GMP pharmaceutical packaging record sheet to do what can be perfect?

How easy is it to be "perfect"? The following are a few points of view, for reference only:

1. Printed packages (labels, instructions, boxes, certificates of conformity) counted issued,

2. Printed packages double double-locked control, especially labels and instructions

3. Each use of the completion of the calculation of the rate of receipt and balance, the balance rate should be 100%

4. Before the use of packages for every type of sample should be checked, including text, version, paper, and color.

5. Supplier audits should be conducted for suppliers of printed packages.

6. All printed packages with lot numbers, expiration dates, and production dates should be counted and destroyed.

All of the above should be documented with operator, reviewer and QA audit and date recorded.

Any deviations that occur should be registered and investigated.

Get it right and then think about "perfection".