advertisement
 |
|
|
PRODUCTION TRENDS
3D printing is being explored as a manufacturing method for on-demand, personalized medicine.
/ read more /
A multi-purpose biopharmaceutical manufacturing facility using a matrix of multi-functional cleanrooms can be adapted to efficiently meet the capacity challenges of both supplying clinical trials and launching products.
/ read more /
|
|
|
advertisement
 |
Subscribe
Subscribers can enjoy each full issue of Pharm Tech in print, or via Pharm Tech apps.
subscription offers |
 |
|
|
|
|
advertisement
 |
|
|
FROM THE ARCHIVE: EMERGING TECHNOLOGIES
A Q&A with FDA to gain insight on FDA's views of three-dimensional printing and its regulation in drug manufacturing. / read more /
Three-dimensional printing allows unique benefits to be built into solid-dosage forms. / read more /
New approaches enable more patient-centric drug design that offers improved outcomes. / read more /
|
|
|
advertisement
 |
|
|
advertisement
 |
|
|
IN THE NEWS
Leistritz installed a ZSE-3D twin-screw extrusion system at its Somerville, NJ process laboratory that facilitates the development and production of filaments for 3D printing. / read more /
|
|
|
|
|
Editor's Picks
 |
De Lama’s DLVHP/DE pass-box decontamination unit uses vacuum hydrogen peroxide sterilization.
/ read more / |
 |
groninger and SKAN have collaborated to develop Integra, a production line concept that integrates both an isolator and filling machine for vials with a large capacity range.
/ read more / |
|
|
|
UPCOMING WEBCAST
Sterility Testing: Best Practices and Use of Isolator Technology
Tuesday, October 23, 2018 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Register now
Successfully Navigating the Analytical Environment of Complex Generic APIs
Tuesday, October 16, 2018 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Register Now
Facing Inactive Ingredient Database Challenges? Navigating the Complexity for Successful Regulatory Filings
Tuesday, October 2, 2018 at 11am EDT | 10am CDT | 4pm BST | 5pm CEST
Register Now
Moving Beyond the Central Dogma: New Tools and Systems for the Production of Difficult-to-Express Proteins
Wednesday, September 26, 2018 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Register Now
Assessing Product Integrity Risk Profiles and Engineering On-Dose Authentication During Drug Development Process
Thursday, September 20, 2018 at 1pm EDT | 12pm CDT | 10am PDT
Register Now
|
|
EVENTS
Oct. 9–11, 2018 | Madrid, Spain
Oct. 14–17, 2018 | Chicago, IL
more events |
|
|
eBOOK
 |
This eBook covers novel technologies for the formulation, manufacture, purification, and delivery of sterile small- and large-molecule drugs, including single-use systems, facilities and equipment, contamination issues, process analytics, and process modeling.
download the eBook |
|
|
|
|
|
|