Inserts, Outserts, & More – Rely On Gooding For Pharmaceutical MicroFolders
At Gooding, we concentrate on integrating progressive concepts and state-of-the-art equipment into the production of inserts, outserts, and more. We strictly adhere to current good manufacturing practices and standard operating procedures, as well as all statistical process controls. We also follow the lean manufacturing philosophy of maximizing value and minimizing waste. Simply put, you can rely on our team for the finest results and service.
"Our approach to doing business has evolved to include forging a partnership with each of our customers. This means collaborating with clients to meet the ever-increasing challenges posed by new FDA regulations and also carefully researching their operations to determine the best way to serve them. This consultative philosophy helps our clients become more cost-effective and attain measurable results.”
Our focus on efficiency and quality eliminates the burden of managing your printing requirements. When it comes to the pharmaceutical industry, our service options prove invaluable. There are countless matters to consider when packaging prescriptions drugs and substances. Fortunately, we can create all the booklets, guides, and inserts required to distribute your product.
Technology & Controls
We have invested in specialized technology and equipment for printing MicroFolders, including the following tools and materials. Our materials will help you align with all FDA regulations.
Vijuk folders allowing for up to 266-panel RTAs
Bar code creation, scan, and verification
Short run digital printing for medical device informational pamphlets and DFU (Directions For Use)
A part 21 CFR compliant optical comparator that scans all press sheets and provides a pixel-to-pixel match of master approved documents
A Perfecta cutting system providing added productivity and accuracy through the binding process
Rigorous Control Processes
Thanks to our rigid and thorough quality control standards, which are a proven combination of strict guidelines and checks and balances, you will access high-quality products – on time and on budget. Gooding has consistently passed the most critical audits because of these controls.
Following CGMP, we adhere to stringent standards at every step of every project. All materials are rigorously segregated and quarantined. We also incorporate total documentation control into the production process, which is why we say: “If you didn’t document it, you didn’t do it.” No order goes out the door without meticulous traceability.