Pharmaceutical manufacturing sites continuously compete, even within the same company to maintain production volumes and...
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikel...
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikel...
Skills-based hiring has been a topic of interest for many businesses and governments for the past few years. But even as...
This webinar describe, As part of the Case for Quality program US FDA noted how an excessive focus by the industry on co...
This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for compliant human factors/usab...
Pharmaceutical and other FDA-regulated industries are tasked with safely manufacturing products for people (or animals)...
Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal b...
This live interactive presentation will also discuss the regulations associated with the detection, correction, and prev...
FDA has substantial authority to oversee regulated companies and their operations. The primary purpose of FDA is to assu...
Internal audits are not just an important requirement for effective corporate governance – they are intended to sh...
FDA and the EU have tried to harmonize device regulatory requirements for over 25 years. Major differences between the F...
Internal Audit should be a key part of self-awareness and understanding strengths and weaknesses within your Quality Man...
Save time and money with these effective prescreening tips and tricks from an active recruiter.
“The future belongs to individuals and companies who embrace the entrepreneurial spirit, whether that is inside or...
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