Attorneys Mauricio Uribe and Dan Altman present a Webinar focusing on strategic considerations for patent prosecution in the United States in view of the statutory requirements of Section 101.
Attorneys Mauricio Uribe, Dan Altman and Of Counsel Hironori Kubota hosted a detailed Webinar focusing on strategic considerations for patent prosecution in the United States in view of the statutory requirements of Section 101.
Attorneys Sabing Lee and Christy Lea presented a detailed webinar focusing on strategic considerations for medical device patents in Europe and the U.S.
Attorneys Maria Anderson, Jeremy Carney, Bryan McWhorter, Alex Martinez, Mauricio Uribe hosted a webinar on Strategic Considerations in Patent Subject Matter Eligibility Under Revised USPTO Guidance
GMP Sub Part - "H" provide valuable information regarding holding and control of pharmaceutical goods, while Sub Part - "I" shows laboratory control and Sub Part - "J" give ideas about record and reports. Very helpful to pharma professionals.
Attorneys Mauricio Uribe, Dan Altman and Of Counsel Hironori Kubota hosted a detailed Webinar focusing on strategic considerations for patent prosecution in the United States in view of the statutory requirements of Section 101.
Attorneys Sabing Lee and Christy Lea presented a detailed webinar focusing on strategic considerations for medical device patents in Europe and the U.S.
Attorneys Maria Anderson, Jeremy Carney, Bryan McWhorter, Alex Martinez, Mauricio Uribe hosted a webinar on Strategic Considerations in Patent Subject Matter Eligibility Under Revised USPTO Guidance
GMP Sub Part - "H" provide valuable information regarding holding and control of pharmaceutical goods, while Sub Part - "I" shows laboratory control and Sub Part - "J" give ideas about record and reports. Very helpful to pharma professionals.
Validation is the process of checking of the process, equipment and method whereas qualification is solely done for equipment and qualification of instrument helps in quality of pharmaceutical product.
Supplement 6- Annex9- WHO guideline: Temperature and humidity monitoring systems
Technical supplement to WHO Technical Report Series, No. 961, 2011 Annex 9: Model guidance for the storage and transport of time and temperature–sensitive pharmaceutical products
Types of validation & validation of specific dosage.pptxankitanakashe21
Validation is a proven assurance of the process efficiency and sturdiness, and it is the full-fledged quality control tool for the pharmaceutical industries. It eliminates the chances of batch failures as the products are manufactured as per pre optimization of each manufacturing steps. The conventional process of testing at last stage created much problems in maintaining the uniformity of each batch but with the introduction of concept of validation, it has been easy to maintain the batch uniformity of the product along with imparting quality in them.
GMP Sub Part - "E" gives valuable information regarding Control of components and Product containers and closures during pharmaceutical manufacturing while Sub Part - "F" gives ideas about pharmaceutical production and process control. Very helpful to pharma professionals.
Supplement 8- Annex9- WHO guideline: Temperature mapping of storage areas
Technical supplement to WHO Technical Report Series, No. 961, 2011 Annex 9: Model guidance for the storage and transport of time and temperature–sensitive pharmaceutical products
Validation of lab instruments and quantitative test methods Mostafa Mahmoud
This lecture shows the procedures applied when going to validate your laboratory instruments and quantitative test methods also either FDA approved or laboratory developed tests.
Partner Ben Anger discusses the latest developments and advanced strategies for PTAB practice, specifically focused on the petitioner side. Ben covers issues related to selecting the prior art, anticipation versus single-reference obviousness, motivation to combine, post-institution practice, and more.
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Validation is the process of checking of the process, equipment and method whereas qualification is solely done for equipment and qualification of instrument helps in quality of pharmaceutical product.
Supplement 6- Annex9- WHO guideline: Temperature and humidity monitoring systems
Technical supplement to WHO Technical Report Series, No. 961, 2011 Annex 9: Model guidance for the storage and transport of time and temperature–sensitive pharmaceutical products
Types of validation & validation of specific dosage.pptxankitanakashe21
Validation is a proven assurance of the process efficiency and sturdiness, and it is the full-fledged quality control tool for the pharmaceutical industries. It eliminates the chances of batch failures as the products are manufactured as per pre optimization of each manufacturing steps. The conventional process of testing at last stage created much problems in maintaining the uniformity of each batch but with the introduction of concept of validation, it has been easy to maintain the batch uniformity of the product along with imparting quality in them.
GMP Sub Part - "E" gives valuable information regarding Control of components and Product containers and closures during pharmaceutical manufacturing while Sub Part - "F" gives ideas about pharmaceutical production and process control. Very helpful to pharma professionals.
Supplement 8- Annex9- WHO guideline: Temperature mapping of storage areas
Technical supplement to WHO Technical Report Series, No. 961, 2011 Annex 9: Model guidance for the storage and transport of time and temperature–sensitive pharmaceutical products
Validation of lab instruments and quantitative test methods Mostafa Mahmoud
This lecture shows the procedures applied when going to validate your laboratory instruments and quantitative test methods also either FDA approved or laboratory developed tests.
Partner Ben Anger discusses the latest developments and advanced strategies for PTAB practice, specifically focused on the petitioner side. Ben covers issues related to selecting the prior art, anticipation versus single-reference obviousness, motivation to combine, post-institution practice, and more.
