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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
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
Understanding Quality Risk Management
Attendees will come away with the ability to recognize the purpose and value of Quality Risk Management QRM, explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions. In addition, they will be ...
- Basic & Intermediate
- 60 Mins
- Steven Laurenz
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
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
FDA Regulation of Artificial Intelligence - Machine Learning
AI/ ML will revolutionize medicine by making diagnosis and treatment more accessible and more effective. FDA has regulated medical device software by means of regulations and guidance for years, however, AI/ML programs fall outside the scope of these regulatio ...
- Basic & Intermediate
- 60 Mins
- Edwin Waldbusse
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
Recorded Webinar
Human Factors/ Usability Studies following ISO62366, the FDA Guidance, and the new FDA Draft Guidance
Human Factors/ Usability is the analysis of how people interact with medical devices. The process of conducting rigorous human factors studies throughout the design process, integrating it with the device risk analysis and design process, and validating the ef ...
- Basic & Advanced
- 60 Mins
- Edwin Waldbusse
Recorded Webinar
REACH and ROH Overview
REACH and RoHS conformity has banned problematic toxic and environmentally hazardous elements such as lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls (PBB), and polybrominated diphenyl ether (PBDE) in quantities not exceeding a maximum of ...
- Intermediate
- 90 Mins
- Kelly Thomas
Recorded Webinar
An Advanced Course on Lean Documents, Lean Configuration and Document Control
In this Lean Documents, Lean Configuration, and Document Control training learn the different types of lean documents and the usage of lean document principles; types of controlled documents; examples of lean and non-lean controlled documents. Pros and cons of ...
- Basic & Intermediate
- 90 Mins
- José Mora