Apr 24, 2018
Sponsored Content
As companies transition products from early- to late-phase development, there are key considerations that need to be determined before selecting a partner. This webcast will discuss key strategies a company can take to streamline the development process while addressing both early and late phase needs.

Live: Tuesday, 24 April, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 24 April, 2019.

Register free: http://www.pharmtech.com/pt_w/design
Mar 28, 2018
Sponsored Content
In this webcast, participants will learn about best practices for spray-dried dispersion formulation development in the areas of manufacturability, performance, and stability.

Live: Wednesday, 28 March, 2018 at 11 am EDT | 10 am CDT | 1600 BST | 1700 CEST / On Demand available after airing until 28 March, 2019.

Register free: http://www.pharmtech.com/pt_w/spray
Mar 15, 2018
Sponsored Content
Want to reduce risks in the single largest raw material ingredient used in Pharma: water? Learn about regulatory requirements, and how to apply online water bioburden analyzers and real-time process control techniques to see the big picture.

Live: Thursday, 15 March, 2018 at 11 am EDT | 10 am CDT | 1500 GMT | 1600 CET / On Demand available after airing until 15 March, 2019.

Register free: http://www.pharmtech.com/pt_w/purity
Mar 14, 2018
Sponsored Content
Improve the success rate in drug discovery and development by incorporating early developability assessment into a therapeutic candidate development strategy. Lonza’s Yvette Stallwood will discuss how best to use these tools for a developability assessment and to create a de-risking strategy for therapeutic candidates.

Live: Wednesday, 14 March, 2018 at 11 am EDT | 10 am CDT | 1500 GMT | 1600 CET / On Demand available after airing until 14 March, 2019.

Register free: http://www.pharmtech.com/pt_w/therapeutic
Mar 07, 2018
Sponsored Content
Is the goal of Quality compliance or performance? Sign up for this webcast to learn how to accomplish both!

Live: Wednesday, March 7, 2018 | 11 am EST | 10 am CST | 8 am PST / On Demand available after airing until March 7, 2019.

Register free: http://www.pharmtech.com/pt_w/goals
Feb 15, 2018
Sponsored Content
Learn analysis techniques for evaluating product integrity risk for new drug products including potential for falsification, diversion, and other risks that impact product liability, dilute revenue, and consumer safety and trust. Review the conditional decision process for reducing these threats and if an “on-product” verification solution is right for your drug product. In addition, learn the latest advancements in on-dose technologies including what product intelligence is revealed and hear an expert’s experience in evaluating use for specific products and markets.

Live: Thursday, Feb., 15, 2018 | 1 pm EST | 12 pm CST | 10 am PST / On Demand available after airing until Feb., 15, 2019.

Dec 12, 2017
Sponsored Content
Join this webcast to gain an understanding of the guidelines, testing requirements, and analytical approaches for complying with the USP. Discussion will include steps to perform risk assessments, and testing requirements for oral, parenteral, and inhaled products. A Q&A session will allow a deeper dive into specific needs.

Live: Tuesday, 12 Dec., 2017 | 11 am EST | 8 am PST | 1600 GMT | 1700 CET / On Demand available after airing until 12 Dec., 2018.

Register free: http://www.pharmtech.com/pt_w/assessment
Dec 07, 2017
Sponsored Content
By Lonza
The road to a successful BLA submission can be a long and complex journey. Join Lonza’s Jason Osman and John McGuire as they share their roadmap for making your expedition to BLA submission a success.

Live: Thursday, Dec. 7, 2017 | 12 pm EST | 11 am CST | 9 am PST / On Demand available after airing until Dec. 7, 2018.

Register free: http://www.pharmtech.com/pt_w/biologic
Nov 28, 2017
Sponsored Content
Learn how chemists and engineers, working together before pilot-plant activity, can de-risk chemical process development and assure first-time-right process scale-up and transfer. Understand how the Process Engineering Laboratory can optimize QBD approaches and efficient chemical manufacturing.

Live: Tuesday, Nov. 28, 2017 | 11 am EST | 10 am CST | 8 am PST / On Demand available after airing until Nov. 28, 2018.

Register free: http://www.pharmtech.com/pt_w/chemical
Nov 09, 2017
Sponsored Content
This webcast will examine the key areas of expertise that the comparator sourcing specialist and clinical supply manager each contribute to the development of a comprehensive sourcing plan. We will discuss how practical experience and having strong industry relationships not only impact the sourcing plan but can impact the willingness of innovators and downstream suppliers to make the requested product available as well.

Live: Thursday, 9 Nov., 2017 | 11 am EST | 8 am PST | 1600 GMT | 1700 CET/ On Demand available after airing until 9 Nov., 2018.

Register free: http://www.pharmtech.com/pt_w/sourcing
lorem ipsum