ISO/IEC 27001:2013

ISO/IEC 27001:2013

This Certificate is Applicable to:

Business processes: Collecting, defining and managing requirements. Planning, designing, researching, developing, collaborating, implementing, manufacturing, documenting, verifying and quality assuring and hosting products. Submitting products for the American Food and Drug Administration (FDA) approval. Marketing, selling, consulting on, deploying and integrating products.

System/products: Clinical trials, medical devices, platforms, services, software and systems - either on-premises, mobile or in the Cloud (e.g. SaaS).

According to Statement of Applicability: Version 1.0, Date: February 4th 2018

ISO 27017:2015

ISO 27017:2015

This Certificate is Applicable to:

Collecting, defining and managing requirements. Planning, designing, researching, developing, collaborating, implementing, manufacturing, documenting, verifying and quality assuring and hosting products. Submitting products for the American Food and Drug Administration (FDA) approval. Marketing, selling, consulting on, deploying and integrating products.

ISO 27018:2014 Best Practices

ISO 27018:2014 Best Practices

This Certificate is Applicable to:

Collecting, defining and managing requirements. Planning, designing, researching, developing, collaborating, implementing, manufacturing, documenting, verifying and quality assuring and hosting products. Submitting products for the American Food and Drug Administration (FDA) approval. Marketing, selling, consulting on, deploying and integrating products.

ISO 27799:2016

ISO 27799:2016

This Certificate is Applicable to:

Collecting, defining and managing requirements. Planning, designing, researching, developing, collaborating, implementing, manufacturing, documenting, verifying and quality assuring and hosting products. Submitting products for the American Food and Drug Administration (FDA) approval. Marketing, selling, consulting on, deploying and integrating products.

ISO 22301:2012

ISO 22301:2012

This Certificate is Applicable to

Collecting, defining and managing requirements. Planning, designing, researching, developing, collaborating, implementing, manufacturing, documenting, verifying and quality assuring and hosting products. Submitting products for the American Food and Drug Administration (FDA) approval. Marketing, selling, consulting on, deploying and integrating products.