Webcasts

Oct 16, 2018
Sponsored Content
Although they may be chemically derived, complex generic APIs present more complex analytical challenges than conventional “small molecule” APIs in demonstrating sameness. Learn how to optimize analytical strategies for these complex molecules.

Live: Tuesday, 16 October, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 16 October, 2019.

Register free: http://www.pharmtech.com/pt_w/api
Sep 26, 2018
Sponsored Content
Next-generation biologics are starting to dominate early phase pipelines. The complex nature of these molecules can mean that they are difficult to express and require new tools to achieve economically viable concentrations and clinically relevant critical quality attributes. In this webcast, learn about new tools that are now available and others that are currently in development.

Live: Wednesday, 26 September, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 26 September, 2019.

Register free: http://www.pharmtech.com/pt_w/proteins
Aug 21, 2018
Sponsored Content
Are you interested to learn what makes a successful method transfer to a quality control team? And, would you like to learn how to gain efficiency to continually deliver on customer expectations? Join our webcast to hear recommendations from Beccy Bell, Analytical Manager at Broughton Laboratories, to gain insights.

Live: Tuesday, 21 August, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 21 August, 2019.

Register free: http://www.chromatographyonline.com/lcgc_w/journey
Aug 07, 2018
Sponsored Content
Clinical trial protocol design can have a significant impact on the commercial drug sourcing strategy for a study requiring comparators. Learn the appropriate level of detail to include in the study protocol to help avoid common sourcing issues later on. Hear why early input into the protocol design can potentially impact the costs, timelines, operational complexity, and overall risk incurred when sourcing comparators.

Live: Tuesday, 7 August, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 7 August, 2019.

Register free: http://www.pharmtech.com/pt_w/reducing
Jul 31, 2018
Sponsored Content
Learn about a development approach can expedite delivering specialized therapies to clinic using a fast and flexible options for mammalian cell line development and process development; integrated drug substance, drug product, and clinical trial logistics solutions; optimized dosage form selection; and right-sized filling lines for early development.

Live: Tuesday, 31 July, 2018 at 10 am EDT | 1500 BST | 1600 CEST / On Demand available after airing until 31 July, 2019.

Register free: http://www.pharmtech.com/pt_w/building
Jul 25, 2018
Sponsored Content
Join expert Matthew Jones as he talks about how a well-designed crystallization process and sufficient knowledge of the solid-state properties of a drug substance are essential to ensure high product purity and that the desired crystal modification is delivered consistently.

Live: Wednesday, 25 July, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST

On Demand available after airing until 25 July, 2019.

Register free: http://www.pharmtech.com/pt_w/crystallization
Jul 24, 2018
Sponsored Content
Join Dr. Frank Steiner and Dr. Dan Bach Kristensen as they take you on a journey of UHPLC method transfer; you may be surprised how short it can be. Learn about the critical parameters for successful method transfer between the same and differing UHPLC systems and hear about real-world examples of method transfer based on complex biotherapeutic separations.

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

Register free: http://www.chromatographyonline.com/lcgc_w/journey
Jul 18, 2018
Sponsored Content
Drug product development for highly potent APIs (HPAPIs) can be challenging. Complications with the interface between operations in drug substance and drug product handling can result in increased program complexity and cost. Join this discussion on the development, rapid scaling, and commercial production of HPAPI drug substance, as well as integrated containment requirements for particle engineering and drug product.

Live: Wednesday, 18 July, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 18 July, 2019.

Register free: http://www.pharmtech.com/pt_w/potent
Jul 12, 2018
Sponsored Content
You may have a promising drug, but if all patient groups won’t take it, its benefits can be lost. Effective, patient-centric formulation strategies are required to ensure compliance, especially for pediatric medications.

Solid oral dosage forms are becoming preferred to liquids for children’s medicines, but also in treatments for geriatric and other hard-to-dose patient groups. Multiparticulate technologies offer an effective format for challenging patient populations, because of their ease of formulation, dose flexibility, suitability for concealing taste and modifying release, ease of administration and robust stability.

Live: Thursday, 12 July, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 12 July, 2019.

Register free: http://www.pharmtech.com/pt_w/pediatric
Jun 27, 2018
Sponsored Content
First-generation antibody drug conjugates (ADCs) have development challenges. In this webcast, Lonza Pharma & Biotech provides insight on tools and techniques for engineering a better ADC and developing a successful process fit for production and scale-up. Case studies will be presented.

Live: Wednesday, 27 June, 2018 at 11 am EDT | 8 am PDT | 1600 BST | 1700 CEST / On Demand available after airing until 27 June, 2019.

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