{"id":8057,"date":"2022-06-28T09:18:44","date_gmt":"2022-06-28T09:18:44","guid":{"rendered":"https:\/\/www.aqscert.org\/training-on-international-standards\/"},"modified":"2023-08-08T21:31:29","modified_gmt":"2023-08-08T21:31:29","slug":"training-on-international-standards","status":"publish","type":"page","link":"https:\/\/www.aqscert.org\/en\/training-on-international-standards\/","title":{"rendered":"Training on international standards"},"content":{"rendered":"

[vc_row][vc_column][vc_tta_tour color=”peacoc”][vc_tta_section title=”Audience 9001″ tab_id=”1656407067860-ba7f1882-cd56″][vc_column_text]AUDITOR \/CHIEF AUDITOR OF THE MANAGEMENT SYSTEM: AUDIT METHODOLOGY<\/span><\/p>\n\n\n\n\n\n\n\n\n\n\n
AUDITOR \/CHIEF AUDITOR OF THE MANAGEMENT SYSTEM: AUDIT METHODOLOGY<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 2 days (16 hours)<\/span><\/td>\n<\/tr>\n
Updated course for new standard<\/strong><\/span><\/td>\n<\/tr>\n
The implementation of the auditor\/Chief Auditor Management System training is conducted in a modular and provides for the payment of a first incoming module, dedicated to audit methodology, followed by various training modules for third party auditors. The input module (16 hours) in the audit methodology, in accordance with UNI EN ISO 19011:2012 of ISO\/IEC 17021-1:2015, is valuable for access to third-party training courses per auditor (24 hours) for various full management systems, hence the third part training course for 40 hours total, has anticipated duration and recognition of the certification bodies of personnel for the subsequent registration of the Auditor \/Chief Auditor of the Management System<\/span><\/td>\n<\/tr>\n
OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
The course has the following objectives: <\/span><\/p>\n

\u00b7 Clearly adopt UNI EN ISO 19011:2012 and ISO\/IEC 17021-1:2015 in order to conduct internal audit\/external management systems.<\/span><\/p>\n

\u00b7 To develop methodologies for proper and effective conduct of audits<\/span><\/p>\n

\u00b7 Develop the necessary personal and professional skills of the auditor to effectively carry out their work<\/span><\/p>\n

\u00b7 Provide practical assistance to improve the communication process during the audit.<\/span><\/td>\n<\/tr>\n

CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
The course is theoretical and practical type, with good audit practices to aim at learning as efficiently as possible of audit management system.<\/span>
\nThe main arguments to be addressed: \u2013 UNI EN ISO 19011:2012 e ISO\/IEC 17021-1:2015\u00b7 ISO\/IEC 17021-1:2015 references to ISO\/IEC TS 17021 of part 2, 3, 4, 5, 6, 7\u00b7 \u2013 Audits of the first, second and third parts \u2013 Characteristics and benefits of audits \u2013 Topics and definitions of auditing <\/span>\u00b7 \u2013 Principles of auditing<\/span><\/p>\n

