Application for inclusion, change or deletion of a medicine.

An ADR is a response to a medicine which is noxious and unintended, and which occurs at normal doses.

This application enables suppliers of pharmaceuticals and medical supplies to be pre-qualified for supplying medical products to OECS/PPS. Information derived from forms submitted by potential suppliers will be used to evaluate companies, assess their business history, and/ or manufacturing and production capabilities consistent with GMP and/or ISO standards.