Home Study: Six Boxes – Smart Beginners CE Self-Certification Course
Learn how to do CE marking yourself and cut the 3rd party from CE certification
The Six Boxes Smart Beginners CE Self-Certification Course
You can continue to burn hours searching for CE marking information on the Internet, only to find information that is fluffy, incomplete and totally scattered. You can choose to trust that the costly services proposed by third party test laboratories and certification bodies are really in your company’s best interest.
But, if you want to take control over your CE marking projects…if you want to start with CE marking today…if you want to complete the process in as early as one week…and if you want to save a substantial amount of money in the process, The Six Boxes Smart Beginners CE Self-Certification Course is your best option.
CE MasterMind Club
CE MasterMind Club
Image a place where like-minded professionals just like you meet every day to discuss CE certification. Where you can find a treasure of information and where topics like directives, standards, testing, Technical File, users manuals are explained in great detail. Where you have direct access to the experts and you can ask them your questions. Well, stop imagining. If you have read the E-book ‘10 Clues About CE Marking 3rd Parties Don’t Want You to Know’, your next step is the CE MasterMind Club.
CE Marking Logo + Template EC Declaration of Conformity
Declaration of Conformity
Have you been struggling with the question what information has to be included in the EC Declaration of Conformity? And in what format the document should be? Have you been searching for the CE marking logo to put on your product? This package provides you an easy editable template of the Declaration of Conformity in the correct format. And we included the CE logo in various graphical file formats. A download link for the package is delivered immediately upon order. In 5 minutes you can be ready.
Medical Devices Complete CE Documents Kit
Looking for CE Marking a medical device? The process starts with reading the Medical Devices Directive (93/42/EC) and by applying the requirements written there. This can be a tedious process, because the text of the Medical Devices Directive has been amended several times. For your convenience we have a compiled a kit of important documents that you require in order to CE Mark medical devices.
