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Editorial status
Listed · source-checked
Last reviewed
Jun 24, 2026
Next review due
Jun 24, 2027
Commercial relationship
Listed editorially
Challenge window
Self-reported certifications labeled

PACKAGING LABELING

MRP Solutions

MRP Solutions (Mold-Rite Plastics) is a manufacturer of plastic caps and closures, including child-resistant closures, for the pharmaceutical and nutraceutical industries. Corporate headquarters are in Lake Forest, Illinois, with manufacturing under the Mold-Rite Plastics operation. The company reports ISO 9001 certification, a cGMP environment, and Type III Drug Master File holdings, none of which was independently confirmed against an allowlisted registry.

Lake Forest, Illinois

Directory Listing · Records Reviewed

Public records and independent sources have been reviewed.

What this means →
MOQ
Not publicly disclosed
LEAD TIME
Not publicly disclosed
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§1Editorial assessment

MRP Solutions (Mold-Rite Plastics) is a manufacturer of plastic caps and closures, including child-resistant closures, for the pharmaceutical and nutraceutical industries. Corporate headquarters are in Lake Forest, Illinois, with manufacturing under the Mold-Rite Plastics operation. The company reports ISO 9001 certification, a cGMP environment, and Type III Drug Master File holdings, none of which was independently confirmed against an allowlisted registry.

§2Our review

The six checks in our review, applied before any name appears in the directory. Each check is auto-derived from public evidence on this profile.

Independent confirmation: warn.
Sources we traced: miss.
How recent: pass.
Right to respond: pass.
What they told us: pass.
What we don’t know: pass.

§3Inspection history

§4Certifications

0 of 2 certifications independently confirmed. What this means

§5Capability matrix

PRODUCT TYPES
Caps · Closures · Child-Resistant Closures · Dispensing Closures · Custom Closures
CAPABILITIES
Cap and Closure Manufacturing · Child-Resistant Closures · In-House Tooling · Custom Closure Design · Multiple Facility Network

§6Sources

§7 · What we don't know

  • ISO 9001, cGMP, and the Type III Drug Master File are self-reported and were not independently confirmed
  • MOQ and lead time are not publicly disclosed

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 check-by-check breakdown that produces this vendor's score, see our scoring framework. The connection map between MRP Solutions and other vendors, capabilities, and certifications is in the manufacturer atlas.

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Educational information only. Not legal, regulatory, or professional advice. Inventory Ready provides independent assessments based on publicly available information. See Terms for details.