Webcasts
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How Digital Lab Assistants Can Improve GMP Data Integrity
June 22nd 2020Recording and tracking data streams in real-time, within GMP facilities is challenging. Learn how voice-powered digital lab assistants provide a solution by directly communicating with lab instruments and by automatically transcribing voice notes from staff to ensure data can be attributed to staff members via user identification, automatic timestamps, and electronic signatures. Live: Monday, Jun. 22, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 22, 2021 Register free
Preformulation of Small Molecule Drugs
June 18th 2020Preformulation studies play a significant role in developing approaches to analytical and formulation development based on the physicochemical properties of small-molecule pharmaceuticals. This webinar will provide insights into the preformulation phase of drug development and will illustrate common issues encountered. Live: Thursday, Jun. 18, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jun. 18, 2021 Register free
Comprehensive Analysis into Disintegration Mechanisms: How Reliable Are Textbook Recommendations?
June 10th 2020When formulating a tablet, the solubility of the tablet matrix is often used as the sole criteria for disintegrant selection. Most formulators tend to select swelling-type disintegrants for insoluble matrices and wicking-type disintegrants for soluble matrices. This webcast will present an in-depth analysis of the effects of disintegration mechanisms, pH of test media, matrix plasticity, tablet hydrophobicity, and storage effects on the disintegration behavior. Live: Wednesday, Jun. 10, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 10, 2021 Register free
Discovery, Formulation, and Performance of Self-Emulsifying Drug Delivery Systems (SEDDS)
June 4th 2020Self-emulsifying drug delivery systems, or SEDDS, are arguably the most successful technology in the market today for taking poorly water-soluble APIs and turning them into bioavailable formulations. But where do you start? Learn about the physical chemistry of these systems, discuss testing options, and uncover 10 ready-to-use formulations to be used for your next project. Live: Thursday June 4, 2020 at 11am EDT| 8am PDT| 4pm BST| 5pm CEST On Demand: available after airing until June 4, 2021 Register free
Excipient Science in Protecting Moisture Sensitive Drugs
June 3rd 2020Don’t just rely on packaging to protect drug products from moisture. In this webcast, discover how to develop more stable formulations by selecting the right excipients for use with moisture-sensitive drugs, and in doing so, reduce the risk of degradants and impurities. Live: Asia Pacific: Wednesday, Jun. 3, 2020 at 12pm IST | 2:30pm CST | 3:30pm JST US and Europe: Wednesday, Jun. 3, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Jun. 3, 2021 Register free
Adopting a Data-Centric Quality Mindset
May 28th 2020In this exclusive webcast, MasterControl’s Product Management Director Sue Marchant examines why document dependency has become a hindrance to manufacturers and how companies can successfully chart a clear path to digital and data maturity. She also explains the drivers behind the industry’s shift away from document-centered quality management and explores trends relating to digital quality management. Live: Thursday, May 28, 2020 at 2pm EDT| 1pm CDT| 11am PDT On demand available after airing until May 28, 2021 Register free
Practical Considerations for Bringing Drug Candidates to Phase I Clinical Trial
May 27th 2020Looking for the right approach to advance your small molecule drug candidate? Philip Jones from MD Anderson Cancer Center shares thoughts on how to bring drug candidates to Phase I clinical trials. Live: Wednesday, May 27, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 27, 2021 Register free
Clinical to Commercialization: The Case for Design/Build Modular Facilities
May 27th 2020Learn how biopharmaceutical development and production can be more efficient by using modular technology. Live: Wednesday, May 27, 2020 at 2pm EDT | 1pm CDT | 11am PDT On demand available after airing until May 27, 2021 Register free
Editors’ Series: Strategies for Designing Adaptable, Resilient Bio/Pharma Facilities
May 26th 2020The COVID-19 pandemic should prompt bio/pharma facilities to assess how the potential spread of the virus may impact different areas of development and manufacturing facilities, employees, visitors, and product. Learn about strategies for evaluating practices at existing facilities and options for designing new facilities that can accommodate future needs, including flexibility requirements and any emerging threats. Live: Tuesday, May 26, 2020 at 2 pm EDT| 1pm CDT| 11am PDT On demand available after airing until May 26, 2021 Register free
Ensuring Integrity of Drug Formulation from Development to QC
May 21st 2020Learn how to reduce the number of steps and resources needed to assure chemical and structural integrity throughout drug development process. See where efficiencies can be gained in analytical methods development and transfer to QC and manufacturing while staying compliant with cGxP. Thursday, May 21, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after final airing May 21, 2021 Register free
When Drug Meets Device: How to Assess Compatibility
May 19th 2020For drug-device combination products, the compatibility of the drug and device components requires analysis of many factors. In this webcast, learn about regulations and drug-device compatibility assessment steps that are necessary to protect patients. Live: Tuesday, May 19, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 19, 2021.
