What does a Third Party need to consider, when creating MSF devices for sale?
- Is an approval from Melda needed?
- Do they need to pay a fee to Melda?
- Are they allowed to use samples included in the MSF / MDrummer in their devices?
- Anything else to be cosidered like restrictions or any overall rules?
- Is there an official information from Melda, where the above questions are already answered?
Thanks in advance for answers or hints.
