SGS Life Science Services | Recorded the 09-Oct-2013 | Webinar
2013 is a landmark year for biosimilars, with the approval of the first biosimilar mAb and regulatory developments across the globe. Correctly interpreting...
Exploring New Frontiers in Direct to Patient (DTP) Home Delivery Services for Clinical Trial Materials provides an in-depth look at reasons to consider...
Piramal Healthcare Ltd | Recorded the 24-May-2013 | Webinar
With the recent approvals of brentuximab vedotin (Adcetris) and ado-trastuzumab emtansine (Kadcyla,T-DM1), antibody–drug conjugates (ADCs)are a rapidly...
Import/export of biological samples from ChinaChina: Large Pharma Reverse LogisticsA Common Issue: Destruction of Drug in TaiwanJ-GMP: How is GMP different...
Through real-world examples, webinar participants learn strategies for choosing appropriate outcome measures, methods for analysis and randomization, and...
2013 Industry trends driving the scientific, logistical and regulatory complexity of supply chain industryImplement clinical development methodologies...
What are the regulators telling us?Dealing with a non-harmonized, multi-agency, global challenge. Monsters Vs, AliensHow to navigate the maze of import...
Marken: Global Life Science Supply Chain Solutions | Recorded the 20-Mar-2013 | Webinar
How to determine if a depot or direct to site shipments are more efficientCalculation based on a case studyHow to avoid delays and assure that your shipments...
The Industry’s changing approach to clinical data monitoring requires the tools and team structure to effectively plan and execute risk-based monitoring....
Baxter BioPharma Solutions | Recorded the 12-Sep-2012 | Webinar
This webinar will discuss development of design spaces for lyophilized pharmaceutical products in the context of the Quality by Design regulatory paradigm. ...
The development of therapeutics for personalized medicine leverages many of the advantages of the legislation conferred upon orphan products. New products...
The Prescription Drug and User Fee Act (PDUFA) IV will expire in September 2012. A new version of this legislation, PDUFA V, is expected in the coming...
Analgesic clinical trials often fail, even when we know the drugs work. Join Lynn King and Karen Kesler as they share real-world solutions for trial design,...
Millipore Corporation | Recorded the 13-Dec-2011 | Webinar
Flow cytometry is a versatile, multiparameter technique with many applications including pharmacodynamic analysis for clinical studies.We invite you to...
Millipore Corporation | Recorded the 11-Oct-2011 | Webinar
High throughput screening of antibody pairs to determine best binding characteristics, and their selection for development of immunoassays. Identification...
