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Webinars
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Trademark Modernization Act (TMA): From Principle to Practice
An extensive examination of the Trademark Modernization Act (TMA) and its useful ramifications for registering, preserving, and safeguarding trademarks in the United States is offered in this webinar. Discover the main changes, including the revised expungement and reexamination processes, the shortened response deadlines, and audit prevention advice.
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Discover Hot Trademark Topics Around the World
Hear from eminent trademark specialists as they discuss the most recent developments and difficulties associated with registering trademarks in China, the United States, and Europe, among other important worldwide regions. Learn important information about new regulations, regional trademark practices, and international brand protection tactics.
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Brazilian Innovation Law: Break the Fortress of the Roman Empire Influence
Learn about international technology transfer procedures and the difficulties that colleges encounter when trying to make their research profitable. Discover from professionals the creative approaches and IP protection devices that universities worldwide employ to make their research and development marketable.
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Business In Canada: Ensuring Language is not a Barrier
Learn how to overcome language barriers in the Canadian market to make sure your company succeeds in a multilingual setting. With an emphasis on localization and translation, this webinar will address essential communication techniques that are suited to Canada's distinct language environment.
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How to Secure the Perfect Partner when Procuring Language Services
Discover how to locate and hire the ideal language service provider for your requirements. This webinar will walk you through key factors, such as financial stability and technical proficiency, to help you make the best decision for your language service purchase that will pay off in the long run.
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Utilizing Brazil´s New IP System for Pharma and Academics to Optimize Innovation
Explore how the IP landscape in Brazil is changing and how this affects academia and the pharmaceutical business in our webinar. Learn about fresh prospects for technology transfer, market access, and patent protection brought about by recent legislation. Universities, research facilities, and pharmaceutical businesses looking to increase their capacity for innovation in this fast-growing market should not miss this event.
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Unlocking IP Potential in Brazil: Navigating New BRPTO Reforms for Global Success
Brazil plays a vital role in international intellectual property policies; the webinar highlighted recent improvements to the BRPTO. The advantages of the Patent Prosecution Highway (PPH) agreements, Brazil's ratification of the Madrid Protocol, and the accelerated patent examination procedure were among the main subjects discussed. Experts from SHIP Global IP and Venturini IP talked about how these changes can open up new avenues for IP protection in Brazil.
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Making the Most of your Medical Interpreters
This covers planning, discussions, and debriefing, concentrated on finding solutions to typical problems in healthcare interpreting. It included advice on how to use interpreters effectively, emphasized the advantages of remote interpreting, covered legal requirements, and discussed communication techniques with patients who do not speak English. Additionally, the workshop included recommendations for raising patient happiness and results in a range of healthcare environments.
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Entering the Chinese Market: Essential Steps for Medical Device Registration and Compliance
The practical and legal difficulties of breaking into the Chinese market. Recent developments in clinical trials, regulatory framework, classification, device registration, and the NMPA Legal Agent were among the important subjects covered. There was also discussion of best practices and linguistic issues for compliance, with SeproTec and Cisema experts offering advice on navigating the Chinese medical device market.
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How ISO 13485 and the EU MDR will Affect your Business from a Translation Point of View
The effects of the EU MDR and ISO 13485 on the medical device sector were the main topics of discussion throughout the webinar. The significance of uniform standards, the function of ISO 13485 in regulatory compliance, and the CE marking procedure were among the main subjects covered. SGS and SeproTec experts talked on quality management systems, legal requirements, and real-world implementation obstacles. They also provided advice on how to remain compliant with changing rules.
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