Datwyler

When it comes to injectable drugs, quality considerations are of utmost importance to ensure patient safety and efficacy. In this webinar, industry experts will introduce the latest quality advancements and explain how these innovations are not only making medications cleaner and safer but are also promoting sustainability in the healthcare industry.

https://www.pharmtech.com/pt_w/injectable-drug-quality

When it comes to injectable drugs, quality considerations are of utmost importance to ensure patient safety and efficacy. The manufacturing process must adhere to guidelines and regulations to maintain purity, potency, and sterility and rigorous testing and quality control should detect any potential impurities or defects before market release. In this webinar, industry experts will introduce the latest quality advancements and explain how these innovations are not only making medications cleaner and safer but are also promoting sustainability in the healthcare industry.

Discover essential factors to consider when packaging injectable drugs for optimal quality

Explore the advancements in pharmaceutical packaging that are revolutionizing quality standards

Gain insights into the strategies employed by packaging suppliers to mitigate risks and ensure top-notch quality

Quality/regulatory personnel in parenteral drug delivery

Formulation scientists and packaging engineers

Device development engineers and managers

Technical functions surrounding drug delivery systems


Global Customer Quality Officer
Datwyler

Ankit Kumar, a seasoned professional with over 14 years of experience in the industry, has been a vital force at Datwyler since April 2021. With a diverse career spanning different domains and global roles, Ankit brings a wealth of experience to the table.

In his current role, Ankit is at the forefront of Datwyler's commitment to total quality. Managing key global processes such as change management, quality agreements, and audit management, Ankit is instrumental in driving a quality culture throughout the organization. His headship extends to conducting global quality trainings, ensuring that the principles of excellence are ingrained at every level of the company.




Quality Key Account Manager
Datwyler

Barbara Santambrogio joined Datwyler in 2011 and has held different positions in the Quality Assurance department, ending as Quality Assurance Manager for the two Italian sites. In April 2021, she took over the role as Quality Key Account Manager for selected global/strategic customers. Before joining the Datwyler organization, Barbara gained experience in the pharma industry working for two pharmaceutical companies. Barbara also has two degrees in Pharmaceutical and Chemistry technology and in Pharmacy.

Webcasts

Webinar Date/Time: Tue, Nov 5, 2024 9:00 AM EST


  Advancing Injectable Drug Quality: Innovations, Compliance, and Sustainability in the Healthcare Industry

How pharmaceutical packaging is designed to prevent leakage and contamination, and ensure the quality of injectable drugs.

https://www.pharmtech.com/pt_w/sealed-for-safety

Container closure integrity (CCI) plays a vital role in the packaging of injectable drugs. It is crucial for guaranteeing the safety and effectiveness of these medications, as any compromise in the container's seal can result in microbial contamination or a decrease in drug potency. Join us for an insightful webinar where industry experts will delve into the intricacies of pharmaceutical packaging, uncovering how it is meticulously designed to prevent leakage and contamination, and ensure the utmost quality of injectable drugs.

Discover the essential factors of CCI and the testing methods utilized to mitigate potential risks

Learn how to assess CCI and ensure the utmost quality of injectable drugs

Discover the advantages of collaborating with packaging suppliers to create a holistic packaging solution for injectable drug developers


Technical and Scientific Expert
Datwyler

 is currently a Technical and Scientific Expert at Datwyler and brings a breadth of experience to support for Datwyler’s customers on their product development needs. He previously worked in a commercial development role at Becton Dickinson (BD) providing pharmaceutical customers with consultation on BD products, services, and solutions to meet their development timeline needs. Prior to BD, he was a combination product R&D engineer at AstraZeneca responsible for managing technical aspects of device development, such as user needs, test method development, design verification, and design validation. Yitian holds a M.Eng in Biomedical Engineering from Cornell University and a B.S. in Biomedical Engineering from Georgia Tech.

Webinar Date/Time: Wed, Oct 2, 2024 9:00 AM EDT



Sealed for Safety: A Deep Dive into Container Closure Integrity

To engineer pharmaceutical packaging components, a deep understanding of an injectable drug's requirements and specifications, as well as its manufacturing and filling environments is crucial. In this webinar, industry experts will delve into the engineering requirements and considerations necessary to design, manufacture, and supply packaging components that safeguard drug integrity, prevent contamination, and above all, prioritize patient safety.

https://www.pharmtech.com/pt_w/discovery-to-delivery

Without the appropriate packaging components, even the most effective injectable drug cannot achieve success. To engineer these components, a deep understanding of the drug's requirements and specifications, as well as the manufacturing and filling environments, is crucial. Additionally, considering the needs of the end-users is vital. In this webinar, industry experts will delve into the engineering requirements and considerations necessary to design, manufacture, and supply packaging components that safeguard drug integrity, prevent contamination, and above all, prioritize patient safety.


Gain a comprehensive understanding of the essential elements involved in creating a safe and secure packaging component

Discover the pivotal role that manufacturing plays in guaranteeing the utmost quality and effectiveness of pharmaceutical packaging

Discover effective strategies for reducing risk through the implementation of quality-by-design principles and zero-defect methodology in product engineering


Head of Global Process Engineering
Datwyler

 joined Datwyler in 2017 and has held the positions of production manager, Datwyler Production System manager and Process & Validation manager in the Belgian plant before taking up the position of Head of Global Process Engineering. Before being part of the Datwyler organization, Tom worked for 14 years within an engineering & consultancy firm. He has a Masters in Industrial Engineering.