\u00b7 \u2013 PDCA applied to the audit process<\/span><\/p>\n

\u00b7 – Managing an audit program<\/span><\/p>\n

\u00b7 \u2013 Conducting an audit<\/span><\/p>\n

\u00b7 Effective communication during the audit<\/span><\/p>\n

\u00b7 \u2013 Nonconformities<\/span><\/p>\n

\u00b7 Analysis of the primary cause and corrective actions<\/span><\/p>\n

\u00b7 Competence and evaluation of auditors<\/span><\/p>\n

\u00b7 Registers of professional auditors<\/span><\/p>\n

\u00b7 A code of courtesy.<\/span><\/p>\n

The course includes teamwork s\u00e9ance and exercise. The work that will be analyzed in the classroom will give a valid result (continuous assessment) for admission to the written exam to be held at the end of the course.<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Auditor 14001″ tab_id=”1656408125281-f4ed0b1e-064f”][vc_column_text]AUDITOR \/LEAD AUDITOR OF ENVIRONMENTAL MANAGEMENT SYSTEMS ISO 14001<\/span><\/p>\n\n\n\n\n\n\n\n\n\n
AUDITOR \/LEAD AUDITOR OF ENVIRONMENTAL MANAGEMENT SYSTEMS (ACCREDITED BY RICEC)<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 24 hours in 3 days \u2013 \u20ac900,00 (+ T.V.SH if needed)<\/strong><\/span><\/td>\n<\/tr>\n
Updated course for new standard<\/strong><\/span><\/td>\n<\/tr>\n
OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
The course aims to provide knowledge and tools to enable programming, planning, execution, reporting and management requirements of independent auditing of an Environmental Management System in accordance with INI EN ISO 14001:2015, presenting theoretical and practical study (exercise application and group discussions) referring to the component elements of an Environmental Management System taking into account the new 2015 edition. <\/span><\/p>\n

The objectives for this course are:<\/span><\/p>\n

\u00b7 Training participants with the necessary knowledge to assess whether an Environmental Management System has been applied effectively in accordance with UNI CEI EN ISO IEC 17021:2015;<\/span><\/p>\n

\u00b7 Fully understand the meaning of the terminology used (environmental aspects, legal and regulatory requirements, risk, contexts, etc.)<\/span><\/p>\n

\u00b7 Accurate interpretation of the requirements of THE UNII EN ISO 14001:2015 in the context of the audit of the third part.<\/span><\/p>\n

\u00b7 Planning methodology and implementation of appropriate and effective audits of the Environmental Management System<\/span><\/p>\n

\u00b7 Methods taken to require audit evidence necessary to assess the degree of compliance of environmental management system EN ISO 14001:2015<\/span><\/p>\n

\u00b7 Communicate effectively during interviews and written audit accounts<\/span><\/td>\n<\/tr>\n

CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
The main topics that are discussed in the following: <\/span><\/p>\n

\u00b7 Generally<\/span><\/p>\n

o Applicable legislation on auditing SMM<\/span><\/p>\n

o IAF sectors for accreditation and for environmental certification<\/span><\/p>\n

o Environmental Management<\/span><\/p>\n

\u00b7 SMM for auditor\/chief auditor<\/span><\/p>\n

o Reference context and stakeholders<\/span><\/p>\n

o Environmental Aspects<\/span><\/p>\n

o Mandatory requirements<\/span><\/p>\n

o Requirements of UNI EN STANDARD ISO 14001:2015<\/span><\/p>\n

\u00b7 Independent audit process: ISO IEC 17021-1:2015, ISO\/IEC TS 17021-2:2015<\/span><\/p>\n

\u00b7 PDCA and the audit process<\/span><\/p>\n

\u00b7 Preparation of audit<\/span><\/p>\n

\u00b7 Audit activity<\/span><\/p>\n

\u00b7 Follow-up Activity<\/span><\/p>\n

\u00b7 SMM’s audience capabilities<\/span><\/p>\n

\u00b7 Auditor Skills Certification: RICEC registration access<\/span><\/p>\n

\u00b7 Final exam (admission to written and oral exam test is subject to passing continuous assessment)<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Internal H ACCP Auditor” tab_id=”1656408259041-254f4b3f-a697″][vc_column_text]INTERNAL AUDITOR H.A.C.C.P.<\/span><\/p>\n\n\n\n\n\n\n\n\n\n

\n Description of course<\/u>
\n<\/strong>:<\/strong><\/span><\/p>\n

Internal auditors either in management systems or accreditation systems if not performed appropriately risk being a formal obligation that does not provide information on company trends and thus does not give an added value. AQSCERT, the Certification and Inspection Body, offers this training course for Internal Auditors on the HACCP System.<\/span><\/td>\n<\/tr>\n

Objectives<\/u><\/strong><\/span><\/p>\n

\u2022Knowledge of techniques for the correct use of internal audits as an instrument<\/span><\/p>\n

Risk management.<\/span><\/p>\n

\u25a0Providing tools for correct implementation of HACCP requirements.<\/span><\/td>\n<\/tr>\n

Content<\/u><\/strong><\/span><\/p>\n

General Concepts and Terminology<\/span><\/p>\n

\u25a0 HaCCP overview<\/span><\/p>\n

\u25a0 Management of non-conformities and corrective actions<\/span><\/p>\n

\u25a0 Audit by ISO 19011<\/span><\/p>\n

<\/strong><\/span><\/td>\n<\/tr>\n

Structure<\/strong>:<\/strong> Lectures in the hall; debates; Presentation of case studies, teamwork<\/span><\/p>\n

