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Category: Uncategorized

August 27, 2019August 27, 2019Uncategorized

ISO/IEC 20000-1 Transition

SERVICE MANAGEMENT Introduction The best way to distinguish your organization in the market is by providing high-quality services. Taking into […]

August 21, 2019August 21, 2019Uncategorized

ISO 9001:2015 Quality Management Systems – Requirements

Introduction Quality management is the act of managing all activities and functions needed to maintain a consistent level of excellence […]

March 27, 2019March 27, 2019Uncategorized

ISO 21500 Guidance on Project Management

ISO 21500 ISO 21500 provides guidance and high-level descriptions of concepts and processes that are considered important in project management […]

March 26, 2019March 26, 2019Uncategorized

ISO/IEC 17025:2017 – General Requirements for the Competence of Testing and Calibration Laboratories

Introduction The International Organization for Standardization (ISO) has released the most recent version of the ISO/IEC 17025 standard-the 2017 edition. […]

April 11, 2018April 11, 2018Uncategorized

General Data Protection Regulation (GDPR)

Introduction The European Union Directive 95/46/EC adopted in 1995 by the European Commission is an important component of the union wide privacy […]

April 11, 2018April 11, 2018Uncategorized

Six Sigma Green Belt

Six Sigma is a process improvement methodology that concentrates on one or more key areas, namely cost, schedule and quality. […]

April 11, 2018April 11, 2018Uncategorized

ISO 19600:2014 – Compliance Management Systems Guidelines

In the English dictionary, compliance is briefly described as the act or process of being in conformity with applicable regulations, […]

March 29, 2018September 23, 2021Uncategorized

When Intrusion Detection Systems & Vulnerability Management Solutions Fail

Network breaches happen.. from mega-corps, to governments to unsuspecting users, to well known security pros.. what isn’t excusable, is finding out  months or years later […]

March 25, 2018March 25, 2018Uncategorized

ISO 13485 Medical Devices Quality Management Systems Requirements for Regulatory Purposes

Introduction An audited and certified medical device quality management system issued by a third-party is often required, or strongly preferred, […]

March 25, 2018April 11, 2018Uncategorized

ISO 45001 Occupational Health and Safety Management System Requirements

Introduction The world that we live in has experienced rapid changes in technology, competition, economy, education and so on. It […]

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