
PTSM: Pharmaceutical Technology Sourcing and Management
- PTSM: Pharmaceutical Technology Sourcing and Management-12-06-2017
- Volume 12
- Issue 12
Recipharm Equips Three More Facilities for US Serialization
The facilities in Brescia, Italy and Karlskoga and Uppsala, Sweden, are the latest of Recipharm’s sites to be equipped to supply serialized products to the United States.
	Contract development and manufacturing organization (CDMO), Recipharm, 
The facilities in Brescia, Italy and Karlskoga and Uppsala, Sweden, are the latest of Recipharm’s sites to be equipped to supply serialized products to the US. The CDMO now has nine facilities in total that are ready to offer serialization capabilities.
Following a EUR 40 million investment into its company-wide implementation program in 2016, Recipharm has already delivered more than 1.3 million serialized and aggregated packs to markets such as China, South Korea, Saudi Arabia, and Turkey where serialization regulations are currently in place.
	“In addition to equipping nine of our sites ahead of the EU deadline and the new US enforcement date, we’ve also introduced a serialization task force to ensure a consistent roll out of our standard solution across all of our facilities,” Staffan Widengren, director of Corporate Projects at Recipharm and head of the global steering committee for Recipharm’s serialization project said in a 
“The investment we’ve made in terms of time, money, and resource means we’re well prepared ahead of time and a lot of our customers are already on-boarded. We can now refocus our attention on ensuring we realize the additional benefits of serialization implementation including improving line efficiencies and streamlining logistics operations,” Widengren said in the same release.
The next facilities to be equipped will be the company’s facility in Bengaluru, India, which will supply serialized products for the US.
	Source: 
Articles in this issue
almost 8 years ago
Improving Taste to Enhance Medication Adherencealmost 8 years ago
Taking a Holistic Approach for Data Governancealmost 8 years ago
Does Your Endotoxin Detection Method Ensure Patient Safety?almost 8 years ago
Lonza in Gene Therapy Licensing Agreementsalmost 8 years ago
Will Pharma Meet the Drug Tracking Deadline?almost 8 years ago
Best Weighing Practices in the Pharmaceutical Industryalmost 8 years ago
Avista Doubles API Manufacturing Capacity at Colorado Facilityalmost 8 years ago
Cambrex Expands Small-Scale Capacity at Iowa Facilityalmost 8 years ago
Nitto Avecia Completes Large-Scale Synthesis of OligonucleotideNewsletter
Get the essential updates shaping the future of pharma manufacturing and compliance—subscribe today to Pharmaceutical Technology and never miss a breakthrough.





