Modules
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Learning Outcomes
After completing the modules in this eLearning course, you will be able to:
MODULE 01 - EU RoHS overview and requirements
- Outline the intent and goals of the RoHS Directive No 2011/65/EU;
- Differentiate how Directive 2011/65/EU (RoHS 2) differs from Directive 2002/95/EC (RoHS 1);
- Identify substance restrictions and exemptions;
- Explain the scope of products RoHS covers;
- Describe how Directive 2011/65/EU implements CE marking and conformity requirements
- Summarise obligations for manufacturers, distributors and importers
MODULE 02 - Beyond the basics
- Describe the scope clarifications and corrections (Directive 2017/2102
- Demonstrate how to track and monitor exemption renewal and new exemption request applications
- Outline current substances under review for possible restriction, the list of substances to be reviewed and aspects of the substance review methodology
- Navigate article 24, the RoHS recast process and its status
- Explain the place of RoHS among the EU substance restriction pantheon for products
- Identify official sources of support from the European Commision
MODULE 03 - Compliance with EU RoHS
- Identify the required aspects of technical documentation as defined by Decision No 768/2008/EC and the RoHS Harmonised Standard
- Explain why using the harmonised standard is preferable to using Module A of Decision No 786/2008/EC
- Outline the four tasks involved in producing technical documentation for RoHS
- Describe the required content for a formal EU Declaration of Conformity
- Demonstrate control of series production