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Best Practices for Meeting and Exceeding Regulatory Standards in Primary Packaging USP and
July 22nd 2020Interested in learning more about the regulatory requirements for elastomeric components in parenteral drug packaging? Sign up for the July 22 webcast on “Best Practices for Meeting and Exceeding Regulatory Standards in Primary Packaging USP and ” . This webcast is part of a series focusing on “The Path to Patient Safety – Addressing Industry Concerns and Solutions for Primary Packaging Component Selection.” Live: Part II: Wednesday, Jul. 22, 2020 at 10am EDT | 9am CDT | 3pm BST | 4pm CEST On demand available after airing until Jul. 22, 2021 Register free
Effective Imaging for Identification and Sizing API Domains
July 21st 2020Combining FTIR and Raman spectroscopy provides the insight needed to ensure appropriate distribution and concentration of APIs within tablets. Watch this webcast to learn more. Live: Tuesday, Jul. 21, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jul. 21, 2021 Register free
Expedite Regulated Documents in the Era of COVID-19: From Development to Trials and Manufacturing
July 15th 2020Technology is more critical than ever to help you keep your clinical trials on track during the era of COVID-19. Gain best practices about how to empower your remote workforce, get critical regulated documents electronically signed compliantly, and to create a safe and flexible remote patient-centric experience. Live: Wednesday, Jul. 15, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jul. 15, 2021. Register free
How to Choose the Right Approach to Enhance Drug Solubility
June 25th 2020What is the correct approach for formulation development of poorly soluble NCEs? Dr. Umesh Barabde, director and operations head, Pharmaceutical Development Services, and Dr. Vishakh Kharat, director, analytical research, Pharmaceutical Development Services, both at Piramal Pharma Solutions discuss classic and specialized techniques to enhance solubility. Live: Thursday, Jun. 25, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jun. 25, 2021 Register free
Dry Powder Inhalers: Key Considerations for Combination Product Development
June 24th 2020Dry powder inhalers (DPIs) are an important delivery technology for inhaled medicines in both respiratory and non-respiratory disease areas. Andreas Meliniotis, director of device development at Vectura, helps navigate the complex area of DPI product development and highlights the key considerations for both novel- and generic-drug programs. Live: Wednesday, Jun. 24, 2020 at 11am EDT |8am PDT |4pm BST |5pm CEST On demand available after final airing Jun. 24, 2021 Register free
Instrument Systems Take on Burden of Compliance
June 23rd 2020Want to be sure your systems and processes are compliant? Learn how two enable 21 CFR Part 11 in the lab with compliant workflows and consistent testing. Be confident in your analyses! Live: Tuesday, Jun. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after final airing Jun. 23, 2021 Register free
Specialized Clinical Services for Complex Clinical Studies
June 23rd 2020This webinar will review Lonza’s integrated clinical supply services inclusive of manufacturing, primary and secondary packaging, kitting, and distribution with special emphasis on complex clinical studies and direct-to-patient shipping. Live: Tuesday, Jun. 23, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Jun. 23, 2021 Register free
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
