Limited-time offer: 
About PLP
Trusted supply-chain partners for brands ready to grow.
We help clients focus on marketing, customer acquisition, and expansion while PLP handles peptide supply-chain needs: sourcing, compounding, testing support, labeling, packaging, and fulfillment planning.
Built around controlled protocols and repeatable production.
The PLP quality story is centered on controlled production, documented work, sterile handling, batch review, and repeatable manufacturing lines designed for wholesale volume.
cGMP protocol workflow
Controlled procedures, documented batch records, material traceability, line clearance, and quality review.
ISO Class 5 work-area language
Critical open-vial operations are organized around controlled-area discipline and aseptic handling practices.
Semi-automated lines
Repeatability, throughput, and fill consistency are supported while operator oversight remains in the loop.
Southern California production means more control and faster fulfillment.
PLP is located in Southern California, giving the team direct control over production, scheduling, quality review, and packing without overseas drop-shipping or customs handoffs.
API sourcing
FDA-approved API suppliers are reviewed for each requested compound before production moves forward.
Compounding
PLP compounds products directly and controls formulas, production schedules, batch records, and quality checkpoints.
Vial preparation
Incoming vials move through inspection, washing, high-purity rinse, filtered drying, visual checks, and documented staging.
Filling & packing
In-house filling, freezing, batch handling, and wholesale packing keep orders moving without overseas customs delays.