Ready for ESG NextGen, or still submitting like it’s 2015? 网络研讨会点播 Ready for ESG NextGen, or still submitting like it’s 2015? Learn how to prepare for ESG NextGen with automated, compliant submission workflows. Watch the webinar…Certara2026 年 2 月 5 日
Certara and ANVISA Partner to Launch eCTD 4.0 Submissions of Drug Applications in Brazil Through GlobalSubmit™ software Announcement Certara and ANVISA Partner to Launch eCTD 4.0 Submissions of Drug Applications in Brazil Through GlobalSubmit™ software Certara and ANVISA have joined forces to enable eCTD 4.0 submissions in Brazil using GlobalSubmit™…Certara2025 年 11 月 13 日
Differences between eCTD 4.0 and eCTD 3.2.2 Submissions – What You Need to Know On-Demand Webinar Differences between eCTD 4.0 and eCTD 3.2.2 Submissions – What You Need to Know Access our on-demand webinar to explore the key differences between eCTD 4.0 and eCTD 3.2.2.…Certara2025 年 8 月 11 日
Regulatory Operations Best Practices for Health Canada Submissions Blog Regulatory Operations Best Practices for Health Canada Submissions Health Canada submissions now require eCTD/CESG; regulatory operations expert support can streamline the process and…Certara2025 年 8 月 11 日
FDA ESG NextGen for Regulatory Submissions Blog FDA ESG NextGen 助力监管申报 The FDA ESG NextGen for Regulatory Submissions has replaced the FDA’s WebTrader and simplifies pharmaceutical…Certara2025 年 6 月 25 日
eCTD 4.0: When & Where it will be Implemented Next On-Demand Webinar eCTD 4.0:When & Where it will be Implemented Next Associate Director, Regulatory Operations Over 20 years of experience in eCTD submissions and FDA interactions.…Certara2025 年 4 月 11 日
GlobalSubmit eCTD 4.0 Webinars On-Demand Webinar GlobalSubmit eCTD 4.0 Webinars The world of electronic regulatory submissions is about to change with the introduction of eCTD…Certara2024 年 12 月 3 日
Best Practices for a Successful eCTD Submission Blog 成功递交 eCTD 的最佳做法 Learn common pitfalls that pharmaceutical sponsors encounter during the regulatory eCTD submission procedure and best…Certara2024 年 3 月 5 日
Answers to Drug Developers’ Frequent Electronic Common Technical Document Questions Blog 药物开发人员常见电子通用技术文件问题解答 Although the Electronic Common Technical Document (eCTD) has been around for many years, it continues…Certara2023 年 12 月 12 日
10 Things to Know About eCTD 4.0: Embracing the Future Regulatory Submissions Blog 10 个关于 eCTD 4.0 的须知事项:迎接未来的监管提交 In this blog post, we explore the top 10 things you need to know about…Certara2023 年 10 月 17 日