Manage your QMS
-Corporate Sustainability Assurance (New)
-ISO 9001 Quality management Systems Migration
-ISO 14001 Environmental Management System
-ISO 13485 Medical Devices - Quality Management Systems MDSAP
-ISO 45001 Occupational health and safety
-R2 Recycler Responsible
- ISO 27001 International Information Security Standard
- ISO 19011 Guidelines for auditing management systems
SpinOff the solution to your ISO management
SpinOff offers a range of services to facilitate the implementation, maintenance and migration of your ISO. With more than 25 years of experience and recognition from all the domain registrars.
Whether it's for the 9001: 2015 migration or simply to perform your full enterprise risk management, SpinOff is the solution.
Looking to have your product recognized by Health Canada?
Contact us, we will help you reach your goals!
Contact us for the detail of all our trainings
Business services
Training 9001: 2015
Details: 8 hours training
Why: this training is for an understanding of the principles and concepts of the new standard before undertaking your migration Thérorie: Explanation of the requirements used in quality management and the 7 principles of quality management presented in ISO 9001
Activity: Linking the quality management system to the products and services of an organization and to your operational processes
Purpose: To enable you to master the migration of your SMQ to ISO 9001: 2015
Details: 8 hours training
Why: This risk analysis training helps to demystify the requirements of s. 6.1 of the new ISO 9001: 2015 standard.
Activity: Randomly select two processes in order to allow the Director of Quality to understand the normative methods and requirements in order to carry out his own risk assessments, validation of the FMEA or FMECA approach
Purpose: To be able to implement a risk management process
Training Risk Analysis
Gap analysis
Details: Our advisors carry out activities similar to the internal audit using the targeted standard. All of our advisors are certified chief auditors and have the experience required to file an accurate and complete report in order to allow the company to initiate corrections as necessary.
Methodology: Knowing the requirements of both standards, the current one (for which the company has the certification) and the new standard imposed, the advisor carries out an assessment similar to the internal audit activity. It validates the deviation as well as the perceived effort required to achieve normative compliance. The advisor prepares a report of the activities to be carried out in order to ensure the compatibility of the transition.
Purpose: To enable the company to assess the investment required to complete its transition to the new standard.
Turnkey Migration
Details: In addition to consulting services to alleviate the migration of your Quality Management System, our consultants will be in charge of adapting the documentation required to satisfy the normative requirements while preserving the context of the company.
Methodology: Review the existing procedures and integrate the interrelations between the processes to migrate 9001: 2015. Ensure the development of the new requirements such as the risk assessment for each of the company's processes according to the FMEA or FMEA
Objective: To obtain certification according to the new ISO.
Internal Auditor Training
Details: 16 hours training
Prerequisite: Attended Training 9001: 2015
Why: Understand the intricacies of how to perform an effective audit process in the organizational context.
Theory: Give explanation on the application of requirements statements and other elements relevant to the audit and the management system.
Activity: Putting into practice the concepts learned by the internal audit of some elements specific to the company's QMS (or case study)
Purpose: To put into practice the personal skills necessary to effectively perform a management system audit
Internal Quality Audit Phase 2
Details: All of our auditors are certified lead auditors and have the experience to file a complete and accurate report in order to allow the company to initiate corrections as necessary.
Methodology: Conduct a process audit in accordance with the normative requirements.
Purpose: Assure the availability of evidence to evaluate the effectiveness of the implementation of the processes documented in the company
Internal Quality Audit Phase 1
Details: All of our auditors are certified lead auditors and have the experience to file a complete and accurate report in order to allow the company to initiate corrections as necessary.
Methodology: Revision of your procedures migrated 9001: 2015 according to the requirements of standard 9001: 2015.
Purpose: Validation of conformity of your ISO documentation