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Körber Pharma Packaging
Körber is an international technology group with around 10,000 employees and more than 100 locations worldwide.
We turn entrepreneurial thinking into customer success and shape the technological change. In the Business Areas Digital, Pharma, Supply Chain, Tissue and Tobacco, we offer products, solutions and services that inspire.
At the Körber Business Area Pharma we are delivering the difference along the pharma value chain with our unique portfolio of integrated solutions.
Swiss-based Körber Pharma Packaging is a specialist developer and producer of highly integrated, modular and automated solutions and systems for pharmaceutical secondary packaging. Dividella Solutions describe a highly distinctive modular and integrated approach to secondary packaging for the pharmaceutical industry based on specific expertise in integrated and monomaterial solutions and of the packaging requirements for parenteral products and forms a key part of the integrated offer by pharmaceutical and biotech experts Körber Group and its Business Area Pharma.
Product and service offerings
Patented Dividella NeoTOP top-loading and NeoTRAY feeding systems form the basis for solutions that have continually evolved to provide the most up-to-date, patient-friendly and environmentally responsible solutions and form the basis for complete secondary packaging solutions for medicinal parenteral products that can be difficult to stack, such as needles, injector pens, vials and syringes.
Körber Pharma Packaging top-loading and side-loading solutions, along with patented feeding systems, enable product handling with extreme care and safety while maintaining high output.
Körber Pharma Packaging implements a customer-orientated service, focusing on identifying the optimal packaging solution for any client, with the ideal solution chosen according to production volume, batch size and packaging requirements. All top-loading styles of packaging can be produced on Körber Pharma Packaging flexible and adaptable NeoTOP packaging systems, whether for clinical trials or establishing a market presence or full product launches; when packaging high volumes of low count packs the NeoTRAY concept is the best fit.
The packaging systems are designed with high attention to detail and precision, with each machine optimised for various load sizes. The NeoTOP x handles small to medium-sized lots, whereas the NeoTOP 804 and 1604 are designed for medium to large-sized lots and the NeoTRAY for high output and large lots.
Customers also benefit from Körber Pharma Packaging’s extensive engineering support, working in partnership with clients to identify and develop optimized solutions for the safe packaging of sensitive products. Körber Pharma Packaging’s process is guided by the supreme goal of minimizing total cost of ownership (TCO) and total cost of package (TCP) through the use of monomaterials, optimized pack sizes for cold chain and simplicity for the end user.
The modularity of Körber Pharma Packaging’s solutions extends past machine design to packaging formats and integration with other offerings from Körber Business Area Pharma, delivering enhanced functionality, flexibility and reduced overall costs. An almost unlimited number of packaging formats can be accommodated, with high emphasis on monomaterial solutions that deliver powerful bottom line and sustainability benefits.
Over more than 40 years, Körber Pharma Packaging has established a proven record of accomplishment in highly innovative and effective solutions for secure and flexible handling and packaging of pharmaceutical products. Based in Grabs in the Canton of St. Gallen in eastern Switzerland, the company counts 20 of the world’s largest pharmaceutical companies among its clients, including the top ten.
Quality, Regulatory and Standards
Körber is a leading source of expertise and solutions in highly regulated industries with intimate knowledge of the regulatory requirements that govern data security and integration as well as medical devices and GxP operations, such as ISO 9001, EU GMP Annex 11, FDA 21 CFR Part 210/211, and Part 11 — Electronic Records / Electronic Signatures (ERES), as well as In Medical Device Regulation (MDR) and Regulation (EU) 2017/745 on medical devices, ISO 13485, FDA 21 CFR Part 820 and Part 11.
The company’s quality management is licensed to DIN EN ISO 9001:2015 standards. It offers business management and validation services that follow GAMP® 5 guidelines on best practices, such as risk-based, scalable V-model or alternative procedures. Its services also comply with current regulations for client industries, e.g. EU GMP Annex 11; FDA 21 CFR Part 210/211, and Part 11; or ISO 13485.