For Patients
Learn how to safely participate in a BioPartners study and help advance diagnostic and therapeutic innovation.
Your Health. Your Experience.
Your Contribution to Medical Progress.
At BioPartners, we conduct safe, ethical, and professionally managed clinical studies that help advance new diagnostics, treatments, and medical knowledge.
By choosing to participate, you play an essential role in improving healthcare for future generations — while receiving support from our friendly and highly trained clinical team.
Our California research site offers a comfortable, private, and welcoming environment for all volunteers.
Every study we conduct follows strict guidelines to protect your safety, privacy, and well-being.
Why Participate in
a Clinical Study?
People participate in clinical research for many reasons:
- Access to new diagnostic tests and medical evaluations
- Personalized attention from trained clinical professionals
- The opportunity to contribute to scientific and medical progress
- Compensation may be provided for time and travel (depending on the study)
- Helping improve healthcare for others
Participation is always voluntary, and you may withdraw at any time without penalty.
What You Can Expect?
Our goal is to ensure that you feel informed, respected, and supported throughout the entire study process.
Here’s what typically happens when you join a study:
Learn About the Study
- The purpose of the study
- What will happen during your visits
- How long participation lasts
- Possible risks and benefits
You will receive an Informed Consent Form (ICF) to review and discuss with our team.
Study Visits
- Answering health questionnaires
- Providing a sample (swab, blood, urine, saliva)
- Using a diagnostic device
- Completing surveys
Our clinical staff will guide you at every step to ensure your comfort and understanding.
Eligibility
Screening
All information you provide is handled confidentially and securely.
Dedicated Support
Throughout the Study
- Friendly, GCP-trained Clinical Research Coordinators
- A Principal Investigator overseeing your medical safety
- A private, professional clinic environment
- Clear instructions before, during, and after each visit
Your comfort and care always come first.
Your Safety Comes First
BioPartners follows strict guidelines and regulations to ensure your rights and safety are always protected:
- All studies are reviewed and approved by an Independent Review Board (IRB)
- Staff are trained according to Good Clinical Practice (GCP)
- Your information is protected under HIPAA privacy laws
- You may ask questions at any time
- You may stop participating whenever you choose
Your safety, dignity, and privacy are central to everything we do.
Who can participate?
We conduct studies involving:
- Healthy volunteers
- Adults with specific medical conditions
- Pregnant or postpartum individuals (for specific diagnostic studies)
- Participants of all ages, backgrounds, and communities
Each study has different eligibility requirements — our team will guide you through them.
Current & Upcoming Studies
Active & Upcoming Clinical Studies at BioPartners
BioPartners is currently enrolling volunteers for several clinical research studies at our California research site.
Our studies help develop new diagnostic tests, medical devices, and healthcare tools that can improve patient care for future generations.
Participation is voluntary, and compensation may be provided for your time and travel.
Your safety, privacy, and comfort are always our top priorities.
Diagnostic Swab Collection Study
Study Type:
Diagnostic Performance / Swab Collection
Eligibility:
Adults 18+ (with or without symptoms)
Visit Duration:
10–20 minutes
Compensation:
Yes
Overview:
Participants will provide a self-collected or clinician-collected swab to help evaluate a new diagnostic test for infectious diseases.
The procedure is quick, non-invasive, and performed by trained staff.
Blood Collection for Biomarker Research
Study Type:
Biospecimen Collection (Blood)
Eligibility:
Adults 18+
Visit Duration:
15–30 minutes
Compensation:
Yes
Overview:
Participants will donate a small blood sample to support the development of new laboratory tests and disease biomarkers.
All collection procedures follow strict safety protocols.
Device Usability & Self-Collection Study
Study Type:
Usability / Human Factors
Eligibility:
Adults 18+, able to perform simple at-home or on-site device tasks
Visit Duration:
20–40 minutes
Compensation:
Yes
Overview:
Volunteers will test a user-friendly medical device or self-collection kit.
Feedback helps researchers improve device safety and ease of use.
Respiratory Health Study
Planned Start:
Coming soon
Eligibility:
Adults with cold/flu-like symptoms
Type:
Swab collection + questionnaire
Compensation:
Yes
Women’s Health Diagnostic Study
Planned Start:
Diagnostic Performance / Swab Collection
Eligibility:
Pregnant or postpartum women (study-specific criteria apply)
Type:
Non-invasive swab collection
Compensation:
Yes
How to Participate
Joining a study with BioPartners is simple, safe, and fully guided by our research team.
Step 1. Apply
Our team will review your information and identify studies you may qualify for.
Step 2. Pre-Screening
- Your medical history (if relevant)
- Study requirements
- What to expect during your visit
- Any questions you may have
This conversation is private and secure.
