ISO 9001 is the International Standard that specifies requirements for a quality management system (QMS). Organizations use the standard to demonstrate the ability to consistently provide products and services that meet customer and regulatory requirements. It is the most popular standard in the ISO 9000 series and the only standard in the series to which organizations can certify.
At Framework, our team have the core knowledge and experience to do gap analysis audit and prepare you for certification audit by any recognised agency.
We make sure that ISO 9001 standard implementation does not just become a documentation activity but also a way of life for the organization that lays a foundation for Total Quality Management and quality conscious organizational culture.
By a thorough review of documents that includes records, files, procedures and other critical documentation of current processes, Our team can accurately scope the necessary effort involved to implement a process-focused quality management system solution that not only meets the requirements of ISO 9001 but is also customized to your Organizations working culture.
We offer onsite and online consultation solutions for ISO 9001 certification. Our customers have been utilizing our services not only for initial certification consultation but also for post certification consultation to ensure that we regularly add value to their business processes and quality standardization initiatives.
ISO 29001 defines the Quality management system requirements for the design, development, production, installation and service of products for the petroleum,
ISO 29001 standard is based on ISO 9001 and incorporates supplementary requirements emphasizing defect prevention and the reduction of variation and waste from service providers.
Our ISO 29001 certification consultancy involves mainly following steps :
Manufacturers of pressure equipment selling into most European countries (the European Economic Area) must make sure they comply with the requirements of the Pressure Equipment Directive.
The PED sets out essential requirements for pressure equipment and assemblies. They vary according to how much pressure, liquid, or gas the equipment is designed to contain. The PED does not tell manufacturers how to meet these requirements, allowing them the flexibility to meet the requirements with various manufacturing standards.
All equipment covered by the PED falls into one or more risk categories. After determining which category applies to your equipment, it has to comply with one or more conformity assessment modules which define the level of quality assurance and third-party involvement, including:
The PED provides three routes to conformity, depending both on the equipment and the choice of the manufacturer:
Third-parties must be registered Notified Bodies (NoBos), which are approved by an accreditation body.
The directive requirements can be met through the following methods: