IP&C Regulations: Product Requirements
This course aims to educate healthcare workers on the specific regulations and directives relating to the requirements they should be aware of when selecting cleaning and disinfection products.
Course overview
IP&C Regulations: Product Requirements is an online training program developed by schülke UK to educate healthcare workers on regulations relating to infection prevention and control products and what they mean in practice. The relevant European regulations and directives are covered using a combination of summaries, case studies and diagrams. The course can be completed at work or home on a variety of smart devices.
1 hour of CPD
Professional Accreditation
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Learning outcomes
On completion of thie course trainees will:
1. Have a better understanding of current regulations, directives and laws surrounding medical devices.
2. Be aware of the various classifications for medical devices and the authorisation process for products on the European market.
3. Understand which essential requirements ensure product performance and safety.
4. Recognise when a dual registration is applicable to a medical device, and understand the significance of a CE mark. -
Course content
Add members of your team, when registering for this course to save time and track their progress. Trainees will cover the following modules:
- Counterfeit Medical Devices
- Medical Device Directive
- Biocidal Products Regulation
- Dual-registration of products
- REACh guidelines
Each module is accompanied by a multiple choice test to assess the trainee's understanding of the content. When all module tests are completed the trainee will receive a personalised certificate.