\u25a0 Lecturers<\/strong>: Lead qualified aqscert auditors<\/span><\/p>\n

\u25a0 Didactic materials<\/strong>: Printed copies of the above materials: forms for exercise; a copy of the HACCP standard<\/span><\/p>\n

\u25a0<\/strong> Duration<\/strong>: 2 days \u2013 16 hours<\/span><\/p>\n

<\/strong><\/span><\/td>\n<\/tr>\n

\u25a0
\n Who it addresses<\/u>
\n<\/strong>: All companies, certified or not. Auditor and general staff seeking to expand his knowledge. Students studying in the field of food safety (food technology, biotechnology, chemistry.. etc)<\/span><\/p>\n

\u25a0
\n Preliminary plea<\/u>
\n<\/strong>: None in particular<\/span><\/td>\n<\/tr>\n

\u25a0 Exam:<\/strong> Exam at the end of the written course.<\/span><\/p>\n

\u25a0 Evidence<\/strong>: Evidence of participation from AQSCERT and for successfully passing the exam at the end of the course, “HaccP Internal Auditor”<\/strong> Certificate<\/span><\/td>\n<\/tr>\n

\u25a0 Registration fee<\/strong>:<\/span><\/p>\n

Single participation: By calendar Discounts for group registrations from the same company. The fee of participation includes didactic materials and working lunches.<\/span><\/p>\n

\u25a0 Registration mode<\/strong>: For registration in these courses it is necessary to fill out Form I<\/span><\/p>\n

Registration, specifying the dates you are interested in. The number of participants in a course is minimum 12 persons to 20 persons maximum. AQSCERT reserves the right to cancel courses in case the minimum number of participants is not reached. More detailed information will be communicated to participants at least 5 working days before the start of the course.<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Auditor Lead Auditor ISO 22000″ tab_id=”1656408369396-fe415eaa-f74f”][vc_column_text]AUDITOR LEAD AUDITOR ISO 22000<\/span><\/p>\n\n\n\n\n\n\n\n\n\n

\n Description of course<\/u>
\n<\/strong>:<\/strong><\/span><\/p>\n

Increasing skills is a must for every professional: auditors are not exempt from these needs. The ISO 22000:2005 scheme for hygiene safety is the natural market for already qualified auditors in other systems such as quality and environment and working in the ashtray sector. AQSCERT, the Certification and Inspection Body, offers these training courses dedicated to auditors who wish to extend their qualifications in ISO 22000 for Hygiene Safety Management.<\/span><\/td>\n<\/tr>\n

Objectives<\/u><\/strong><\/span><\/p>\n

Iso 22000:2005 (Food Safety Management System)<\/span><\/p>\n

\u25a0 Integration of auditing skills under ISO 22000:2005 and their application in practice.<\/span><\/p>\n

\u25a0 Expansion of an Auditor’s qualifications from other schemes in the ISO 22000:2005 scheme.<\/span><\/p>\n

<\/u><\/span><\/td>\n<\/tr>\n

Content<\/u><\/strong><\/span><\/p>\n

\u25a0 22000 Series<\/span><\/p>\n

\u25a0 Requirements of standard 22000: 2005<\/span><\/p>\n

\u25a0 Practical cases<\/span><\/p>\n

\u25a0 Food legislation<\/span><\/p>\n

\u25a0 Hygiene-sanitary audit techniques<\/span><\/p>\n

<\/strong><\/span><\/td>\n<\/tr>\n

\u25a0 Structure:<\/strong> lecture in the halls; Internships; practical exercises; presentation of case studies.<\/span><\/p>\n

\u25a0 Lecturer:<\/strong> Lead auditor Of ISO 22000:2005 Standard<\/span><\/p>\n

\u25a0 Didactic materials:<\/strong> Printed copies of the above materials: forms for exercise; copy of series 22000<\/span><\/p>\n

\u25a0 Duration<\/strong>: 3 days \u2013 24 hours; Frequency<\/span><\/p>\n

<\/strong><\/span><\/td>\n<\/tr>\n

\u25a0 Who it addresses<\/strong>: Qualified auditors in other systems (as of 19011) who want to expand their control capabilities to third parties in the hygiene security management system.<\/span><\/p>\n

