Accreditations
The team at TAC Portal boast a significant collection of accreditations from some of the world's leading digital standards.
ISO-13485 Medical Devices QMS
ISO 13485 ensures that medical devices and software are safe for their purpose by meeting internationally recognised standards.
ISO-9001 Quality Management
ISO 9001 is the international standard for quality management systems. This standard ensures that certified companies offer services and products that meet regulatory and customer requirements.
ISO-27001 Information Security
ISO 27001 is an international information security framework outlining the specifications for implementing an information security management system.
ISO-14001 Environmental Management
The ISO 14001 framework is the international standard specifying requirements for an effective environmental management system to enhance our environmental performance.
Cyber Essentials Plus
The Cyber Essentials Plus certification proves that the security measures a company has taken are operational after undergoing an independent audit and ensure they conform to government standards in cyber security.
CREST Penetration Testing
CREST is an internationally recognised certification and accreditation body, representing and supporting the technical information security market.
Compliance
The TAC Portal complies to the following standards and frameworks.
UL 2900-1 Data Security
The Data Security UL 2900-1 standard (run under the U.S. Food & Drug Administration) ensures that products demonstrate effective implementation of security controls. This standard ensures that any vulnerabilities to cyber-attack have been appropriately risk assessed, addressed and subjected to an appropriate level of testing.
ISO-14971 Risk Management
ISO 14971 outlines the international requirements of risk management systems for medical devices. Defining the best practices of a medical device's lifecycle. It is a core consideration with ISO 13485.
IEC-62304 Software Lifecycle
IEC 62304 is an internationally recognised standard for medical device software defining a framework that is agreed for processes occurring during the product lifecycle.