Session 1: Wednesday, November 9, 2022 at 8am EST |1pm GMT | 2pm CET Session 2: Wednesday, November 9, 2022 at 2pm EST |1pm CST | 11am PST Join Merck, IPS, and Synergis Software on November 9th to learn how Merck is leveraging the Synergis Adept engineering document management platform to address these issues while driving standards and best practices.
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 October 27, 2022 at 11am ET | 10am CT | 8am PT When it comes to freely accessing and sharing lab data, there’s a lot working against you out there. To create infrastructure that truly mobilizes your data and modernizes your lab, you need a new kind of solution.
Thursday, October 20, 2022 at 11 AM EDT | 10 AM CDT | 8 AM PDT It’s no secret that hybrid and decentralized trials (DCT) are here to stay. Make sure your organization is ready for the shift towards clinical trials that put patients first.
Tuesday, October 11, 2022 at 11am EDT | 10am CDT | 8am PDT Learn how integrated formulation and clinical manufacturing expertise, as well as strategic partnerships between CDMOs and CROs, can help achieve flexible and efficient first-in-human studies, fast development of challenging molecules, and reduced clinical development timelines and costs, all while increasing success rates.
Wednesday, October 5, 2022 at 11:30am ET | 10:30am CT | 9:30am PT Developing an Analytical Framework for Success using a chemically modified mRNA can be compared with those for traditional biologics,. As such, it’s especially important that control on quality and consistency is maintained to ensure well characterized drug substance.
Tuesday, October 4, 2022 at 11am CDT |12pm EDT | 9am PDT Is developing formulations of highly lipophilic compounds worth the effort? With today’s excipients and technologies, the answer is a definite yes. This presentation will showcase the issues presented by lipophilic compounds and ways to address them.
Thu, Sep 29, 2022 11:00 AM EDT Are your biological samples held up in customs? Understand how to import and export biological samples with efficiency in this webcast.
Tue, Sep 27, 2022 11:00 AM EDT In this webinar, failure modes that can occur on a perfectly sealed container will be discussed along with how to determine if a CCIT failure is a true container leak or something else
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.
Thursday, September 8, 2022 at 11am EDT; 4pm GMT; 5pm CEST This webinar will highlight the new solubility enhancing Dispersome® technology, which is based on the amorphous stabilization of a given drug using the protein beta-lactoglobulin (BLG) as novel pharmaceutical excipient. Several relevant case studies are presented to showcase the potential of this new technology. Subsequently, the webinar provides a roadmap on how these formulations can be manufactured on a commercial scale. The webinar will also cover the manufacturing of the formulations.
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.
Thursday, July 21st, 2022 at 11am EDT|8am PDT|4pm BST|5pm CEST Learn about the use of molecular spectroscopy techniques – transmission Raman spectroscopy (TRS) and laser direct infrared (LDIR) – for solid-state analysis in pharmaceutical formulation development.
Thursday, July 14th, 2022 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST Join us to learn approaches for the accurate determination of mutagenic azido, NDSRI, and nitrosamine impurities in drug substances and products using LC–MS/MS.
Tuesday, July 12th, 2022 at 11am EDT|8am PDT|4pm BST|5pm CEST Dr. Meike Römer from Grünenthal Pharma, Germany, presents the company’s approach for the evaluation and implementation of transmission Raman spectroscopy for pharmaceutical content uniformity testing.
Thursday June 30, 2022 at 11am ET | 10am CT | 8am PT Cell and gene therapy (CGT) and antibody-drug conjugate (ADC) developers and manufacturers discuss factors that could influence organizations to pursue specific biomolecules for development. Pharmaceutical Technology editors interview experts in CGTs and ADCs in this episode of the Drug Digest video series.
Thursday, June 23, 2022 at 10am ET | 3pm BST | 4pm CEST Join us on June 23 to learn about QC Analysis of Oligonucleotide Therapeutics. One Platform Method for Determining Identity, Purity, and Quantity.
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
Wednesday, May 25, 2022 at 11am EDT|8am PDT|5pm CEST|4pm BST In the last few years, the issuance of the ISO 10993-18:2020 medical device guidance and several high-profile publications and round robin studies have resulted in the FDA increasing scrutiny of E&L analyses for both drugs and devices. Join our panel of industry experts to discuss these changes and to learn the direction E&L studies may take in the future.
Wednesday, May 18th, 2022 at 3pm BST | 10am EDT | 4pm CEST | 7am PDT Join global industry and regulatory experts as they discuss current E&L hot topics on pharmaceuticals, biopharmaceuticals and medical devices.
Thursday April 28, 2022 at 11am ET | 10am CT | 8am PT In this new video series, Drug Digest, the Pharmaceutical Technology editors examine the topic of emerging therapies in more detail, covering subjects such as the challenges of scale, the potential benefits of drug delivery innovation, importance of early analytical studies, the evolution of the regulatory landscape, and differences between regional regulatory requirements. Join the editors as they speak with experts from Regulatory Compliance Associates (RCA), the European Confederation of Pharmaceutical Entrepreneurs (EUCOPE), and others.
April 27th, 2022 at 11am EDT | 8am PDT | 3pm GMT | 10am CDT Transform Data into Scientific Discoveries. PerkinElmer’s World Class eNotebook and Scitara DLX Live Demo! Signaling the Future with True Informatics Data Mobility. Watch our live demonstration on how to achieve true data mobility!
Thursday, April 21, 2022 at 11am ET | 4pm GMT | 5pm CET This webinar will discuss risk mitigation strategies used to address common challenges during spray dried powder development and give insight into the impact of spray drying on powder properties in terms of manufacturability and downstream processability.
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.
Thursday, April 14, 2022 at 11 AM EDT | 8 AM PST | 3 PM GMT Suspension formulations – simple or complex? As with many things the answer is “it depends”. This presentation will address the development of suspensions from simple, initial animal study products through complex commercial products.
Thursday, March, 24, 2022 at 4:00pm GMT | 12:00pm EST | 5:00pm CEST From lyophilization to particle engineering. Learn how spray drying can improve solid-form isolation of biopharmaceuticals and expedite your development pipeline, throughput, and therapeutic delivery.
Wednesday, March 23, 2022 at 11am EST | 10am CST | 8am PST The goal of this webinar is to provide clarity on what the upcoming computer software assurance (CSA) guidance means for life sciences companies and what they can do to start preparing. Leading experts from Biogen, Vertex, Alkermes and Verista will share their advice and best practices to ensure a successful rollout.
Wednesday, March 16, 2022 at 11 am EST | 10am CST | 8am PST What will audits and inspections look like once COVID 19 has passed? Attend this webinar to learn how the FDA is approaching inspectional activities depending on the industry.
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.
Tuesday, March 1st 2022, at 11 am EST Making oral solid dosage forms conveniently, using galenIQ™ - the sweet-tasting filler binder.
