There are many advantages to choosing Qualipak for your contract packaging needs. We have an experienced staff to manage your jobs from start to finish. We work with your schedule to offer you the rapid turn around time you need for your products. We have the extra capacity you need during peak seasons. Our wide range of equipment and large production facility eliminate the need for you to purchase costly equipment. We are your Contract Packing Division, without the overhead!

Qualipak's Quality Assurance/Quality Control program is second to none. Our full-time QC staff and Production Supervisors receive annual training in all facets of our quality process. We perform annual internal quality audits. Every employee receives annual GMP training. We also train each employee on every job they perform. And we can customize our quality process to meet your needs. All of our customers do things a little differently so our program is flexible enough to handle all your quality requirements.

Our employees also receive extensive safety training. Our training includes, but is not limited to, all OSHA mandated safety training. We train in areas such as MSDS, Fire Extinguisher/Prevention, Ergonomics, First-Aid and CPR, Bloodborne Pathogens, Lockout/Tag-out, Emergency Action Plans, and much more.

Qualipak uses a "Job Track" software program, written specifically for us, to track all materials from the time they arrive in our warehouse until they leave our buildings as finished goods, leftovers or rejects. Job Track, not only tracks product by item number, control number, and job number, it also tracks products by location. We assign pallet numbers to each pallet that we receive and track its movement through the production process in our Pallet Location System. Job Track also allows us to customize our reporting process to give you the information you need, when you need it. We generate custom receiving, production,and shipping reports for many of our customers.

We are also in the process of validation our computer system per FDA Regulation 21CFR Part 11(ERES), Electronic Records/Electronic Signatures. This validation will also include 21CFR Part 820 (QSR's), Quality System Regulation and 21CFR Part 211(GMP), Good Manufacturing Practice for Finished Pharmaceuticals. We plan on completing the validation by April 15, 2002

Whatever your contract packaging need, we have the staff, experience, flexibility and dedication to customer service to exceed your expectations!