Industry-leading Quality
Systems. From start
to finish.

quality process

You deserve the highest-quality contract manufacturing and packaging services every single time. This is why our industry-leading Quality System extends throughout the supply chain—from product receipt to final delivery—at every Multi-Pack Solutions™ facility. This ensures quality products and timely delivery you can count on. Complete traceability comes standard here, along with full EPA and FDA compliance. You also have access to our innovative in-house labs for verification and testing solutions. We have a proven track record of creating smart, go-to-market solutions—all supported by a robust Quality System.

Superior Quality Systems and procedures for continuous improvement.

The Multi-Pack Solutions Quality Program extends throughout our organization. This exacting series of comprehensive audits includes numerous customer and regulatory audits each year to help support continuous improvement to our procedures, systems and processes. From receipt to shipment, we control your materials and are focused on quality:

  • Corrective and preventive action processes
  • Fully traceable product materials
  • Incoming raw material and component inspections and testing
  • In-process checks and finished product inspections
  • State-of-the-art USP Purified Water System—tested daily at point of use
  • Accelerated and long-term stability testing
  • Package integrity studies
  • Customized testing and inspection schedules
  • Laboratory testing
  • Supplier Audit Program

We also adhere to a daily S.Q.D.I.P. System to drive excellence: Safety, Quality, Delivery, Inventory, Performance.

Chemistry Labs

Multi-Pack Solutions offers a one-stop shop for complete control. From our new validated walk-in Stability Chamber to our HPLC’s and GC’s and TOC Analyzer, we provide the in-house lab capabilities you need for accurate testing, validation and custom manufacturing, with fast results. And our wet chemistry capabilities (USP/NF & FCC) are unsurpassed in the industry. If we don’t have the proper equipment for your testing, in many cases we can procure it.

  • Stability Testing—Accelerated and Room Temperature
  • Compatibility testing—container vs. contents
  • Validations (Equipment Cleaning, mixing, filling/packaging, test method)
  • Method Transfer validations
  • Analytical and Wet chemistry testing

Microbiology Lab

With a microbiology lab on-site, what usually takes five days takes two days instead. This allows you to identify challenges earlier during testing and adjust accordingly. (We understand speed-to-market is imperative for our customers.) Plus, you are in complete control of the process. Multi-Pack Solutions can also make our own media for growth promotional testing and use vendor-supplied media as well. We can perform quality sampling for our compressed air system and surface & air sampling and testing. And we can identify microorganisms using gram staining, selective media, biochemical tests and our Biolog identification system for critical identifications.

  • USP—Total aerobic count
  • Total yeast and mold count
  • USP—E. coli screening
  • P.aeruginosa screening
  • Salmonella spp. screening
  • S.aureus screening
  • C.albicans screening
  • Biolumix rapid methods system
    (Micro result in two days)
  • Total aerobic count
  • Microbial limits preparatory tests; validation
  • Antimicrobial effectiveness testing
    (Preservative effectiveness)

ISO Certification for Medical Devices

Multi-Pack Solutions is ISO 13485:2016 certified at our Greenville facility, which addresses the Medical Device directives, regulations and responsibilities, as well as demonstrates a commitment to safety and quality of the devices. We have also created a mature Quality Control and Quality Assurance department to ensure our products meet quality standards required by the FDA, ISO 13485:2016, and our customers. Because of this commitment to quality, our customers know they’re receiving quality products every time.


Our Greenville, South Carolina, facility is registered with the FDA and fully FDA compliant to FDA 21 CFR Part 11, 210, 211 for Drugs and 820 for Medical Devices. Our facility has an excellent history with the FDA and we’re very proud to share the details of past FDA Inspections with our customers and potential customers. Reliable FDA mixing, packaging and testing capabilities are not easy to find and we have the experience and Quality Programs you can trust to get the job done right every time.


Our Greenville, South Carolina, facility is registered with the EPA and compliant with application regulations.