Step 3. Enroll & Participate
Our team will guide you throughout the appointment to ensure a safe and comfortable experience.
Step 4. Follow-Up
- Ensure your well-being
- Gather additional information (if required)
- Provide study updates
You may reach out to us anytime with questions.
Privacy & Participant Rights
Your Privacy and Safety Are Our Top Priorities
BioPartners follows strict ethical, legal, and regulatory standards to protect your personal data and identity.
We safeguard your information through:
- Secure data encryption
- Coded participant IDs (your name is never attached to research samples)
- Restricted-access systems for clinical staff only
- HIPAA compliance
- IRB-approved procedures
All identifiable information is removed before analysis to ensure complete confidentiality.
You have the right to:
- Receive clear and complete study information
- Ask questions at any time
- Decide whether to participate
- Withdraw at any time without consequences
- Have your data protected with the highest privacy standards
Your trust and safety mean everything to us.
FAQ
We are always here to support you. If you have questions about how studies work, eligibility, compensation, safety, or privacy, please visit our FAQ section or contact our research team.
What is a clinical study?
A clinical study helps researchers understand how new diagnostic tests, medical devices, or procedures work in real-life settings.
These studies provide important information that can improve healthcare and advance scientific knowledge.
Why should I consider participating?
People join clinical studies for different reasons, including:
- Access to new diagnostic tests
- Personalized attention from trained clinical staff
- Contributing to medical research
- Helping improve healthcare for future patients
- Compensation for time and travel (depending on the study)
Participation is always voluntary.
Is it safe to participate in a study?
Yes. Your safety is our top priority.
Safety protections include:
- Review by an Independent Review Board (IRB)
- Trained clinical staff following Good Clinical Practice (GCP)
- Oversight by a licensed Principal Investigator
- Monitoring for any side effects or concerns
- The right to stop participating at any time
Every study is designed to minimize risk.
What types of studies do you conduct?
BioPartners conducts:
- Diagnostic test studies
- Biospecimen collection studies
- Device usability and self-collection studies
- Observational studies
- Research involving questionnaires or interviews
Most of our studies are non-invasive or minimally invasive.
Will I be paid for participating?
Many studies offer compensation for your time, effort, and travel.
The amount varies by study and will be explained during the screening or consent process.
What happens during a study visit?
A study visit may include:
- Answering health questions
- Providing a sample (swab, blood, urine, saliva)
- Using a diagnostic device
- Completing surveys or questionnaires
Your clinical coordinator will explain everything before each step.
How long does a study visit take?
Visits may last anywhere from 10 minutes to 1 hour, depending on the study type.
Your coordinator will let you know the expected duration in advance.
Will my personal information remain private?
Absolutely. BioPartners follows strict privacy standards.
We protect your information by:
- Assigning coded participant IDs
- Storing your name separately from research data
- Using secure, encrypted systems
- Limiting access to authorized clinical staff
- Complying with HIPAA, IRB requirements, and data protection regulations
Your identity is never shared with sponsors or outside parties.
Can I stop participating once the study begins?
Yes.
You may withdraw at any time, for any reason, without losing access to future care or benefits.
Your decision will never affect your relationship with our team.
What is an Informed Consent Form (ICF)?
The ICF is a document that:
- Explains the study purpose
- Describes what will happen during participation
- Lists possible risks and benefits
- Outlines your rights as a participant
You will have time to read it, ask questions, and decide whether to join — no pressure, no obligation.
Who reviews and approves the study?
Every study is reviewed and approved by an Independent Review Board (IRB).
The IRB ensures:
- Ethical conduct
- Protection of participant rights
- Clear and accurate consent forms
- Safety of all participants
The IRB continues oversight throughout the entire study.
Who will see my data or samples?
Only authorized BioPartners clinical staff can access your identifiable information.
Any data or samples shared with researchers or sponsors are de-identified — meaning they cannot be traced back to you.
Your privacy is always protected.
Do I need health insurance to participate?
No.
Health insurance is not required, and your insurance will not be billed for study-related procedures.
How do I know if I’m eligible for a study?
Eligibility depends on factors such as:
- Age
- Health conditions or symptoms
- Pregnancy/postpartum status (for some studies)
- Medical history
- Study-specific requirements
Our screening team will help determine whether a study is a good fit for you.
How do I apply to participate?
Joining a study is easy:
- Submit a short online application
- Complete a brief pre-screening call
- Attend a study visit if eligible
- Receive follow-up communication (if needed)
Who can I contact with questions?
Our team is always here to help.
If you have questions about eligibility, safety, or the study process, please contact our research staff at any time.