Vici Health Sciences
Vici Health Sciences operates a pharmaceutical R&D center of excellence in Elkridge, Maryland, providing end-to-end drug and supplement development services. The company holds cGMP, GLP, and DEA (Schedules I-V) certifications. Vici's team has developed over 50 formulations, participated in more than 30 clinical trials, and secured FDA approvals for over 15 ANDAs. For the nutraceutical sector, Vici offers formulation development, analytical method validation, stability testing, cGMP clinical supplies manufacturing, and FDA regulatory consulting. Their pharmaceutical-grade approach to supplement R&D provides a higher bar of analytical rigor than typical contract manufacturers. Vici also joined the Contract Laboratory Network, making their capabilities discoverable to brands seeking independent testing and development partners.
Elkridge, Maryland
Directory Listing · Records Reviewed
Public records and independent sources have been reviewed.
What this means →- MOQMOQ (Minimum Order Quantity)The smallest production run a manufacturer will accept for an order.
- Not publicly disclosed
- LEAD TIMELead TimeThe time from order placement to finished product delivery.
- Not publicly disclosed
§1Editorial assessment
Vici Health Sciences operates a pharmaceutical R&D center of excellence in Elkridge, Maryland, providing end-to-end drug and supplement development services. The company holds cGMP, GLP, and DEA (Schedules I-V) certifications. Vici's team has developed over 50 formulations, participated in more than 30 clinical trials, and secured FDA approvals for over 15 ANDAs. For the nutraceutical sector, Vici offers formulation development, analytical method validation, stability testing, cGMP clinical supplies manufacturing, and FDA regulatory consulting. Their pharmaceutical-grade approach to supplement R&D provides a higher bar of analytical rigor than typical contract manufacturers. Vici also joined the Contract Laboratory Network, making their capabilities discoverable to brands seeking independent testing and development partners.
§2Six-gate readout
Six gates we apply before any name appears in the directory. Each gate is auto-derived from public evidence on this profile.
§3Inspection history
§4Certifications
0 of 3 certifications independently confirmed. What this means
§5Capability matrix
- PRODUCT TYPES
- Formulation Development · Analytical Method Validation · Stability Testing · Clinical Supplies Manufacturing
- CAPABILITIES
- Pharmaceutical-Grade Formulation R&D · Nutraceutical Product Development · Analytical Method Validation · Stability Testing (ICH Guidelines) · Clinical Trial Supplies · FDA Regulatory Services · CMC R&D Consulting
§6Sources
- Vici Health Sciences - Official Website(2026-03-26)
- Vici Health Sciences - Nutraceutical Manufacturing(2026-03-26)
- Contract Laboratory Network - Vici Profile(2026-03-26)
Dietary supplement manufacturers must comply with 21 CFR Part 111 (Current Good Manufacturing Practice for dietary supplements). This includes requirements for personnel, facilities, equipment, production, laboratory operations, and record-keeping.
Disclosures
- No material connection exists between Inventory Ready and this company
For the gate-by-gate readout that produces this vendor's score, see our six-gate scoring readout. The connection map between Vici Health Sciences and other vendors, capabilities, and certifications is in the manufacturer atlas.
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