HealthWatchers360 is a dedicated outpatient clinical research center delivering high-quality data, efficient enrollment, and regulatory excellence. We conduct physician-led investigations in cardiometabolic, cardiovascular, regenerative, and medical device research — fully ICH-GCP, FDA & HIPAA compliant.
Participation in investigational studies is voluntary. Investigational treatments or devices may not provide direct medical benefit.
Reliable data, audit-ready documentation, sponsor-aligned operations
Dedicated research rooms, secure storage, on-site lab processing
Board-certified PI and experienced research coordinators on every study
Established cardiometabolic population with structured screening workflows
HealthWatchers360 is a dedicated clinical research center committed to delivering reliable data, efficient enrollment, and regulatory excellence. We partner with pharmaceutical companies, medical device manufacturers, and CROs to execute clinical trials with precision and integrity.
Founder & Principal Investigator
Dr. Maryam Seddigh is a respected physician with over 15 years of experience in regenerative and integrative medicine. As an integrative physician, she combines evidence-based Western medicine with complementary approaches to address the root causes of disease rather than merely treating symptoms. She provides a full range of non-surgical and minimally invasive procedures with a strong emphasis on safety, precision, and natural outcomes.
As Principal Investigator, Dr. Seddigh oversees regulatory compliance, protocol adherence, and data integrity across all research studies at HealthWatchers360. She serves patients throughout the San Fernando Valley, Los Angeles, and Orange County.
Our investigational experience spans cardiometabolic, regenerative, and medical device categories — supported by an established patient population and dedicated research infrastructure.
HealthWatchers360 operates a dedicated research laboratory with appropriate infrastructure to support clinical trials across multiple phases, from single-site to multi-center studies.
Dedicated spaces for protocol procedures and assessments
Dedicated workspace for sponsor/CRO clinical research associates
Controlled access with documented chain of custody
Validated cold storage with continuous monitoring systems
In-house sample processing with local lab coordination
Experience with major EDC platforms; trained for sponsor systems
Standard Operating Procedures for all study activities; documentation maintained for immediate inspection readiness at all times
Every study at HealthWatchers360 is conducted within a rigorous compliance framework aligned with international and federal regulatory standards.
At HealthWatchers360, we understand sponsor priorities. Our site is built around the operational and data quality standards that sponsors and CROs depend on for successful trials.
Deep clinical experience in diabetes, hypertension, cardiovascular health, metabolic disorders, and medical device validation. Experience in prospective, randomized, and cross-over study designs.
Established patient population of diabetic, hypertensive, and cardiometabolic patients. Strategies include EMR pre-screening, physician referral network, community outreach, and retention-focused visit coordination.
Efficient site activation timelines, consistent enrollment performance, high protocol adherence, and experienced coordinators who adapt quickly to sponsor EDC and reporting systems.
Private research exam rooms, CRA monitoring room, secure investigational product storage with temperature monitoring, on-site lab processing, and audit-ready documentation at all times.
We welcome feasibility discussions, site qualification inquiries, and protocol reviews from sponsors and CROs.
Your participation may help advance medical research while giving you access to innovative treatments and compensation for your time. Your safety and privacy come first — always.
All studies follow defined protocols and safety procedures. Participation includes informed consent and ongoing oversight appropriate to the study.
Some studies provide compensation for time and travel. Eligibility and compensation vary by study.
Yes. Participation is voluntary and you may withdraw at any time without impact on your regular medical care.
Not always. Requirements vary by study. Our coordinator will clarify details during screening.
Partner with a trusted research site to provide your patients access to cutting-edge treatments and contribute to medical advancement. We respect your primary relationship with the patient throughout the process.
Throughout the clinical trial experience, we respect your primary relationship with the patient. Our goal is to foster a collaborative relationship that serves your patient's best interest — not to replace you as the patient's healthcare provider.
Whether you are a sponsor, CRO, physician, or prospective participant — our research leadership welcomes your inquiry.