Webcasts

May 30, 2018
Sponsored Content
By SCHOTT
The rise of biologics comes with a challenge: These highly sensitive and complex drugs require special packaging to ensure drug stability as well as safe administration for the patient. This free webcast offers a detailed analysis of the market and packaging innovations for biopharmaceuticals.

Live: Wednesday, 30 May, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 30 May, 2019.

Register free: http://www.pharmtech.com/pt_w/biologics
May 24, 2018
Sponsored Content
With the mounting external pressures and security of supply concerns, is Pharma ready to lead the supply chain revolution?

The future of Pharma is instantaneous feedback up-and-down the supply chain. Vendor Managed Inventory (VMI) coupled with Electronic Data Interchange (EDI) integrates your forecast into your vendor’s production plan, preparing them for the pace of the future.

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

Register free: http://www.pharmtech.com/pt_w/revolution
Apr 25, 2018
Sponsored Content
Review the specific challenges manufacturing organizations are facing today and learn about ways to leverage technology to address regulatory needs and economic concerns. Manufacturing, operations, and IT professionals from contract manufacturing organization (CMO), drug sponsors, and joint manufacturing partners will find this webcast highly informative.

Live: Wednesday, 25 April, 2018 at 10 am EDT | 9 am CDT | 1500 BST | 1600 CEST / On Demand available after airing until 25 April, 2019.

Register free: http://www.pharmtech.com/pt_w/network
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
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