The main focus of this session will be to share our expertise and experience of CPR now that it has been up and running for a full year.
As well as a refresher on the requirements and implementation of the scheme, we will share our insights and experience of CPR to help you achieve regulatory compliance. We will cover the responsibilities and obligations of all parties in the supply chain and also share our observations on the results being achieved, what is influencing them and how this affects you.
Location: BASEC, Presley House, Presley Way, Crownhill, Milton Keynes MK8 0ES
(Minimum number for this course is 6 people.)
This typical 1/2 day course content includes:
- Introduction and scope of the course
- Scope and requirements of CPR
- Reaction to fire vs Resistance to fire
- Assessment and verification of constancy of performance systems
- Role of Notified Bodies
- Manufacturer / distributor / Notified Body duties & responsibilities
- Classification and classes / additional classifications
- Documentation requirements - market surveillance
- Requirements of EN 50575, EN 13501-6 and CLC/TS 50576
- Technical documentation - Test Reports, Classification Reports & DoPs
- Classifications for the supply chain
- Summary of test methods and Classification criteria for Classes Aca-Fca
- Regulatory and end-user requirements
- Lessons learnt
- Drafting Declarations of Performance (DoP) and labelling
- Responsibilities of manufacturers and distributors
- The types of results being achieved and what is influencing them
- Multi-Listing Classification Reports explained
- Options for dealing with old stock
- Questions and answers – open forum
- CPR testing in action - tour of the laboratory
