NanoGuardian and Capsugel in anticounterfeiting alliance
NanoGuardian, a division of US firm NanoInk, has given Capsugel, Pfizer\'s drug delivery division, global access to its NanoEncryption technology that protects capsule-based drugs against counterfeiting.
NanoEncryption technology works directly on capsules, tablets, vial caps, and single-use syringes to provide multi-layered security consisting of overt, covert and forensic security features. It protects drugs against counterfeiting and illegal distribution using a single technology.
The overt and covert security features allow dose-level authentication at any point in the supply chain, while NanoCodes provide comprehensive tracing information on every capsule.
The NanoCodes may be associated with an unlimited amount of manufacturer-determined data, including product information (strength and expiry date), manufacturing information (location, date, batch and lot number) and distribution information (country, distributor, wholesaler and chain). They can also be linked to on-package e-pedigree technologies such as radio frequency identification (RFID) and 2-D barcodes, creating a multilayered protective shield of each individual dose from plant to patient.
"Given the concerning rise in counterfeit and illegally diverted medications throughout the world, we wanted to bring value to our customers by helping to protect their brands, companies, and the patients they serve," said Guido Driesen, president and general manager of Capsugel.
In addition to the traditional NanoGuardian model of using a proprietary machine to implement the NanoEncryption technology, Capsugel will offer pre-NanoEncrypted capsule shells to pharmaceutical companies, eliminating any significant additions to their current manufacturing process.
Capsugel says it expects to supply NanoEncrypted capsules by June 2010.
You may also like
Manufacturing
Lonza expands AAV offering with Xcite AAV stable Producer Cell Line platform to idustrialise Viral Vector Manufacturing
Read moreNew technology demonstrates superior performance versus transient transfection in clinically relevant customer gene of interest and engineered capsid, enabling scalable and cost-effective AAV manufacturing. Launch reflects Lonza’s deep expertise in cell line development, viral vector manufacturing, and platform industrialisation built over decades of supporting complex biologics
Trending Articles
-
You need to be a subscriber to read this article.
Click here to find out more.
You may also like
Manufacturing
Lonza expands AAV offering with Xcite AAV stable Producer Cell Line platform to idustrialise Viral Vector Manufacturing
New technology demonstrates superior performance versus transient transfection in clinically relevant customer gene of interest and engineered capsid, enabling scalable and cost-effective AAV manufacturing. Launch reflects Lonza’s deep expertise in cell line development, viral vector manufacturing, and platform industrialisation built over decades of supporting complex biologics
Manufacturing
Lonza delivers strong performance in Q1 2026 in line with expectations and confirms full-year Outlook 2026
Basel, Switzerland, 8 May 2026 – In its qualitative Q1 2026 business update, Lonza1 reported a strong performance across its CDMO business in line with the expected trajectory for Full-Year 2026. As expected, due to a lower prior year base, campaign timing and product releases, and planned site shutdowns, CER sales growth and CORE EBITDA margin will be notably stronger in the first half of 2026 than in the second half
Manufacturing
Bristol Myers Squibb licenses Lonza ADC linker-payload technology for undisclosed target
BMS has secured exclusive access to Lonza’s SYNtecan linker-payload platform, alongside GlycoConnect and HydraSpace technologies, to advance development of an antibody-drug conjugate against an undisclosed target