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 →- 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
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.
§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
- MRP Solutions Official Website(2026-06-24)
- MRP Solutions Contact / Corporate HQ (Lake Forest, IL)(2026-06-24)
§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.
What We Couldn't Verify
- ISO 9001, cGMP, and Type III DMF status are self-reported; no allowlisted registry was available to confirm them independently
- On-site facility inspection was not conducted
Last reviewed: June 24, 2026
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.
Our Evaluation Method
Every manufacturer assessment follows six principles:
- Evidence: Claims backed by documentation, not marketing copy
- Freshness: Information reviewed and dated within the last 12 months
- Provenance: Sources cited for every key claim
- Challenge: Inconsistencies flagged, not hidden
- Disclosure: Material connections stated directly on affected listings
- Abstention: When we can't assess, we say so explicitly
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