For new submission, there’s no problem.
For already registered product, you have to let us know when you will start to apply the change (example: for current PO etc..) so we can inform the customer if required.
Also, may I remind FCP to inform IRA for any changes that production or QA will do on any product specification so IRA can check if we need to submit any amendment in the country or not. Because we already encountered some problem on the capsule of the quoted products below for Sudan on which the final description of the finished goods does not tally with the provided CA of FCP on the PO of customer which resulted the rejection of product by the QC lab of Sudan FDA.
We do not want this kind of problem to happen again. So we will highly appreciate FCP’s cooperation on this.
Aisha