Training

Training of certification company Aqra certification doo  is focused on improving the products and services of our clients, and as a company we aim to present to the participants and offer rich and applicable technical training.

Aqra has local and foreign trainers who are excellent experts and have extensive and valuable experience in the field of technology and training on specific standards.

Your training request send to this address aqra@aqracertification.com


Training Plan 2018

2018 TRAINING PLAN
TRAININGPLANNED DATEPARTICIPANTS PROFILEPROJECTED SKILLS
ISO 9001:2015 TRANSITION TRAININGThose involved in the planning, implementation, protection, management or inspection of the ISO 9001: 2015 QMS may participate.Implementing a structure based on ISO 9001: 2015 will help you to carry out the continuity of your products and services and to carry out continuous improvement.

Your organization needs to acquire the skills necessary to implement the basic principles of ISO 9001: 2015. The knowledge and experience required to implement the ISO 9001: 2015 Quality Management System in practice training are communicated to participants.

ISO 14001:2015 TRANSITION TRAININGThose involved in the planning, implementation, protection, management or inspection of the ISO 14001: 2015 EMS may participate.When implementing an effective EMS, defining the basic benefits for your organization, development of the necessary plan for implementation and determination of resources,

Using good practices in practice, using proven tools and techniques, the implementation of the system, which takes into account socio-economic needs and environmental conditions, to provide products and services to meet the customer and legal environment requirements at all times,

 

ISO 13485 TRAININGQuality director, engineers, management representatives, consultant, design engineers, production managers, service managers who works on medical device field.

Engineering faculty students who wants to work on medical devices field

“ISO 13485 Implementation” training; as defined in the ISO 13485 standard for medical devices, the necessary notions to understand, develop and implement a quality management system. This training also covers the bases of the ISO 14971 standard, which includes the key principles of risk management. Experienced instructors will explain how to integrate the ISO 13485 system application into the entire operation, how to prepare for the audit, and how to obtain ISO 13485 documentation. The exercises included in the training will prepare the participants for the preparation of key requirements, the creation of documentation, the development of project plans and the preparation of a process map.
ISO 13485 LEAD AUDITOR TRAININGQuality director, engineers, management representatives, consultant, design engineers, production managers, service managers who works on medical device field.

Engineering faculty students who wants to work on medical devices field

ISO 14971 Application of Risk Management to Medical Devices Training15-16-17 January 2018Quality director, engineers, management representatives, consultant, design engineers, production managers, service managers who works on medical device field.

Engineering faculty students who wants to work on medical devices field

Definition of risk management, objectives and terminology, analysis , evaluation and control of risks, evaluation of total residual risks, effects of risk management on product life cycle, Relation between 13485 and 14971 standards
Meddev 2.7.1 Clinical Evaluation Training12-13 February 2018Quality director, engineers, management representatives, consultant, design engineers, production managers, service managers who works on medical device field.

Engineering faculty students who wants to work on medical devices field

Guidance for Clinical Evaluation of Manufacturers and Notified Bodies Subject to the Directives of Meddev 2.7.1 rev.04 93/42 EEC and 90/385 EEC, which is one of the most important topics of this training technical purpose document “and clarification of how these requirements should be met. Training will be done through example documents and records.

Required training form