\u25a0 Preliminary requirement<\/strong>: Successfully passing a 40-hour AQSCERT course.<\/span><\/td>\n<\/tr>\n

\u25a0 Exam<\/strong>: Exam at the end of the written course.<\/span><\/p>\n

\u25a0 Certificates\/proofs<\/strong>: Proof of participation from AQSCERT (Iso 22000:2005 lead auditor) and for successfully passing the exam at the end of the course, Certificate “Auditor\/Lead Auditor” according to ISO 22000:2005 Standard<\/span><\/td>\n<\/tr>\n

\u25a0 Registration fee<\/strong>:<\/span><\/p>\n

Single participation: By calendar Discounts for group registrations from the same company. The fee of participation includes didactic materials and working lunches.<\/span><\/p>\n

\u25a0 Registration mode<\/strong>: For registration in these courses it is necessary to fill out Form I<\/span><\/p>\n

Registration, specifying the dates you are interested in. The number of participants in a course is minimum 12 persons to 20 persons maximum. AQSCERT reserves the right to cancel courses in case the minimum number of participants is not reached. More detailed information will be communicated to participants at least 5 working days before the start of the course.<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”Auditor OHSAS 18001″ tab_id=”1656408403453-cb3fe30c-6d58″][vc_column_text]Auditor\/ Lead auditor OHSAS 18001:2007<\/span><\/p>\n\n\n\n\n\n\n\n\n\n
LEAD AUDITOR OF HEALTH MANAGEMENT AND SAFETY SYSTEM AT WORK<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 3 days (24 hours)<\/strong><\/span><\/td>\n<\/tr>\n
Recognized didactics for certification at RICEC. Our audit management systems courses are modular. The module is pre-emptive and in common with three Management System courses, therefore this training course aims at qualification of system auditors for each certification scheme must be present and have passed at least once.<\/span><\/p>\n

Successful completion of comprehensive training on the eligibility of the System Auditor for a scheme will be possible to participate in the only specialization module in relation to other schemes.<\/span><\/p>\n

The educational content of our courses for Management System Auditors and final exams are recognized for ricec certification goals for the same auditor management systems.<\/span><\/td>\n<\/tr>\n

OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
The course has the following objectives:<\/span><\/p>\n

\u00b7 To be able to correctly interpret the requirements and implementation of OHSAS 18001:2007 in the context of auditing part three.<\/span><\/p>\n

\u00b7 To acquire the methodology for planning and implementing SMS audits according to the process and in accordance with the requirements of ISO\/IEC 17021:2015 standard;<\/span><\/p>\n

\u00b7 To learn teaching methods to require audit evidence necessary to assess the degree of compliance with OHSAS 18001:2007;<\/span><\/p>\n

\u00b7 Be able to communicate effectively during interviews and through written audit accounts and presentation of the overall audit results of OHSAS 18001:2007;<\/span><\/td>\n<\/tr>\n

CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
The course is theoretical and practical type, with practical audit objective exercises for the Health and Safety System at Work.<\/span><\/p>\n

