This year The Jordan Food & Drug Administration (JFDA) has updated their Directives for The Analysis of Drugs and The Regulations for the Drug Release; to focus more on the quality, safety & efficacy of medications after being marketed and distributed to the retail pharmacies & hospitals.
The update was emerged from the need to control the medications throughout the whole supply chain, to ensure the patients receive the most effective and safe medications.
We were honored to be part of the technical committee responsible for the new updates, and to ensure that all stakeholders are aligned with the new procedures and regulations, we’ve gathered all parties on the same table for discussion, with the kind cooperation of The Jordan Food & Drug Administration (JFDA) on Nov 4 2024.
The workshop “Drug Release and QC lab Analysis Regulations & Updates at the JFDA” discussed all the needed details for the testing of medications, starting from their Primary Testing after registration, ending in the post marketing surveillance throughout the supply chain.
All the appreciation & gratitude for our colleagues at The Jordan Food & Drug Administration (JFDA) under the leadership of H/E Dr. Nizar Muheidat, for the continuous cooperation & support.
Special thanks to Dr. Amal Abu-Rub (The head of The Lab Directorate at the JFDA) and to the amazing speakers Dr. Mais Al-Khraisha, Dr. Hiba Abdel-Rahim, Dr. Yazan Al-khateeb, Dr. Huda Qurani, Dr. Bayan Momani, Dr. Manal Jafary, Dr. Nisreen Harasis & Dr. Israa Basheer from both the Lab & Drug Directorates at the JFDA.
The workshop was attended by experienced professionals from The Jordan Food & Drug Administration team, distinguished members from DOA, and representatives from various multinational & local pharmaceutical companies and distributors, all of whom contributed to the rich discussions and insights gained during the event.
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