Advancing Healthcare Through Clinical Research
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.
Trusted by Sponsors
Reliable data, audit-ready documentation, sponsor-aligned operations
State-of-the-Art Facility
Dedicated research rooms, secure storage, on-site lab processing
Diverse & Dedicated Team
Board-certified PI and experienced research coordinators on every study
Proven Enrollment Focus
Established cardiometabolic population with structured screening workflows
A High-Performance Clinical Research Site for Cardiometabolic & Device Trials
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.
- Board-certified physician oversight on all research protocols
- Experienced research coordinators and dedicated study staff
- Diabetic, hypertensive & cardiometabolic patient access
- Medical device validation expertise
- High data quality standards and SOP-driven operations
- Fully ICH-GCP, FDA & HIPAA compliant
Operational Standards
- Informed consent-first participant workflows
- Strict protocol adherence & deviation documentation
- HIPAA-aligned privacy and data handling
- IRB oversight — central & local experience
- Audit-ready source documentation at all times
- Physician on-site for all study procedures
- Retention-focused visit coordination
- Budget transparency with sponsors
Meet Our Research Leadership
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. She serves patients throughout the San Fernando Valley, Los Angeles, and Orange County.
Therapeutic & Study Focus
Our investigational experience spans cardiometabolic, regenerative, and medical device categories — supported by an established patient population and dedicated research infrastructure.
Site Capabilities
HealthWatchers360 operates a dedicated research laboratory with appropriate infrastructure to support clinical trials across multiple phases, from single-site to multi-center studies.
Regulatory Standards & Compliance Framework
Every study at HealthWatchers360 is conducted within a rigorous compliance framework aligned with international and federal regulatory standards.
What Sponsors Rely On
- Consistent, protocol-compliant data collection
- Timely enrollment relative to site commitments
- Regulatory binder accuracy and completeness
- Transparent communication on enrollment and deviations
- Experienced coordinators familiar with GCP requirements
- Efficient site activation timeline
- Patient retention through structured follow-up
"We operate with a sponsor-focused mindset while maintaining a patient-centered approach."
Why Partner With HealthWatchers360?
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.
Therapeutic Expertise
Deep clinical experience in diabetes, hypertension, cardiovascular health, metabolic disorders, and medical device validation. Experience in prospective, randomized, and cross-over study designs.
Recruitment & Retention Strength
Established patient population of diabetic, hypertensive, and cardiometabolic patients. Strategies include EMR pre-screening, physician referral network, community outreach, and retention-focused visit coordination.
Protocol-Driven Operations
Efficient site activation timelines, consistent enrollment performance, high protocol adherence, and experienced coordinators who adapt quickly to sponsor EDC and reporting systems.
Full Site Infrastructure
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.
Submit a Feasibility Inquiry
We welcome feasibility discussions, site qualification inquiries, and protocol reviews from sponsors and CROs.
Participate in Clinical Trials. Advance Medicine.
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.
How Clinical Trials Work
How Clinical Trials Work
- Pre-screening — a brief form and review to see whether a study may be a match.
- Initial assessment — meet our team, review the study details, and ask questions.
- Study participation — visits and procedures follow a structured, IRB-reviewed protocol.
- Compensation & follow-up — compensation and follow-up are provided when applicable (study-dependent).
Frequently Asked Questions
Are clinical trials safe?
All studies follow defined protocols and safety procedures. Participation includes informed consent and ongoing oversight appropriate to the study.
Will I be compensated?
Some studies provide compensation for time and travel. Eligibility and compensation vary by study.
Can I leave a study once I've started?
Yes. Participation is voluntary and you may withdraw at any time without impact on your regular medical care.
Do I need health insurance to join?
Not always. Requirements vary by study. Our coordinator will clarify details during screening.
Participation is not a substitute for medical care. All personal information is handled confidentially per HIPAA. I agree to be contacted regarding research opportunities at HealthWatchers360.
What to Expect
- Our team will review your information and contact you shortly
- A study coordinator will discuss current studies with you
- Complete an initial eligibility screening
- If eligible, enroll and participate with full informed consent
- Right to withdraw at any time — no impact on your regular care
Refer Your Patients to HealthWatchers360 for Clinical Trials
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.
- Enhance patient options with access to cutting-edge treatments
- Contribute to advancing medical science and patient care
- Maintain physician oversight — we keep you updated on your patient's progress
- Collaborate with a high-performance, IRB-approved research site
- Dr. Maryam Seddigh (PI) will follow up with you directly
"Together, we can advance medical knowledge and improve patient care through ethical, well-conducted clinical trials."
All patient information is kept confidential and handled in accordance with HIPAA regulations. I confirm I have permission to share patient contact information (if applicable).
Therapeutic Areas for Referral
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.
Ready to Connect With Our Research Team?
Whether you are a sponsor, CRO, physician, or prospective participant — our research leadership welcomes your inquiry.