First of all, take a look through these threads:
Product Realization related discussion threads. It's pretty much the same in all the standards it is in (ISO 9001, ISO 13485, etc.), but note that each may have some
additional requirements when compared to ISO 9001, for example.
Essentially you have to have a quality plan for products(s).
What Randy was trying to say is that 7.1 is sort of a "topic". It has sub-topics (aka clauses) which you must comply with. When you comply with each sub-clause you will meet the requirements of 7.1.
As to forms and such, take a look through
Quality Plan Example Files as a starter.