June 2020
Volume 15 Issue 6 |
|
|
|
|
Features
Laboratory automation can reduce the need for in-lab user presence but requires efficient and dependable user—system interface.
/ read more /
Recent drug recalls in the United States from nitrosamine contamination prompt the need for more sensitive impurity testing methods and a re-evaluation of acceptable lower limit levels.
/ read more /
Laboratory automation can reduce the need for in-lab user presence but requires efficient and dependable user—system interface.
/ read more /
|
|
|
Subscribe
Subscribers can enjoy each full issue of Pharmaceutical Technology in print or via the PharmTech app.
subscription offers |
 |
|
|
| |
|
advertisement |
|
In-vitro Skin Models: Development of Topical and Transdermal Formulations
On Demand Presentation
/
View now. / |
| |
|
| |
|
|
News
The quality control from ZeptoMetrix is formulated with purified intact viral particles that have been chemically modified to render them non-infectious and refrigerator stable.
/ read more /
The extension of the company’s product offerings to include the anti-certolizumab pegol antibodies offers critical reagents for the development of assays for TNF alpha inhibitor biologics and their biosimilars.
/ read more /
The company has expanded its microscopy services with the addition of infrared microspectroscopy and hot stage optical microscopy.
/ read more /
|
|
|
| |
New Technology
The kit consists of a test volume of 10 µL, a range of 0.39–25 ng/mL, a lower limit of detection of 0.03 ng/mL, and average inter- and intra-assay coefficients of variation less than 10%.
/ read more /
The company recently launched its OmniTop Sample Tubes adjustable volume sampling system, a single-use system that allows for exact sampling.
/ read more /
|
|
The new filters extend column life and reduce contamination while simplifying sample preparation.
/ read more /
The new chromatography columns provide enhanced separation for high order aggregates and macromolecules.
/ read more /
|
WEBCASTS
Discovery, Formulation, and Performance of Self-Emulsifying Drug Delivery Systems (SEDDS)
Thursday June 4, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Best Practices for Meeting and Exceeding Regulatory Standards in Primary Packaging USP <381> and <382>
Part II: Wednesday, July 22, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST
Comprehensive Analysis into Disintegration Mechanisms: How Reliable Are Textbook Recommendations?
Wednesday, June 10, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST
Your Clinical Results Look Promising, but are you ready for launch? How to build a Robust Packaging Strategy for Rapid Commercialization
Wednesday, June 17, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST
Moderator: Rita Peters, Editorial Director, Pharmaceutical Technology
|
|
|
| |
