PRECISION. PURITY. CONTROL.
Documented nutraceuticals, peptides, and injectable compounds for clinics and healthcare providers worldwide. Structured to support verification and quality assurance workflows.
Featured Product
Nicotinamide Adenine Dinucleotide—the essential coenzyme for cellular energy and repair. Our NAD+ products deliver uncompromising purity for clinics focused on longevity and regenerative medicine.
Product Catalog
Premium products for healthcare providers and research institutions.
Comprehensive peptide portfolio for research and compounding pharmacies. Bulk supply or complete ready-to-use kits for clinics.
Reduced Glutathione (≥99%) • L-Carnitine Base or L-Carnitine L-Tartrate (≥98%) • Taurine (≥99%) • Methylcobalamin (Vitamin B12) (≥98%) • L-Methionine (≥99%) • 5-MTHF (≥98%) • Sodium Ascorbate (Vitamin C) (≥99%) • Magnesium Chloride (USP injectable-grade) (≥99%) • Zinc Chloride (injectable-grade) (≥98%) • Sodium Selenite (≥99%) • Manganese Chloride (≥99%)
All supplied as lyophilized injectable ingredients in 10 mL vials.
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Minimum order quantity (MOQ) for NAD+: 500 vials
For bulk pricing, email [email protected]
Partner With Us
Expand your brand with premium products under your own label.
We handle manufacturing, testing, and compliance—you focus on growing your business. Our white label program gives you access to premium products with your branding.
Worldwide Operations
One unified standard across every market we serve.
Our strategic presence in North America and Europe enables us to deliver the same uncompromising quality and service standards regardless of location.
Shipping & Logistics
Primary carrier: DHL
Additional regional carriers available based on location
Cold-chain logistics supported when required
Our Standards
Every product meets the highest standards of quality.
From sourcing to delivery, we maintain rigorous quality control processes structured to support verification at every stage. Each batch is tested in accredited U.S. laboratories for identity, purity, potency, and endotoxins. Full Certificate of Analysis (COA) provided with every order.
Independent analytical testing performed by accredited U.S. laboratories
Quality manufacturing standards
Certificate of Analysis (COA) provided with every order
Batch-level documentation from raw material to finished vial
Velara Medical Group maintains controlled documentation practices to support reproducibility, verification, and external review. Records are maintained per batch to support downstream QA and analytical validation.
Velara Medical Group is structured to support independent verification workflows. We routinely provide Certificates of Analysis (COAs), batch documentation, and supporting materials to purchasing clinics and pharmacies and—when designated—directly to accredited laboratories and pharmacy QA teams.
Supporting documentation including Certificates of Analysis, analytical summaries, and batch records are available to purchasing entities and their designated third-party laboratories for quality verification purposes.
Velara Medical Group maintains a clinically neutral position and does not make therapeutic or outcome-based claims. We focus on manufacturing quality, analytical verification, and documentation integrity.
Our internal processes are designed to support repeatable documentation review and external verification by independent laboratories.
Public site content reflects operational structure; formal documentation is provided offline as part of controlled verification workflows.
Independent verification by pharmacy QA teams and third-party laboratories is encouraged.
Technical & Commercial
Technical specifications, regulatory compliance, and partnership details.
Target Market
Our products are formulated exclusively for licensed healthcare providers, compounding pharmacies, wellness clinics, and accredited research institutions. We do not sell directly to consumers.
Quality Assurance
Every batch undergoes rigorous third-party analysis at accredited U.S. laboratories. Testing includes identity confirmation, purity assessment (HPLC), potency verification, and endotoxin screening (LAL). Full Certificate of Analysis accompanies each shipment.
Product Formats
All compounds are supplied as lyophilized (freeze-dried) powder in sterile 10mL glass vials with flip-off caps, designed for reconstitution with bacteriostatic water. We offer Velara-branded packaging or full white-label solutions including custom vial labels, branded boxes, and COA documentation with your company identity.
Applications
Yes. We provide bulk API supply for compounding pharmacies, ready-to-dispense vial kits for clinical settings, and research-grade materials for institutional studies. Our flexible MOQ structure accommodates both pilot programs and large-scale procurement.
Order Requirements
Standard MOQ for NAD+ is 500 vials. White-label programs require a minimum of 500 units per SKU. Volume pricing tiers are available for orders exceeding 1,000 units. Contact our team for custom quotations.
Logistics
Primary carrier is DHL Express with regional alternatives based on destination. Temperature-sensitive shipments utilize validated cold-chain packaging with real-time monitoring. We ship to the United States, Mexico, United Kingdom, and select international markets.
White Label
Standard white-label production requires 30–45 days from artwork approval to shipment. Timeline varies based on packaging complexity, custom inserts, and order volume. Rush processing available for established partners.
Getting Started
Contact [email protected] with your organization details, licensing credentials, and product requirements. Our team will schedule a consultation to discuss specifications, pricing, and fulfillment logistics.
Laboratory Review
Third-party laboratories and pharmacy QA teams commonly evaluate the following documentation:
Contact us to discuss your clinical supply needs. Precision formulations for a healthier future—for your patients.
Contact Our Team