
Clinical Trial Supply
- QS-21 used in 5 globally approved vaccines
- 200–400M human doses annual supply capacity
- End-to-end cold chain & customs compliance

FDA-Registered Wholesaler
GMP Certified
EXCiPACT Certified
VuRoyal Pharmaceutical's FDA Approved Drugs and Resources category provides research organizations, clinical trial sponsors, and vaccine developers with compliant access to Reference Listed Drugs, vaccine adjuvants, and clinical trial supply. Products meet USP, FDA, and GMP standards, supported by end-to-end supply chain and regulatory guidance services.

You can verify FDA drug approval status using the FDA's online Drugs@FDA database, which lists approved drug products including Reference Listed Drugs (RLDs) and Reference Standards (RS). VuRoyal also provides access to FDA Orange Book and Purple Book reference drugs and can assist qualified organizations in identifying and sourcing verified, FDA-compliant reference listed drugs for clinical and research use.
Talk to our experts for custom solutions and tailored guidance.

Supplies FDA Orange/Purple Book reference drugs and analytical standards for clinical trial sponsors and CROs.

Provides QS-21 and other adjuvants for human and veterinary vaccine R&D across infectious disease programs.

Delivers reference standards and listed drugs essential for bioequivalence testing and generic drug submissions.

Sources specialty and hard-to-find medicines with cold chain logistics for hospitals, clinics, and pharmacies.
Talk to our experts for custom solutions and tailored guidance.
As the exclusive partner of Desert King International in China, VuRoyal provides sole-source access to QS-21 and other leading vaccine adjuvants used in globally approved vaccines.
From international procurement and customs clearance to cold chain transportation, VuRoyal manages the full supply chain with FDA, USP, and DSCSA regulatory compliance at every step.
Backed by decades of pharmaceutical R&D experience, VuRoyal offers complimentary regulatory consultation for imported drug approval registration, reference preparation selection, and clinical trial filing.
Submit your inquiry and our pharmaceutical experts will respond with sourcing options, compliance guidance, and tailored supply chain solutions.
For immediate assistance, feel free to give us a direct call at +1 617-870-2690 You can also send us a quick email at
For immediate assistance, feel free to give us a direct call at +1 617-870-2690 You can also send us a quick email at