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Search Trainings
Recorded Webinar
Bad Standard Operating Procedures (SOPs) = Bad Training: Garbage In, Garbage Out
Standard Operating Procedures (SOPs) are the basis for a large part of the day-to-day training that most pharmaceutical employees are required to perform. Still, it is not widely understood how the writing of a procedure can have a positive or negative impact ...
- Basic & Intermediate
- 90 Mins
- Michael Esposit
On-Demand Webinar
How Accountants Can Use Chat GPT Effectively
ChatGPT has been created with one main objective - to predict the next word in a sentence, based on what's typically happened in the gigabytes of text data that it's been trained on. Once you give ChatGPT a question or prompt, it passes through the AI model a ...
- Basic & Advanced
- 60 Mins
- Justin Muscolin
On-Demand Webinar
Assertiveness Skills for Leaders, Managers and HR Professionals
Stop Feeling Silenced, Start Saying Yes (to Yourself)! Do you struggle to voice your ideas, feel constantly swamped, or like your priorities get sidelined? This energizing workshop is your key to unlocking assertive leadership. Learn how to speak clearly, set ...
- Basic & Intermediate
- 60 Mins
- Suzanne Blake,
Recorded Webinar
Basic Issues of Method Validation Compliance under Good Laboratory Practices
Any laboratory that supports products for sale or use in the United States must follow Good Laboratory Practices (GLP), a comprehensive system that guarantees the validity of results. If you work in pharmaceuticals, chemicals, petrochemicals, and environmental ...
- Basic & Intermediate
- 60 Mins
- John Fetzer
On-Demand Webinar
Excel ChatGPT PivotTables Advanced Data Management Functions & Much More
Gain easy-to-understand and practical “hands-on” knowledge of ChatGPT and Artificial Intelligence (AI) at an intermediate level with a focus on significantly enhancing capabilities in Microsoft Excel. Harness the awesome power of AI to take Excel to a new lev ...
- Intermediate
- 90 Mins
- Ray Evans
Recorded Webinar
Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device
Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal between the test method and the product or process it is designed to detect. For example, while a defect-free process is desirable, a test ...
- Intermediate
- 90 Mins
- José Mora
Recorded Webinar
European Union Device Regulation (EU MDR)
The EU MDR replaces the MDD and expands the requirements for conformance. The MDR contains 174 pages with 123 "Articles" in 10 "Chapters" and 17 "Annexes". In contrast the MDD has 60 pages. New requirements are added and existing requirements are expanded. The ...
- Intermediate
- 60 Mins
- Edwin Waldbusse
Recorded Webinar
Risk-based Design Control - The New Paradigm for Medical Device Design
Risk management overarches projects associated with a particular product family, given that risks will both remain and change as new design features and medical indications for use evolve with a particular device. Design control is not only a requirement of t ...
- Intermediate
- 60 Mins
- José Mora
On-Demand Webinar
ChatGPT for Excel
This course is designed to teach learners how to use CHATGPT for Excel, a powerful tool that can help you automate tasks, analyze data, and create reports in Excel. Throughout the course, learners will explore the features and capabilities of CHATGPT for Excel ...
- Basic
- 60 Mins
- Tom Fragale
Recorded Webinar
Chat GPT's Bold Innovation: Reshaping HR Learning & Development
"ChatGPT's Bold Innovation: Reshaping HR Learning & Development" is an insightful exploration into the transformative role of AI in human resources. This topic delves into how ChatGPT, a state-of-the-art AI language model, is redefining the boundaries of learn ...
- Basic & Advanced
- 60 Mins
- Thea Ducrow PHD