The main topics include:<\/span><\/p>\n

\u00b7 Legislation applicable to auditing the third part of SMS<\/span><\/p>\n

\u00b7 EA accreditation and SMS certification sectors<\/span><\/p>\n

\u00b7 Terms and definitions<\/span><\/p>\n

\u00b7 Mandatory and Applicable Legislation<\/span><\/p>\n

\u00b7 SGS processes and their interactions<\/span><\/p>\n

\u00b7 The rating of mc,<\/span><\/p>\n

\u00b7 PDCA applied to SMS audit<\/span><\/p>\n

\u00b7 Competence of the leadership team and auditors<\/span><\/p>\n

\u00b7 Audit plan<\/span><\/p>\n

\u00b7 Initial meeting<\/span><\/p>\n

\u00b7 Role of checklist<\/span><\/p>\n

\u00b7 Their conformities and classifications.<\/span><\/p>\n

\u00b7 Independent Audit Report<\/span><\/p>\n

\u00b7 Final meeting<\/span><\/p>\n

\u00b7 Analysis of causes<\/span><\/p>\n

\u00b7 Corrective actions<\/span><\/p>\n

The course includes group work sections and exercises: The work will be attributed as a valid result (continuous assessment) for admission to the written exam and the oral exam which will be carried out at the end of the course.<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”AUDITOR FOR ENERGY MANAGEMENT SYSTEMS ISO 50001:2011″ tab_id=”1656408437362-8123ba2e-f1a1″][vc_column_text]AUDITOR FOR ENERGY MANAGEMENT SYSTEMS ISO 50001:2011<\/span><\/p>\n\n\n\n\n\n\n\n\n\n
AUDITOR FOR ENERGY MANAGEMENT SYSTEMS ISO 50001:2011<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 3 days (24 hours) \u2013<\/strong><\/span><\/td>\n<\/tr>\n
The course title is the preceding frequency of the course:<\/strong><\/span><\/p>\n

Auditor Management System: Audit Methodology or other course of UNI EN ISO 19011:2012<\/span><\/td>\n<\/tr>\n

OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
The course aims to develop practical skills that a professional Auditor\/Chief Auditor should possess to assess the degree of compliance, efficiency and improvement of the Energy Management System.<\/span><\/p>\n

The course will include the following objectives:<\/span><\/p>\n

\u00b7 Opportunity of participants with the knowledge necessary to assess the effectiveness of an Energy Management System<\/span><\/p>\n

\u00b7 Fully understand the meaning of the terminology used (aspects, impacts, legal requirements and regulations, etc.)<\/span><\/p>\n

\u00b7 Learn the correct interpretation of ISO 50001 requirements<\/span><\/p>\n

\u00b7 The methodology for planning and implementing audits of the efficient and efficient energy management system.<\/span><\/p>\n

\u00b7 Teaching methods to require audit evidence needed to assess the degree of compatibility of the ENERGY MANAGEMENT SYSTEM of ISO 50001 standard<\/span><\/p>\n

\u00b7 Be able to communicate effectively during interviews and through written audit accounts<\/span><\/p>\n

\u00b7 To present the general audit results<\/span><\/td>\n<\/tr>\n

CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
The duration of the course is 24 hours, theoretical and practical, and it offers the application of practical and theoretical exercises<\/span><\/p>\n

The main topics include<\/span><\/p>\n

\u00b7 The scenario and context in which is developed is ISO 50001:2011<\/span><\/p>\n

\u00b7 Unit of employees and production of energy<\/span><\/p>\n

\u00b7 Basic formulas and numbers to remember the energy field<\/span><\/p>\n

\u00b7 Unit parameters and practical use parameters in the energy sector<\/span><\/p>\n

\u00b7 Overview of measurement systems<\/span><\/p>\n

\u00b7 Examples of energy analysis<\/span><\/p>\n

\u00b7 Climate change: greenhouse effect, Kyoto Protocol and flexible mechanisms and application exercises<\/span><\/p>\n

\u00b7 Binding legislation in the field of energy, ISO 50001:2011<\/span><\/p>\n

\u00b7 Critical issues and documentation of EnMS (Energy Management System)<\/span><\/p>\n

\u00b7 Analysis of critical points of ISO 50001:2011 and application exercises<\/span><\/p>\n

\u00b7 The course ends with administration of the written and oral exam<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”LEAD AUDITOR FOR INFORMATION SECURITY ISO 27001″ tab_id=”1656408462938-1b5c13d3-3d18″][vc_column_text]LEAD AUDITOR FOR INFORMATION SECURITY ISO 27001<\/span><\/p>\n\n\n\n\n\n\n\n\n\n
LEAD AUDITOR OF INFORMATION SECURITY MANAGEMENT SYSTEM<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 3 days (24 hours)<\/strong><\/span><\/td>\n<\/tr>\n
Our Auditor Courses on Systems Management are modulated. The module is preliminary and common for all courses in management systems, therefore, the course aims at the qualification of the System Auditor for any certification scheme which must be frequented and passed at least once.<\/span><\/p>\n

Successful completion of the complete training on the eligibility of the System Auditor for a scheme may be possible to participate only in the specialization module in relation to other schemes.<\/span><\/p>\n

Training courses for auditors on Management Systems and final exams are recognized for ricec certification goals for the same Management Systems for Auditors<\/span><\/td>\n<\/tr>\n

OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
The course has objectives<\/span><\/p>\n

\u00b7 It must correctly interpret applicable requirements and those that are extingitive from ISO\/IEC 27001:2013 in the context of auditing part three.<\/span><\/p>\n

\u00b7 To implement the appropriate methodology for effective planning and implementation of SMSI audits according to the process method and in accordance with the requirements of ISO\/IEC 27006:2011 standard of ISO\/IEC 17021:2011;<\/span><\/p>\n

\u00b7 Teaching methods to require audit evidence necessary to assess the rate of compliance of an SMSI of THE ISO\/IEC 27001:2013<\/span><\/p>\n

\u00b7 Ability to effectively communicate interviews and through written audit reports<\/span><\/p>\n

\u00b7 To know how to present the general results of the audit<\/span><\/td>\n<\/tr>\n

CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
The course is theoretical and practical, with objective exercises to teach good audit practices of Management Systems for Information Security.<\/span><\/p>\n

The main topics include:<\/span><\/p>\n

\u00b7 Applicable rules for third-party SMSI audits<\/span><\/p>\n

\u00b7 Terms and Definitions of Information Security<\/span><\/p>\n

\u00b7 Iso\/IEC 27001:2013<\/span><\/p>\n

\u00b7 Risk analysis and references to UNI ISO 31000:2010<\/span><\/p>\n

\u00b7 Effective measurements of controls and references to ISO\/IEC 27004:2009<\/span><\/p>\n

\u00b7 Checks attached to annex A<\/span><\/p>\n

\u00b7 PDCA application in SMSI audit<\/span><\/p>\n

\u00b7 Competence of team leader and auditors<\/span><\/p>\n

\u00b7 Audit plan<\/span><\/p>\n

\u00b7 Initial meeting<\/span><\/p>\n

\u00b7 Role of checklist<\/span><\/p>\n

\u00b7 Their conformities and classifications.<\/span><\/p>\n

\u00b7 Independent Audit Report<\/span><\/p>\n

\u00b7 Final meeting<\/span><\/p>\n

\u00b7 Analysis of important cases<\/span><\/p>\n

\u00b7 Corrective actions<\/span><\/p>\n

The course includes group work meetings and exercises: results (continuous assessment) valid for admission to written exam and oral exam will be given at the end of the course<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”AUDITOR LEAD FOR MANAGEMENT SYSTEMS FOR IT SERVICES ACCORDING TO ISO\/IEC 20000-1:2011″ tab_id=”1656408491065-3a3085a1-5acd”][vc_column_text]AUDITOR LEAD FOR MANAGEMENT SYSTEMS FOR IT SERVICES ACCORDING TO ISO\/IEC 20000-1:2011<\/span><\/p>\n\n\n\n\n\n\n\n\n\n
AUDITOR LEAD FOR MANAGEMENT SYSTEMS FOR IT SERVICES ACCORDING TO ISO\/IEC 20000-1:2011<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 3 days (24 hours)<\/strong><\/span><\/td>\n<\/tr>\n
Pre-conditions:<\/span><\/p>\n

Participants must have attained a qualification as Lead Auditor of each SG or participated in a course on audit techniques (ISO 19011:2011 and ISO 17021:2011). They have acquired knowledge in the IT sector, basic skills in relative processes, knowledge of the principles of the IT Management Service and iso\/IEC 20000 standards and basic knowledge of English language. The course will be conducted in Italian and some of the materials in English (IT Service Management Standards).<\/span><\/p>\n

<\/strong><\/span><\/td>\n<\/tr>\n

OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
Preparation for running the first, second and third party management systems for IT Services (ITSMS) according to ISO 20000-1:2011 StandardID<\/span><\/td>\n<\/tr>\n
CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
The course provides information and knowledge to plan and realize management systems for IT Services (ITSMS), in accordance with the requirements of ISO\/IEC 20000-1:2011, best practices of ISO\/IEC 20000-2:2012, ISO 19011:2011 and ISO 17021:2011 standard for verification of management systems.<\/span><\/p>\n

The course, which lasts three days (24 hours), provides the essential formative elements for the role-conscious Chief Auditor and provides the necessary means to perform his task as best as possible.<\/span>
\nThe course uses a combination of theoretical lectures, practical exercises and role in relation to:<\/span><\/p>\n