Bulletproof your Supply Chain: Hope for the Best, Prepare for the Worst
May 18th 2020Learn from the experts on how to best combine supply-chain management and logistics expertise to build a nimble and efficient operation that can help to mitigate risks such as those brought on by the COVID-19 pandemic. Live: Monday, May 18, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing May 18, 2021 Register free
OTC Trends, Monograph Reform, and Innovation
May 5th 2020Gain insight from Nicholas Hall, the Consumer Healthcare Products Association, and Catalent into the performance of the OTC market, some of the innovation trends and opportunities that are emerging, and the impact of OTC monograph reform on future developments. Live: Tuesday, May 5, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until May 5, 2021 Register free
Ensuring the Continuous Supply of Quality Drug Products During Uncertain Times
April 28th 2020The global coronavirus pandemic has tested the abilities of bio/pharmaceutical companies to develop new therapies and maintain-or even accelerate-production of existing drugs. In this webcast, experts will discuss business continuity practices, regulatory compliance, and supply chain management under current-or future-emergency conditions. Live: Tuesday, Apr. 28, 2020 at 11 am EDT | 10 am CDT | 8 am PDT On Demand: available after airing until Apr. 28, 2021 Register free
On-Dose Authentication to Safeguard Patients and Uphold Brand Integrity
April 23rd 2020Don’t just rely on packaging to deter the counterfeiting of your drug products. In this webcast you will discover how patient-centric, on-dose authentication can protect products and mitigate counterfeiting and product diversion. Just imagine uniquely encoded micro taggants applied to your product and being able to authenticate right through the supply chain to the patient level…..now that’s smart ! Live: Thursday, Apr. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 23, 2021 Register free
Leveraging Digital Assistance to Address Oral Solid Dosage Formulation Challenges
April 21st 2020Looking to eliminate trial and error in the early stages of formulation development? Learn how the ZoomLab™ Virtual Formulation Assistant, can predict and optimize an oral solid dosage drug formulation more efficiently than with traditional approaches. Live: Tuesday, Apr. 21, 2020 at 9am EDT | 2pm BST | 3pm CEST On Demand: available after airing until Apr. 21, 2021 Register free
Integrated Pre-Formulation Studies for Fast Advancement of Drug Candidates to Human Clinical Studies
April 15th 2020Looking for a fast pathway to an investigational new drug application (IND) for your new drug candidates? This webcast will discuss strategies to select the most developable molecules and quickly develop an IND-ready formulation within 8–12 weeks using real-world case studies. Live: Wednesday, April 15, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 15, 2021 Register free
Oral Peptide Delivery Utilizing Specialized Encapsulation Technologies
April 1st 2020This webcast will cover physicochemical requirements and biological oral delivery barriers for peptides. Learn innovative approaches to derisk pharmaceutical development and increase the success rate of the first in human trials. Live: Wednesday, Apr. 1, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 1, 2021 Register free
Optimizing Equipment Availability for Capsule Fillers
March 24th 2020Learn what the common equipment bottlenecks are and how engineering developments can maximize equipment availability. Experts will provide insight into how to minimize cycle, set-up, and changeover times and how to define optimal parameters for each process step. Live: Tuesday, Mar. 24, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 24, 2021 Register free
Sterile Filling Challenges for Early-Phase Product Development
March 19th 2020Learn techniques on getting your drug product to market faster and more efficiently. Live: Thursday, Mar. 19, 2020 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET On demand available after airing until Mar. 19, 2021 Register free
Headspace Gas Ingress Testing for Container Closure Integrity
March 18th 2020Imagine a blue dye test that uses a tracer gas in place of the dye. Headspace gas ingress testing is a robust detection method of critical leaks. Drug developers considering an upgrade to blue dye testing can learn more about this test method in this webcast. Live: Wednesday, Mar. 18, 2020 at 11:30am EDT | 8:30am PDT | 3:30pm GMT | 4:30pm CET On Demand: available after airing until Mar. 18, 2021. Register free: http://www.pharmtech.com/pt_w/closure
