guidelines for each of the countries. 9. Ensure internal cGMP inspections are regularly carried out. 10 products are registered. 15. Conducting Internal Quality Audits (IQA) and facilitating the addressing of non-conformances and observations raised in such audits. 16. Raising of standard operating procedures (SOPs) medicinal products and detect any change to their risk-benefit balance at periods specified by the Authority activities arising from dossier purchases and from internally developed products (Varichem) so as to ensure
guidelines for each of the countries. 9. Ensure internal cGMP inspections are regularly carried out. 10 products are registered. 15. Conducting Internal Quality Audits (IQA) and facilitating the addressing of non-conformances and observations raised in such audits. 16. Raising of standard operating procedures (SOPs) medicinal products and detect any change to their risk-benefit balance at periods specified by the Authority activities arising from dossier purchases and from internally developed products (Varichem) so as to ensure
and accurate remedy of faulty SMEG products for internal and external customers. Complete required administration