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The ISO 27701:2019 and GDPR documentation kit is a comprehensive set of editable MS Word files that cover all aspects of the Privacy Information Management System and the General Data Protection Regulation. It includes a sample ISO ISO 27701 manual, 23 PIMS and GDPR policies, 12 ISO 27001 and GDPR procedures, 9 standard operating procedures, and six process ...

The EQMS Documentation Kit for QMS 9001:2015 and EMS 14001:2015 includes 220 editable MS Word files, a QMS EMS Manual, 11 procedures, standard operating procedures, process flow charts, exhibits, sample forms, and an environment management plan. The kit also includes an audit checklist with over 700 questions, including QMS 9001 and EMS 14001 requirements an...

The CE Mark Documentation Kit for Steel Structure is a set of 70 editable MS Word files that address all elements of CE Mark for steel structure certification. It includes a manual, mandatory procedures, QMS procedures, exhibits, readymade formats, standard operating procedures, and job descriptions and specifications. The kit includes a manual defining DIN ...

The Social Compliance Documentation Kit for Social Accountability is a set of 140 editable MS Word files that address all elements of Ethical Best practices according to various international standards. The kit includes 13 mandatory procedures, 35 standard operating procedures, 11 sample policies, 05 social committee documents, 04 exhibits, 07 aspects/ohm ha...

The ISO IFS Food version 8 Documents are a set of 200 editable MS Word files that cover all requirements for food processing organizations. The kit includes IFS food documents such as the IFS food safety manual, mandatory procedures, blank formats/templates, standard operating procedures, exhibits, process approaches, HACCP documents, food safety culture, au...

The ISO 28000 Documentation and Training Kit is a comprehensive resource for establishing and implementing a security management system (SMS) to ISO 28000:2022 requirements. The kit includes over 100 editable files and training presentation PPTs, including manuals, procedures, SOPs, policies, audit checklists, and blank formats. The ISO 28000 manual, audit c...

This ISO 17025 internal auditor training online course is specifically designed for those who want to learn auditing techniques based on ISO 17025:2017 as well as to know ISO 17025:2017 requirements in detail. The ISO 17025 auditor training online course helps laboratory employees to qualify as 'Internal Auditors' for Laboratory Management System based on IS...

This ISO/IEC 17025 lead auditor training course, which comprises lectures, handouts, videos, an audit checklist, and exams, is designed to provide training and certification to become an ISO/IEC 17025 lead auditor for laboratory management systems. This ISO/IEC17025 lead auditor training is an online course; you will learn everything you need to know as the ...

The ISO/IEC 17029:2019 auditor training kit includes over 180 editable PPT slides, a user manual, case studies, and audit checklists in English. It covers six modules: overview, requirements, documented information, internal audit of the management system, internal audit records, and accreditation steps. The kit also includes a trainer's guide, handouts, wor...

The ISO 37301:2021 auditor training kit is a comprehensive resource for organizations aiming to improve their compliance management system. The kit includes 195 editable PPT slides, over 100 pages of handouts, audit checklists, audit forms, case studies, a trainer's guide, workshops, case studies, and an internal auditor training certificate. The training co...

ISO 13485:2016 auditor training contains more than 200 editable PPT slides and 125 pages of user manual, audit forms, case studies, and ISO 13485 audit checklists, which will be delivered in editable format. The total content of the ISO 13485 PowerPoint kit is editable and given in MS Word and PowerPoint presentations. To know more, visit here: https://www.g...

ISO 13485 2016 documents contain more than 100 editable MS Word files. These editable documents address all the elements of the medical device quality management system. Global Manager Group has designed a ready-to-use ISO 13485 2016 documents kit to comply with Medical Devices manufacturing QMS. Our ISO 13485 documents include the ISO 13485 Quality Manual, ...