If a regulated party has questions about their legal obligations or responsibilities under the Act or Regulations, they should seek the advice of legal counsel.
They have been developed and are maintained by the QWP.
If further clarification is required, reference should be made to the Canadian " should be taken into account where relevant and as appropriate to the stage of development of the product.
Procedures need to be flexible to provide for changes as knowledge of the process increases, and appropriate to the stage of development of the product.
I received some IMP that had no expiry date on the packaging only on the QP release.
Our Trust policy is that every medcine must have an expiry date on it so we are wrtiing it on - what are others doing in this situation???