Partners Susan Natland and Jessica Sganga discussed potential trademark and copyright issues in the emerging metaverse, including the surge in popularity of NFTs (non-fungible tokens) and how they may affect intellectual property protections. Get up-to-speed on the “hot” cases in this evolving area and get practical tips on how best to protect your intellectual property from infringement in this virtual space.
Speakers: Susan Natland, Jessica Sganga
Knobbe partners Jeff Van Hoosear (OC) Jason Jardine (SD) and associate Julia Hanson (SD) recently gave a presentation at San Diego Fashion week on intellectual property for designers and artists. The presentation explored what IP is, why it is important to designers, top 5 misconceptions, how to get a copyright, how to get a trademark and how to get a design patent.
Partner Mauricio Uribe continued the two-part, comprehensive discussion on responding to IP threats and assertions. The presentation focused on a more detailed exploration of the topic and strategic implications for various scenarios.
Speakers: Mauricio Uribe
Partners Melanie Seelig and Mauricio Uribe kicked off a two-part, comprehensive discussion on responding to IP threats and assertions. The presentation served as an introduction to the topic and provided more general information.
Speakers: Melanie Seelig and Mauricio Uribe
Partner Mauricio Uribe continued the two-part, comprehensive discussion on open-source software and third-party vendors. The presentation focused on a more detailed exploration of the topic and strategic implications for various scenarios.
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Partner Jason Gersting, Ph.D. moderated a panel of his peers in a discussion about learning how to identify the waves in current written description and enablement law and tips for smoothly riding them to expand, enhance and protect life sciences intellectual property rights. Panelists included Knobbe Martens partners Jessica Achtsam, Eric Furman, Ph.D., and Dan Altman.
Partner Mauricio Uribe kicked off a two-part, comprehensive discussion on open-source software and third-party vendors. The presentation served as an introduction to the topic and provided more general information.
Speakers: Mauricio Uribe
Partner Mauricio Uribe continued the two-part, comprehensive discussion on data privacy. The presentation focused on a more detailed exploration of the topic and strategic implications for various scenarios .
Speakers: Mauricio Uribe
Partner Mauricio Uribe kicked off a two-part, comprehensive discussion on data privacy. The presentation served as an introduction to the topic and provided more general information.
Speakers: Mauricio Uribe
Partners Mauricio Uribe and Vlad Lozan gave an informative presentation on design patent law in the United States. The partners provided best practices for filing and prosecuting design patents in the U.S. and techniques and strategies for including multiple design embodiments in design patent applications. They also discussed how to identify and protect visual elements in computer-related technologies and how to integrate design patents into a holistic intellectual property strategy.
Speakers: Mauricio Uribe, Vlad Lozan
Partners Melanie Seelig and Mauricio Uribe continued the two-part, comprehensive discussion on trade secrets. The presentation focused on a more detailed exploration of the topic and strategic implications for various scenarios .
Speakers: Melanie Seelig and Mauricio Uribe
Partners Melanie Seelig and Mauricio Uribe kicked off a two-part, comprehensive discussion on trade secrets. The presentation served as an introduction to the topic and provided more general information.
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Partners Mauricio Uribe and Paul Stellman continued the two-part, comprehensive discussion of strategic planning for capturing and protecting intellectual property. The presentation focused on a more detailed exploration of the topic, diving into the best intellectual property portfolios and cost deferrable strategies to maximize intellectual property spend.
Speakers: Mauricio Uribe and Paul Stellmann
Partners Mauricio Uribe and Vlad Teplitskiy gave an informative presentation on strategic considerations for claim drafting electrical and telecommunications Inventions. The partners provided illustrative claim drafting examples and best practices for defining claim scope, as well as claim drafting strategies for avoiding or minimizing unintentional functional claiming.
Speakers: Mauricio Uribe, Vlad Teplitskiy
Partners Maria Stout and Paul Stellman kicked off a two-part, comprehensive discussion of strategic planning for capturing and protecting intellectual property. The presentation served as an introduction to the topic and provided more general information.
Speakers: Maria Stout and Paul Stellmann
Partners Melanie Seelig and Mauricio Uribe continued the two-part, comprehensive discussion of strategic considerations regarding employment and vendor agreements. The presentation focused on a more detailed exploration of managing employment and vendor agreements, follow-on agreements, and sample language and practical examples.
Speakers: Melanie Seelig and Mauricio Uribe
Partners Melanie Seelig and Maria Stout kicked off a two-part, comprehensive discussion of strategic intellectual property considerations regarding employment and vendor agreements. This presentation served as an introduction to the topic and provided more general information.
Speakers: Melanie Seelig and Maria Stout
Knobbe Practice Japan Webinar Series
Partner Mauricio Uribe provided a detailed discussion focused on advanced patent claim drafting techniques for artificial intelligence technologies and related applications. The discussion covered: claim drafting techniques to capture different aspects of artificial intelligence/machine learning technologies; considerations for detecting infringement and possible alternative trade secret protection in the United States; and considerations for patent subject matter eligibility under Section 101.
This was the second and more advanced part of the webinar on understanding and protecting artificial intelligence and machine learning technologies. If you missed the introductory webinar on this topic, you can view the recording here.
Speakers: Mauricio Uribe and Kenny Masaki
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