Mediteq offers training
in the medical device and in-vitro diagnostic area.
We provide training with enthusiasm and energy, always with your needs in mind!
Mediteq offers training on several topics related to regulatory requirements and quality for medical devices. We deliver both basic and in-depth training as well as workshops. Our training is customized to various types of actors in the industry such as manufacturers, healthcare providers, subcontractors, suppliers, consultants, distributors, and others.
Mediteq offers training in the following areas for medical device companies:
- CE marking
- Regulations – MDR, IVDR and CFR
- Management systems
- Internal auditing
- Risk management
- Product development
- Software development
- Clinical evaluation and follow-up
The scope and length of our training vary from a half-day introduction to several days of in-depth training customized to the participants’ prerequisites and needs. The training is tailored to your organization and product type, e.g various requirements for implants, electrical products, or software products. Mediteq can conduct the training on-site at your facility or through us, and we also offer distance learning through digital tools.
Our trainers educate with joy and energy, and always keep your needs in focus! We look forward to teaching you and your colleagues more about our favorite topics – regulations, legal requirements, and standards for medical devices.
The length of the training can vary from a few hours to several days, and we can perform it on-site at your facility or in our premises. Mediteq can also offer remote training from our webstudio.
Our trainers have many years of practical experience in the medical device industry and keep up-to-date in the regulatory area with engagement in standardization and industry organizations.
If you want to discuss your training needs with us, please contact us for customized training.
Mediteq offers a digital training course in Swedish for requirements and regulations of medical devices. In 29 web-based lessons we present the basics of MDR 2017/745 and provide an overview of the requirements for CE marking a medical device and to be sold in EU. Our e-learning provides you as a participant with the opportunity for flexible and time-efficient competence development. For organizations and companies, our e-learning is a cost-effective way to offer competence development to all employees, either at individual occasions or long-term.
The e-learning includes:
- 29 web-based lessons in Swedish
- Knowledge questions after each lesson
- Digital material to download
- Certificate of completion
For more information and ordering of e-learning, please contact us at firstname.lastname@example.org
Mediteq has been a training leaders for SIS, Svenska Institutet för Standarder since 2015. Here you can learn the basics of MDR or IVDR regulations, management systems, internal auditing, risk management and medical software.