Newsletter | August 28, 2018

08.28.18 -- Scientists Discover First Step Toward Finding A New, Targeted Lung Cancer Treatment

 
Industry Insights
Simplify Cell Detachment Processes With Serum-Free Media
Poster | By Anna-Barbara Hachmann, Andrew M. Campbell, and Stephen F. Gorfien, Thermo Fisher Scientific

Vaccine production with adherent cell lines faces multiple challenges that include selection of a suitable vessel, detachment of cells for scale up, optimization of infection, as well as harvesting of virus particles. In this study we identified ways to simplify the process and evaluated stirring techniques to measure the viable cell densities for the production of the rabies virus surrogate, vesicular stomatitis virus, in Vero cells.

Stripping Membranes For Reprobing
Article | GE Healthcare Life Sciences

Detect more than one protein by chemiluminescence on the same Western blot membrane by stripping and reprobing the membrane with a different primary antibody.

Opportunities In Preclinical Development
White Paper | IDBS

Find ways to optimize holistic preclinical development.

Fighting The Opioid Epidemic: How Gr√ľnenthal's Abuse-Deterrent Technology Contributes
Case Study | Patheon

While the wider use of opioids has led to many benefits for patients in pain, it also has led to higher incidences of misuse, abuse, and development of opioid addiction. 

Pharmaceutical Manufacturing Industry Challenges
Infographic | Dassault Systèmes BIOVIA

The FDA expects organizations to have full visibility and control over their processes — with shared responsibility for contract manufacturing.

Solvents, Polymers, And Cyclones: Bioavailability Enhancement Through Spray-Dried Dispersions
Webinar | Catalent

Very few new molecular entities in active clinical development are readily bioavailable, and when dosed at escalated levels, even these may not be sufficiently absorbed. Learn how spray-dried amorphous dispersion might help.

Most Popular News
Solutions
ZipDose Technology
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Bio-Rad Laboratories, Inc.
Online Training

Elemental Impurities Tests For Pharmaceutical Products According To The New ICH Q3D And USP 232/233 Guidelines
Date: Tuesday, August 28, 2018 • Time: 1:00 pm EDT

Laboratory Data Integrity: Current Expectations For OOS Result Investigations
Date: Wednesday, August 29, 2018 • Time: 1:00 pm EDT

Developing A Part 11 Compliance Plan In Clinical Research
Date: Tuesday, September 11, 2018 • Time: 1:00 pm EDT

Key Elements Of Pharmaceutical Serialization And Track And Trace Systems: Implementation And Compliance Best Practices
Date: Wednesday, September 12, 2018 • Time: 1:00 pm EDT

Preparing eCTD Submissions: A Step-By-Step Guide
Date: Tuesday, September 18, 2018 • Time: 1:00 pm EDT

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