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Consultation Count: 291

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Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Radioactive Materials and Pharmaceutical products Used in Nuclear Medicine

This guideline provides a regulatory framework for the import of radioactive materials and pharmaceutical products used in nuclear medicine. It ensures that all imported products comply with quality, safety, and efficacy standards, are handled, transported, and used in accordance with national health and regulatory requirements, protecting public health and safety, and specifies the import requirements for these products.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

104
2
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Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Narcotic Substances, Psychotropic Agents, and Narcotic Preparations Listed in the Schedules of Narcotic Substances, Psychotropic Agents, and Chemical Precursors Supplementing the Narcotic and Psychotropic Substances Law No. 23 of 2026

This guideline provides a regulatory framework for the import of narcotic substances, psychotropic agents, and narcotic preparations listed in the schedules of narcotic substances, psychotropic agents, and chemical precursors under Law No. 23 of 2026. It ensures that all imported substances are used safely and legally, in compliance with national and international regulations, protecting public health and preventing misuse, and specifies the import requirements for these substances.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

146
5
More Details

Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Personal Parcels

This guideline provides a regulatory framework for the import of personal parcels, ensuring that all items entering the country comply with national health, safety, and regulatory standards. It provides a framework to monitor and control their contents, facilitates lawful and safe importation, and specifies the import requirements for these parcels.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

80
0
More Details

Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Medicines and Pharmaceutical products Containing Vitamins or Minerals, Natural Products, Infant Formulas and Special Formulas, Their Dietary Supplements, Sera and Vaccines of All Types, Plasma and Its Derivatives Imported as Donations

This guideline provides a regulatory framework for the import of medicines and pharmaceutical preparations containing vitamins or minerals, natural products, infant formulas, special formulas, their dietary supplements, sera, vaccines, plasma, and its derivatives when imported as donations. It ensures that all imported products comply with quality, safety, and efficacy standards while adhering to national health and regulatory requirements and specifies the import requirements for these products.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

123
0
More Details

Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Registered Medicines and Pharmaceutical products Containing Vitamins or Minerals, Natural Products

This guideline provides a regulatory framework for the import of registered medicines and pharmaceutical products containing vitamins, minerals, natural products. It ensures that all imported products comply with quality, safety, and efficacy standards while adhering to national health and regulatory requirements, and specifies the import requirements for these products.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

144
6
More Details

Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Unregistered Medicines and Pharmaceutical Products Containing Vitamins or Minerals, Natural Products, for the Purposes of clinical Studies, Bioequivalence Studies, Registration, and Research & Development

This guideline provides a regulatory framework for the import of unregistered medicines and pharmaceutical products containing vitamins, minerals, natural products for the purposes of clinical studies, bioequivalence studies, registration, and research & development. It ensures that all imported products meet quality, safety, and efficacy standards, while complying with national health and regulatory requirements and specifying the import requirements for these products.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

107
1
More Details

Agency Name: Jordan Food and Drug Administration

Guideline for the Import, Export, and Entry of Medicines Containing Narcotic Substances and Psychotropic Agents for Personal Use

This guideline provides a regulatory framework for the import, export, and entry of medicines containing narcotic substances and psychotropic agents for personal use and accompanied by passengers. It ensures their safe and legal use, while complying with health and regulatory requirements and protecting individuals and the community from the risks associated with these substances.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

74
0
More Details

Agency Name: Jordan Food and Drug Administration

Guideline for the Import of Raw Materials, Packaging Materials, and Empty Gelatin Capsules Used in the Production of Medicines and Pharmaceutical Products Containing Vitamins or Minerals, as well as Natural Products

This guideline provides a regulatory framework for the import of raw materials, packaging materials, and empty gelatin capsules used in the production of medicines and pharmaceutical Products. It ensures the quality, safety, and efficacy of all imported materials, while complying with health and regulatory requirements, monitoring both commercial and non-commercial use, and specifying the import requirements for these materials.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

82
0
More Details

Agency Name: Jordan Food and Drug Administration

Instructions for Importing Medicines and Related Products

These instructions are titled “Instructions for the Import of Medicines and Related Products for the Year 2026” and shall be effective from the date of their publication in the Official Gazette. These instructions apply to all medicines and pharmaceutical products containing vitamins or minerals, natural products, infant formulas and special formulas, their dietary supplements, sera and vaccines of all types, plasma and its derivatives, allergy preparations, semi-finished products, raw materials, packaging materials, radioactive materials used in nuclear medicine, pharmaceutical products used in nuclear medicine, free medical samples of drugs and pharmaceutical products, unregistered medicines and pharmaceutical products in non-commercial quantities for the purposes of drug studies, research and development, registration purposes, the import of personal parcels, and the import of donations.

Consultation Period

26/03/2026 - 26/04/2026

Consultation Status

Closed

Closed

167
6
More Details

Agency Name: Jordan Food and Drug Administration

Guideline on Good Pharmacovigilance Practice (GVP) IN Jordan (for pharmaceutical products)

This document provides guidance on the application of good pharmacovigilance practice in the Hashemite Kingdom of Jordan. It represents the first version of the Jordanian guidelines for good pharmacovigilance practices. The legal framework for pharmacovigilance of pharmaceutical products for human use, including biological products, in Jordan is given in the pharmacovigilance regulation for the year of 2016. This guideline is intended to facilitate the performance of pharmacovigilance activities in Jordan and applies on marketing authorization holders. The Jordan food and Drug Administration (JFDA) has a core role in coordinating these activities. Additionally, the Jordanian legislations impose responsibility for pharmacovigilance, together with specific obligations (i.e. in terms of tasks and responsibilities), on marketing authorization holders. This guideline is based on the European guidelines for good pharmacovigilance practices and Arab guidelines for good pharmacovigilance practices, this does NOT undermine the right of JFDA to have additional or sometimes changed requirements. Multinational marketing authorization holders shall be attentive to these national requirements and bring the attention of their headquarters to them, consequently, take the necessary measure to comply.

Consultation Period

24/03/2026 - 24/04/2026

Consultation Status

Closed

Closed

844
21
More Details

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