Relive Health Memorial Houston

Our Quality Promise

Quality is at the core of everything we do. It’s reflected in our team, our client experience, and the results we deliver. If your treatment doesn’t meet expectations, we’ll work closely with you to make it right because your satisfaction and trust matter most.

Your Safety, Our Top Priority

Client safety is our top priority at every step. That’s why every Relive Health Memorial Houston client begins their journey with comprehensive bloodwork and a physical exam with our provider. We continue to monitor progress regularly and offer direct access to our Client Advocate and provider through a private line, so support is always just a call or text away.

How We Vet Our Pharmacy Partners

Client safety is our top priority at every step. That’s why every Relive Health Memorial Houston client begins their journey with comprehensive bloodwork and a physical exam with our provider. We continue to monitor progress regularly and offer direct access to our Client Advocate and provider through a private line, so support is always just a call or text away.

Relive Health partners almost exclusively with 503A compounding pharmacies rather than 503B outsourcing facilities. This means each prescription is prepared based on a specific client and provider relationship. Pharmacies must show valid licensure in the state or states they ship to, and FDA and state board of pharmacy inspection records are reviewed as part of our vetting process.

Some of our partnered pharmacies hold PCAB accreditation (Pharmacy Compounding Accreditation Board), which signifies high standards in sterile and non-sterile compounding, documented quality control processes, staff training, and operational SOPs. While not always required, PCAB accreditation is highly preferred.

For injectables such as semaglutide, tirzepatide, B12, and testosterone, the pharmacy must provide documentation of sterility testing, endotoxin testing, and potency validation, along with Certificates of Analysis (COAs) from FDA-registered API sources. Compliance with USP standards (USP <797>, <795>, or <800> depending on formulation type) is required.

We verify where the active pharmaceutical ingredients (APIs) are sourced from, whether they come from FDA-registered manufacturers, and for GLP-1s, whether the peptides are recombinant and sequence-verified rather than synthetic knockoffs.

Our pharmacy partners must offer formulations aligned with Relive’s protocols. Dosing must allow for precision titration and align with Relive’s in-house algorithms.

We vet for no history of disciplinary action, a clean track record with state boards and the FDA, and HIPAA compliance in all communication and data transfer.

We require our pharmacy partners to have systems in place for tracking and reporting adverse events, as well as lot traceability for quick recall or investigation if needed.

Our Standard For Product Quality

  • Medication Quality (Compounded Drugs)

    All compounds are made in USP-compliant facilities with precision formulations, validated dosing, and stability data. Active pharmaceutical ingredients are sourced from FDA-registered manufacturers, and every batch includes a Certificate of Analysis confirming identity, purity, potency, and microbial safety. Sterile injectables are tested for sterility and endotoxins, then stored and shipped in validated packaging with compliant labeling.

  • Clinical Services Quality

    Our providers are trained in functional medicine, hormone optimization, and metabolic health, with ongoing education and peer-reviewed guideline adherence. Every care plan is built on biomarker-driven decisions and regular lab monitoring, with dosing adjusted based on your individual clinical response and progress over time.

  • Supplement Line Quality (Revive MD)

    All Revive MD supplements are manufactured in cGMP-certified facilities and third-party tested for heavy metals, microbial contamination, and potency. Labels are fully disclosed with no proprietary blends, and Certificates of Analysis are available for every batch confirming label accuracy, ingredient safety, and microbiological standards.

Success Stories at our Houston Center

Your Questions About Quality and Safety

Most peptides used in wellness settings are not FDA-approved drugs for general wellness use. The FDA has approved some peptides for specific purposes, but many others are studied and used in functional and integrative medicine for their potential to support recovery, metabolism, and healthy aging. At Relive Health Memorial Houston, our approach with peptides is not about treating or curing disease. We use them as tools to help support cellular function, energy, recovery, and longevity in clients seeking proactive wellness optimization.

Most of what we offer in functional medicine and wellness does not fall under FDA approval. The FDA approves drugs and medical devices, but wellness approaches including nutrition, supplements, advanced labs, and lifestyle protocols are regulated differently. Our approach is evidence-informed, meaning we draw from both peer-reviewed research and clinical experience to guide our recommendations, even when certain tools or supplements are not FDA-approved medications. We are transparent that supplements and many advanced lab tests are not FDA-approved to diagnose, treat, cure, or prevent disease. We use them as tools to personalize wellness plans, and you are always empowered to decide what feels right for you.

FDA approval means a drug or device has gone through the FDA’s formal review process for a specific indication. Evidence-informed care means our protocols are guided by peer-reviewed research and clinical experience, even when a specific tool or supplement has not completed that formal approval process. Functional medicine is a complementary approach that works alongside conventional care. Our protocols emphasize lifestyle, nutrition, and natural support, which often have not gone through the FDA’s pharmaceutical approval process but have other forms of clinical and traditional evidence behind them.

Every compounded medication we prescribe comes from pharmacy partners that have been vetted for 503A compliance, sterility and potency testing, API source verification, and legal standing with state boards and the FDA. Sterile injectables are tested for sterility, endotoxins, and particulates before they reach our clients. Certificates of Analysis are required for every batch, and our providers monitor your response through regular and follow-up consultations throughout your treatment.

No. Compounded medications are prepared specifically for an individual client based on a provider’s prescription. They are not mass-produced generics. At Relive Health Memorial Houston, we work exclusively with 503A compounding pharmacies, meaning every prescription is tailored to your specific needs, dosing requirements, and clinical profile. This allows for a level of personalization that off-the-shelf medications cannot provide.

Address

9311 Katy Fwy E,
 
Houston, TX 77024

Hours

Mon: 9am – 3pm

Tue: 9am – 5pm

Wed: 12pm – 7pm

Thu: 9am – 5pm

Fri: 9am – 5pm

Sat: 10am – 3pm

Sun: Closed