Dispatches from Excipient Fest in Baltimore - UPDATE
As the USP, ICH and US FDA all aim to tackle elemental impurities testing for pharmaceuticals and...
|
Dispatches from Excipient Fest in Baltimore
China’s implementation of GMPs for excipient manufacturers, as well as a developing US FDA-style DMF system, have...
|
Injex says it is looking for partners to prefill its device and Glide will develop Pfenex’s anthrax...
|
International GMP standard facilities and six biopharma centres will lead Russia’s initiative in implementing its Pharma 2020...
|
Project should include participation by supply chain partners
Counterfeiting is a priority across the phamaceutical supply chain. Serialization and Pedigree requirements and solutions are still evolving. I would like to see participation in these types of projects by Manufacturers, Distributors, Retailers and Consumers. Also, the many standards determining bodies, i.e, GS1, HDMA, etc. should be connected to the effort. There needs to be a holistic approach that ties together the many requirements and regulations into one universal solution with defined standards. Many supply chain partners are looking to 2015 and the California mandate. This effort should be synergistic with state and federal regulations.
Posted by Bill Ricigliano
14 October 2010 | 14h31