Led by experts in FDA and ISO regulations, this team ensures all Pure Rx products meet or exceed U.S. and international quality standards. They monitor every stage of production — from raw material sourcing to final batch release.
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- cGMP and ISO 9001:2015 oversight
- WHO GMP alignment and facility audits
- Labeling compliance (FDA, FTC, Prop 65, AB 1341, etc.)
- Rigorous third-party batch testing with COAs for each product

Staffed by healthcare professionals and medical science liaisons, this team provides hands-on support to clinics, medspas, and providers. They assist with dosing, patient education, reconstitution, and clinical best practices.
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- Provider onboarding and clinical training
- Dosing and titration guidance (GLP-1, GLP-2, etc.)
- White-glove support for advanced therapies and combo blends
- Education on compliance, consent, and liability

All our client accounts are assigned a personal Pure Rx Representative who will assist you throughout your journey with us.
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Our business development and partnerships team helps grow Pure Rx’s national footprint as well as yours by creating high-value collaborations with physicians, med spas, clinics, wellness centers, and distributors.
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- National and regional account acquisition
- Affiliate, white-label, and co-branding programs
- Strategic alliances with labs, telehealth groups, and pharmacies
- Educational events, conference representation, and speaking engagements

Our SCI team ensures product availability and quick turnaround by maintaining an agile, U.S.-based supply chain. With strategically stocked inventory and domestic sourcing, we eliminate the delays and shortages common in traditional compounding.
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- Credible and tested raw material procurement
- Inventory forecasting and logistics
- Batch tracking and cold-chain optional fulfillment
- Custom white-label and private-label distribution support

Our compounding specialists and pharmacists oversee production across our ownership and national network of Laboratories as well as 503A and 503B licensed pharmacies. They ensure precision, sterility, and purity with every vial, ampoule, or blend — supported by cleanroom-level fill-finish and advanced lyophilization methods.
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- Sterile and non-sterile compounding
- Peptide blending and unit dose configuration
- Fill-finish execution under aseptic conditions
- Endotoxin-free and USP-grade material handling

Our R&D scientists focus on formulating cutting-edge peptides and biologics with enhanced stability, absorption, and efficacy. Our team rapidly prototypes and scales novel formulations to meet evolving clinical demands.
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- Custom peptide design & innovation
- Formulation and delivery optimization
- Lyophilization research and proprietary freeze-dry tech
- Pipeline expansion based on emerging literature and provider feedback