\u00b7 It Service Management<\/span><\/p>\n

\u00b7 Requirements of ISO\/IEC 20000-1:2011 and other ISO\/IEC 20000 family standard<\/span><\/p>\n

\u00b7 Audit Management of an IT Service Management System<\/span><\/p>\n

The course ends with an exam which if passed, can achieve the status of Iso\/IEC 20000-1:2011 Chief Assessor.<\/span><\/p>\n

The final exam is subject to continuous evaluation of each participant during exercises, topics, presentations and personal contributions<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

[\/vc_column_text][\/vc_tta_section][vc_tta_section title=”ISO 13485″ tab_id=”1656408514382-c55c0583-45bf”][vc_column_text]ISO 13485<\/span><\/p>\n\n\n\n\n\n\n\n\n\n
ISO 13485:2012<\/strong><\/span><\/td>\n<\/tr>\n
TIME:<\/strong> 2 days (16 hours)<\/strong><\/span><\/td>\n<\/tr>\n
The medical device industry, always strategic in health, is taking on importance for the large number and multiplying of products and the impacts they have on the health and well-being of the individual, as well as on healthcare costs. In a delicate context, continuous training and industry updates, and in particular, for people responsible for overseeing product quality and processes constitute an essential need to provide adequate responses and effective responses to complex Community legislation on CE markings (Directive 93\/42\/CEE, Directive 98\/79\/CEE, Directive 90\/385\/CEE).<\/span><\/td>\n<\/tr>\n
OBJECTIVES:<\/strong><\/span><\/td>\n<\/tr>\n
\u00b7 The course responds to the need to put participants in a position to adapt a Quality Management System to the specific requirements of the medical device sector, reducing in the context of a device or family of special devices. In order to ensure the completion of the funds, the course content is also related to the application instruction ISO\/TR 14969 and of course the course is completed with the presentation and discussion of risk analysis methodology in accordance with ISO 14971<\/span><\/td>\n<\/tr>\n
CONTENT:<\/strong><\/span><\/td>\n<\/tr>\n
\u00b7 Home<\/span><\/p>\n

o Medical devices, medical device categories<\/span><\/p>\n

o The general framework for the context of European national regulations<\/span><\/p>\n

\u00b7 ISO 13485, integrated with ISO\/TR 14969<\/span><\/p>\n

Compatibility with other management systems<\/span><\/p>\n

o System requirements: documentation management, policy, objectives and responsibilities, customer orientation, resource management<\/span><\/p>\n

O Design and implementation of the product and its control<\/span><\/p>\n

o Historic document design, device master record, history of record devices (Device Hystory Record)<\/span><\/p>\n

o Measurement, monitoring, improvement<\/span><\/p>\n

\u00b7 Risk analysis applies to medical devices \u2013 ISO 14971 standard<\/span><\/p>\n

\u00b7 Internal audits of a Quality Management System in accordance with ISO 13485<\/span><\/p>\n

The course has a special practical application. The applied methodology ensures active learning, with an analysis and discussion of experimental cases, sharing and dealing directly with the teacher<\/span><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

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[vc_row][vc_column][vc_tta_tour color=”peacoc”][vc_tta_section title=”Audience 9001″ tab_id=”1656407067860-ba7f1882-cd56″][vc_column_text]AUDITOR \/CHIEF AUDITOR OF THE MANAGEMENT SYSTEM: AUDIT METHODOLOGY AUDITOR \/CHIEF AUDITOR OF THE MANAGEMENT SYSTEM: AUDIT METHODOLOGY TIME: 2 days (16 hours) Updated course for new standard The implementation of the auditor\/Chief Auditor Management System training is conducted in a modular and provides for the payment of a first incoming … Continue reading Training on international standards<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_eb_attr":"","footnotes":""},"class_list":["post-8057","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/pages\/8057","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/comments?post=8057"}],"version-history":[{"count":2,"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/pages\/8057\/revisions"}],"predecessor-version":[{"id":8063,"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/pages\/8057\/revisions\/8063"}],"wp:attachment":[{"href":"https:\/\/www.aqscert.org\/en\/wp-json\/wp\/v2\/media?parent=8057"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}