| Process Flow of Importation of Medical Products Published | Communication to industry | 17/07/2023 | 1 | Inspectorate and good manufacturing practices, Regulatory Compliance | pdf | Download | communication-to-industry | inspectorate-and-good-manufacturing-practices regulatory-compliance |
| Retention Fee Notification – 9 June 2022 | Communication to industry | 24/06/2022 | 1 | Biological Medicines, General ECTD & human medicines, Inspectorate and good manufacturing practices, Medical Devices | pdf | Download | communication-to-industry | biological-medicines-evaluation-and-research general-ectd-human-medicines-guidelines inspectorate-and-good-manufacturing-practices medical-devices |
| Communication to Industry – Applications for GMP and CPP Certificates | Communication to industry | 30/06/2022 | 1 | Inspectorate and good manufacturing practices | pdf | Download | communication-to-industry | inspectorate-and-good-manufacturing-practices |
| Submission of Post-Importation Testing Exemption requests for Biological and Biosimilar Medicines | Communication to industry | 24/03/2022 | 1 | Biological Medicines, Inspectorate and good manufacturing practices | pdf | Download | communication-to-industry | biological-medicines-evaluation-and-research inspectorate-and-good-manufacturing-practices |
| SAHPRA survey to determine company turnover | Communication to industry | 31/03/2021 | 1 | Inspectorate and good manufacturing practices, Licencing | pdf | Download | communication-to-industry | inspectorate-and-good-manufacturing-practices licencing |
| GMP CERTIFICATES FOR CANNABIS CULTIVATED BY CULTIVATORS HOLDING A SECTION 22C(1)(b) LICENCE (LICENCE TO CULTIVATE CANNABIS FOR THE PURPOSES OF PRODUCING SCHEDULED SUBSTANCES) | Communication to industry | 25/03/2021 | 1 | Inspectorate and good manufacturing practices, Licencing | pdf | Download | communication-to-industry | inspectorate-and-good-manufacturing-practices licencing |
