Standards can be implemented and adopted for internal benefit only, without the requirement for ISO certification or ISO registration.
CRMs must be characterized using analytical methods validated according to ISO/IEC 17025 (http://www.iso.org/iso/home.html) during development and production to fulfil the requirements of ISO Guide 34 (http://www.iso.org/iso/home.html).html
EQA and other methods of interlaboratory comparison are a formal requirement of ISO 15189, but are rarely required by legislation.
Validation is a formal requirement of ISO 15189 (section 5.5.2): 'The methods and procedures selected for use shall be evaluated and found to give satisfactory results before being used for medical examinations'.
Security risk analysis is a basic requirement of ISO 27002 [ 15], internationally recognised as the generic information security standard.
For safety reasons an upper temperature limit is included in the requirements for refillable hydrogen tanks (ISO 15869) which sets the limit for any fill optimization.
All analyses are in compliance with the requirements for quality and competence (ISO 15189 2012) for medical laboratories.> Plasma aminoacid concentrations will be measured by ion-exchange chromatography (IEC) with ninhydrin detection.
The Scientific Working Group on Digital Evidence (SWGDE) produced a 2002 paper, "Best practices for Computer Forensics", this was followed, in 2005, by the publication of an ISO standard (ISO 17025, General requirements for the competence of testing and calibration laboratories).
The accompanying ISO 16919 standard: Requirements for bodies providing audit and certification of candidate trustworthy digital repositories, has been published very recently and now the ISO organization needs to be set up in the different countries, including the training of national auditors.
The requirements for a reference material producer under ISO Guide 34 accreditation cover additional data such as homogeneity of the material and short-term and long-term stability [ 19].
