quality data and dependable site performance that accelerate safe, ethical scientific progress.
What Sets Our Site Apart
Three pillars of clinical trial excellence
Physician-Led Expertise
Our clinical trials are overseen by experienced physicians who bring deep medical knowledge and patient care expertise to every study, ensuring the highest standards of clinical practice.
Innovative Research
We conduct cutting-edge clinical trials across multiple therapeutic areas, partnering with leading pharmaceutical and biotechnology companies to advance medical science.
Participant-Centric Focus
Every aspect of our clinical trial operations is designed with the participant in mind, ensuring a comfortable, informative, and supportive research experience from screening to completion.
Our Vision
Our vision is to be the clinical trial site that transforms medical research by putting participants first. We strive to conduct studies where every breakthrough directly translates into safer, more effective treatments for patients worldwide.
We are committed to ensuring that innovation is always driven by the needs and well-being of study participants, contributing to healthier, fuller lives for future patients.
Our Clinical Expertise
Led by experienced physicians and supported by dedicated research professionals, we excel in conducting rigorous clinical trials that meet the highest standards of scientific integrity and participant care.
Our Clinical Trial Methodology
Our approach is built on participant-centered care, emphasizing safety, transparency, and continuous quality improvement:
Collaborative Care
We foster partnerships between participants, investigators, and sponsors, creating a supportive environment that enhances both the research process and participant experience.
Participant Engagement
We begin by listening to participants—understanding their needs, concerns, and expectations—which informs how we design and conduct our clinical trials.
Ethical Trial Conduct
Our clinical trials are meticulously planned and executed to prioritize participant safety and data integrity, ensuring every protocol meets the highest ethical and regulatory standards.
Rigorous Quality Oversight
Continuous monitoring and quality assurance ensure each trial maintains the highest standards, with clear communication channels maintained throughout the study duration.
What Our Participants Say
Real experiences from clinical trial participants
Join Us in Advancing Medical Research
Whether you are a sponsor seeking a reliable clinical trial partner, an investigator looking to collaborate, or a participant interested in contributing to medical advancement, Ameli-Biogroup LTD is here to ensure excellence at every step.
One trial at a time. One breakthrough at a time.
Contact Our Clinical Trial Site
Ready to partner with us or participate in groundbreaking research?
For Participants
Interested in participating in a clinical trial? Learn about our current studies and how you can contribute to advancing medical research.
Learn About StudiesFor Sponsors
Partner with our experienced clinical trial site for your next study. Let’s discuss how we can support your research objectives with excellence.
Partner With Us“At Ameli-Biogroup LTD, every clinical trial we conduct and every decision we make is driven by our unwavering dedication to advancing medicine through ethical, high-quality research.”
Contact us today to learn more about our clinical trial capabilities and current research opportunities.