Webinar Date/Time: Tue, Sep 17, 2024 9:00 AM EDT

From Discovery to Delivery: Engineering Safe and Effective Pharmaceutical Packaging

Join industry experts in this webinar for valuable insights on selecting drug packaging systems with optimized functionality.

https://www.pharmtech.com/pt_w/flawless-functionality

When analyzing the functionality of injectable drugs, it is crucial to consider various factors, including the pharmaceutical packaging. It is essential to evaluate the desired field usage of the drug to ensure its safety and compatibility with the packaging. Additionally, optimizing patient comfort and compliance should be a priority, taking into account factors like the required injection volume, needle gauge, puncture frequency, and injection site. It is imperative to carefully assess and understand the functionality of the full packaging system together, and not just its individual pieces. Join us in this webinar as industry experts delve into the vital components of injectable drugs and share their valuable insights on creating a best-in-class drug packaging solution.

Discover the essential components of injectable drug functionality

Discover the various packaging components and their impact on the functionality of injectable drugs

Gain insight into how pharmaceutical packaging providers consider the functionality of drugs when creating innovative packaging solutions


Global Product Leader, Prefilled Syringes and Cartridges
Datwyler

 graduated as an industrial engineer in chemistry and started her career in the pharma industry. After 15 years of experience as a packaging development engineer and project manager, she moved to Datwyler. She joined Datwyler in 2007 and spent 7 years as a Technical Key Account Manager, providing technical support to customers, and 4 years as a Global Qualification and Validation Manager, working to set-up the Datwyler validation approach. She moved into the role of Global Platform Leader for Prefilled Syringes and Cartridges in 2018, making sure that the standard portfolio of the rubber components used for these packaging presentations secures Datwyler’s position as a market leader for PFS and cartridge sealing solutions.


Webinar Date/Time: Tue, July 25, 2024 10:00 AM EDT




Flawless Functionality: Optimizing Injectable Drug Stability and Performance

In the fast-paced world of pharmaceuticals, it is crucial for injectable drug developers to stay informed about the ever-changing requirements set forth by regulatory authorities. In this webinar, industry experts will educate the audience about the latest updates to USP and EU GMP requirements, and will explain how to confidently navigate the complexities of injectable drug regulations.

https://www.pharmtech.com/pt_w/regulatory-requirements

In the fast-paced world of pharmaceuticals, it is crucial for injectable drug developers to stay informed about the ever-changing requirements set forth by regulatory authorities. These updates not only ensure enhanced patient safety, but also help maintain strict adherence to standards when prescribing or administering injectable medications. In this webinar, industry experts will educate the audience about the latest updates to USP and EU GMP requirements, and will explain how to confidently navigate the complexities of injectable drug regulations.

Gain valuable insights into the latest regulatory updates, particularly the upcoming modifications to USP 382

Discover how pharmaceutical packaging suppliers are partnering with customers to provide comprehensive support in navigating the intricate regulatory environment surrounding injectable medications

Discover effective strategies to proactively anticipate and manage future regulatory changes, minimizing potential risks

, an experienced Manager of Regulatory Affairs at Datwyler since 2018, brings a wealth of knowledge and expertise to the pharmaceutical industry. With a Master's degree in Natural Sciences and 15 years of experience in Regulatory Affairs, Tabassam is well-versed in the intricacies of navigating drug regulations. In his current role, he holds global responsibility for submitting and updating Drug Master Files with health authorities, providing invaluable support to pharmaceutical companies seeking regulatory approvals. Additionally, Tabassam actively contributes to standardization efforts as a member of various esteemed groups, including the Ph. Eur. experts Group 16, ISO Technical Committee 76 / WG4, and the PDA Task Force on TR 73-2. His extensive involvement in these initiatives further showcases his commitment to staying at the forefront of regulatory advancements.


Webinar Date/Time: Tue, Jun 4, 2024 9:00 AM EDT




What's New and What to Do: Critical Updates to Regulatory Requirements for Injectable Packaging

Rubber components play a vital role in the packaging of pharmaceuticals. However, there has been growing concern about the presence of undesirable impurities like nitrosamines in rubber materials. This webinar aims to shed light on the significant advances made in the chemical cleanliness of rubber components over the past few decades.

https://www.pharmtech.com/pt_w/chemical-cleanliness

Rubber components play a vital role in the primary packaging of pharmaceuticals, offering excellent sealing capabilities. However, there has been growing concern about the presence of undesirable impurities like nitrosamines in rubber materials. This webinar aims to shed light on the significant advances made in the chemical cleanliness of rubber components over the past few decades. Industry experts will also provide insights into the extractables that can be expected from both older and more modern rubber formulations and will demonstrate how selecting the right compound and utilizing readily available extractables data can streamline the E&L (Extractables and Leachables) testing process.

Understand the advances of modern rubber formulations and the impact on pharmaceutical packaging

Gain insight into common challenges with extractables and leachables in pharmaceutical packaging and how to mitigate its occurrence

Recognize ways to use extractables data to streamline the E&L testing process

 studied Polymer Chemistry at the University of Leuven and received her MSc in 2013. She acquired a PhD for her dissertation on the controlled synthesis of conjugated polymers in 2017.
After gaining R&D experience at Kaneka Belgium, Tine started her career at Datwyler in 2018 as Manager of Material Development. In this role, she supports the development of new rubber formulations and raw material management, and helps customers with rubber compound-related questions, among other things. Additionally, she focuses on the field of Extractables & Leachables.



Webinar Date/Time: Thu, Apr 18, 2024 9:00 AM EDT




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