Selection of a Comparator Product to be used in Establishing Interchangeability Written by AMallya on 26 July 2021.
Stakeholder’s Consultative Meeting on EAC Joint Regulatory Procedure and Sustainability Plan Written by AMallya on 07 February 2022.
Stakeholder’s Consultative Meeting on EAC Joint Regulatory Procedure and Sustainability Plan Written by AMallya on 09 February 2022.
Submission of Active Finished Pharmaceutical Products (FPP) to the EAC Written by AMallya on 26 July 2021.
Submission of Active Pharmaceutical Ingredient Master File (APIMF) to the EAC Written by AMallya on 26 July 2021.
Summary Technical Documentation (STED) for In-Vitro Diagnostic Medical Devises Dossier Written by AMallya on 26 July 2021.
WHO Global Model Regulatory Framework for Medical Devices including In Vitro Diagnostic Medical Devices Written by AMallya on 26 July 2021.
Withdrawal of Applications for Registration of Medicinal Products submitted through EAC Joint Assessment Pathway with pending query responses for more Written by AMallya on 16 May 2022.