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Any document, media piece, or email bearing your organization’s insignia or name must be absolutely error-free. Even a careless mistake in an email can damage a leader’s reputation and can make an entire company look bad. Proofreading is a skill anyone can lea ...
Unlock the potential of AI in finance with our transformative webinar, "ChatGPT for CPAs and Finance Professionals". In this 90-minute session, delve into how ChatGPT can be your partner in navigating complex financial landscapes, from automating routine accou ...
Effective technical writing is a cornerstone of successful FDA submissions, serving as a critical bridge between scientific data and regulatory review. Regulatory agencies like the FDA rely on clear, concise, and well-structured documentation to evaluate the s ...
CAPA stands for Corrective and Preventive Action. It's a systematic process used in industries like manufacturing, healthcare, and pharmaceuticals to identify, address, and prevent problems or non-conformities. CAPA is a crucial part of a quality management s ...
In this webinar, participants will explore advanced capabilities that take Excel automation and data analysis to the next level. We’ll begin by examining how Copilot can be used on multiple tables, allowing users to streamline complex data manipulation and ana ...
There are many shortcuts to do the work you do. This course shows many tips & tricks which many experts aren’t aware of and which save you lots of time. One of my favourite comments which came from this course was, “This Isn’t Excel, it’s Magic!” It also becam ...
Have you ever wanted to get paid for sharing your knowledge in a webinar but didn’t know where to start? What if you could present webinars without marketing yourself, finding attendees, or handling complex technology, yet still earn money? That’s exactly wha ...
It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement. This webinar will give you a comprehensiv ...
If you do any work that will be reported to the US Food and Drug Administration (FDA), Environmental Protection Agency (EPA), or Occupational Safety and Health Administration (OSHA), your work must be done under GLP. All methods must be validated, the proof t ...
How does it feel to be caught in the middle of a growing trade war -- rife with high import tariffs? These huge tariffs against China began in 2018. Having received comments from importers “benefiting” from these US tariffs, in August 2022, the USTR announced ...