Blog2022-01-15T20:42:38+00:00

AssurX Blog

Straight talk for regulated industries.

2305, 2017

Strong Document Control Critical For NERC Compliance

May 23rd, 2017|Archives, Energy & Utilities Industry, NERC Compliance, Regulatory Compliance Management|

Document control is invaluable to utilities trying to prevent or learn from system outages. Stakes are high. Consider the cost of outdated or insufficient documentation in terms of leg [...]

1605, 2017

How Will Real-World Evidence Impact 2017 FDA Guidances?

May 16th, 2017|Archives, FDA Regulated Industries, Medical Device Industry, Quality Management, Regulatory Compliance Management|

The Advanced Medical Technology Association (AdvaMed) wants the Food and Drug Administration (FDA) to understand that medical device manufacturers want clarity on FDA's heightened focu [...]

805, 2017

CDRH Report: Quality Management Insights For Medical Device Manufacturers

May 8th, 2017|Archives, FDA Regulated Industries, Medical Device Industry, Quality Management|

FDA's Center for Devices and Radiological Health (CDRH) provided a glowing self-assessment in a recent report. The CDRH met its 2016 strategic objectives for several initiatives pertai [...]

305, 2017

Cloud Computing Impact in the Energy and Utilities Sector

May 3rd, 2017|Archives, Energy & Utilities Industry, NERC Compliance, Regulatory Compliance Management|

Technology-averse energy & utilities companies are about to embrace the power of cloud computing technology, say many leading experts. Cloud Computing Technology = Enhanced Perform [...]

1704, 2017

Prioritize QMS Process Automation or Risk Failure

April 17th, 2017|Archives, eMDR, FDA Regulated Industries, Food & Beverage Industry, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management|

A common pitfall in QMS process automation occurs with a poorly planned process automation strategy.  Too often, the temptation is to automate all quality processes at once and streaml [...]

1104, 2017

Successful QMS Implementation Requires Clearly Defined Processes

April 11th, 2017|Archives, eMDR, FDA Regulated Industries, Food & Beverage Industry, Medical Device Industry, Pharmaceutical Industry, Quality Management, Regulatory Compliance Management|

Industry-leading quality management systems (QMS) are built with clearly defined processes and workflows developed by the implementation team. While initially it may seem overwhelming, [...]

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