Webcasts: Manufacturing

Webinar Date/Time: Friday, May 19, 2023 at 11am EDT| 10am CDT | 8am PDT

Webinar Date/Time: Friday, April 28, 2023 at 11am EDT | 10am CDT | 8am PDT

Webinar Date/Time: Tue, May 23, 2023 11:00 AM EDT

Webinar Date/Time: Tue, Apr 25, 2023 11:00 AM EDT

Webinar Date/Time: Tue, Apr 18, 2023 11:00 AM EDT

Webinar Date/Time: Tuesday, April 4th, 2023 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

Webinar Date/Time: Thu, Apr 6, 2023 11:00 AM EDT

Webinar Date/Time: Thu, Mar 23, 2023 11:00 AM EDT

Webinar Date/Time: Wed, Mar 1, 2023 11:00 AM EST

Webinar Date/Time: Thu, Feb 23, 2023 11:00 AM EST

Webinar Date/Time: Tuesday, February 28th, 2023 at 11am EST | 8am PST | 4pm GMT | 5pm CET

Webinar Date/Time: Thursday February 24, 2023 at 11am EST | 10am CST | 8am PST

Webinar Date/Time: Thu, Oct 27, 2022 11:00 AM EDT

Webinar Date/Time: Tue, Jan 31, 2023 11:00 AM EST

Webinar Date/Time: Thursday January 19, 2023 at 11am EST | 10am CST | 8am PST

Webinar Date/Time: Thursday, December 8, 2022 at 11am EST | 10am CST | 8 am PST

Webinar Date/Time: Mon, Dec 12, 2022 11:00 AM EST

Webinar Date/Time: Wednesday, November 30, 2022 at 11 am ET | 10 am CT | 8 am PT

Tuesday, November 8, 2022 at 11 am EDT | 10am CDT | 8am PDTThis webinar will provide a detailed look at successful procedures for developing effective viral clearance and purification strategies to improve mAbs downstream process efficiency through enhanced engineering of a novel Protein A resin, combined with selective additives in key process steps. The webinar will include details on new techniques and recommendations for optimizing process steps, to help reduce costs and process time and increase downstream yield.

Thursday, September 28, 2022 at 11am ET | 10am CT | 8am PT Learn the key benefits of continuous OSD production as well as the importance of authenticating OSD products at the dose-level with experts from Syntegon and Colorcon in this episode of the PharmTech Drug Digest Video Series.

Thursday, September 15, 2022 at 4pm ET | 3pm CT | 1pm PT Partnering with an experienced CDMO can support drug developers’ manufacturing needs and allow them to focus on the core of their developments.

Thu, Aug 25, 2022 11:00 AM EDT Pharmaceutical Technology editors interview aseptic and sterilization experts from Watson-Marlow Fluid Technology Solutions and Cherwell—diving into sterilization, aseptic processing, and the revised EU GMP Annex 1 guidance.

Tuesday, June 14th, 2022 at 7:30am PDT | 9:30am CDT | 10:30am EDT Join Lonza and Quench Medical in a joint discussion about process engineering for the respiratory delivery of gemcitabine to treat lung cancer

Tuesday, April, 19, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Be assured they have the most uptime possible to keep production on track! Register for this webinar to learn how advanced technologies can help ensure complete asset integrity, guarantee optimal facility conditions (such as temperature, humidity, and vibrations), predict the expected lifespan of equipment and track the energy an asset has consumed and its CO2 emissions.

Wednesday March 2, 2022 at 11am EST | 4pm GMT | 5pm CET Compounds that are poorly soluble in water are still prevalent in the pharmaceutical industry drug development pipeline. Enabling technologies such as lipid-based formulations (LBF) and amorphous solid dispersions (ASDs) can address these bioavailability limitations, enabling the creation of effective drug products.

Monday, February, 28, 2022 at 9am EST | 8am CST | 6am PST Realizing benefits from Smart Manufacturing technologies doesn’t have to be long-term prospect. Solve today’s manufacturing challenges while laying the foundation for tomorrow’s plant.

Wednesday, February 16, 2022 at 9 AM EST | 6 AM PST | 2PM GMT | 3 PM CET & 11AM EST | 8AM PST | 4PM GMT | 5PM CET How are you approaching Pharma 4.0 and the QC Lab of the future with automation? Join us for an informative Webinar on the benefits of end-to-end integration with LIMS and QC Micro automation.

Monday December 20, 2021 at 11am EST | 10am CST | 8am PST Pharmaceutical manufacturers are under increasing pressure to fast-track technological innovation while remaining compliant. What are the correct steps to reaching operational intelligence with end-to-end data integrity?