[vc_row][vc_column][vc_custom_heading text=”CLICK ON THE 2 TABS BELOW TO ACCESS OR DOWNLOAD GUIDELINES” font_container=”tag:h2|font_size:18|text_align:left” use_theme_fonts=”yes”][vc_empty_space][vc_single_image image=”2266″ img_size=”full”][/vc_column][/vc_row][vc_row][vc_column width=”5/6″][vc_tta_tabs active_section=”2″][vc_tta_section i_icon_fontawesome=”fas fa-download” add_icon=”true” title=”Marketing Authorisation” tab_id=”1679437850153-354d46c5-703d”][vc_btn title=”Guidelines on the Application for Grant of Marketing Authorisation of Nutritional Supplements and Feed Additives for Animal Use in Zambia” color=”black” i_icon_fontawesome=”far fa-file-pdf” css=”” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2025%2F08%2FPub-VET_GUD_001_Guidelines-on-the-Application-for-Grant-of-Marketing-Authorisation-of-Nutritional-Supplements-and-Feed-Additives-for-Animal-Use-in-Zambia1.pdf”][vc_btn title=”Quality Information Summary (QIS)” color=”black” i_icon_fontawesome=”far fa-file-pdf” css=”” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2025%2F07%2FZAMRA-QIS.pdf”][vc_btn title=”Application for Grant of Marketing Authorisation of Cosmetics for use in Zambia” color=”black” i_icon_fontawesome=”far fa-file-pdf” css=”” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2025%2F06%2FAPPLICATION-FOR-GRANT-OF-MARKETING-AUTHORISATION-OF-COSMETICS-FOR-USE-IN-ZAMBIA.pdf”][vc_btn title=”Requirements for the Listing of Cosmetics” color=”black” i_icon_fontawesome=”far fa-file-pdf” css=”” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2025%2F06%2FREQUIREMENTS-FOR-THE-LISTING-OF-COSMETICS.pdf”][vc_btn title=”Guidelines On Application for Grant Of Marketing Authorisation Of NON-IVDS” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2024%2F07%2FGUIDELINES-ON-APPLICATION-FOR-GRANT-OF-MARKETING-AUTHORISATION-OF-NON-IVDS.pdf”][vc_btn title=”Medical Gloves Guidelines” color=”black” i_icon_fontawesome=”far fa-file-pdf” css=”” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2024%2F07%2FMedical-Gloves-Guidelines-Final-1.pdf”][vc_btn title=”Guildlines of Traceability of Medicines” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuildlines-of-Traceability-of-Medicines.pdf”][vc_btn title=”Guidelines on Recall of Medicines and Allied Substance” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-on-Recall-of-Medicines-and-Allied-Substance.pdf”][vc_btn title=”Template for comments on Guidelines on Identification and Labelling of Medicines and Allied Substances and Master Data Sharing” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FTemplate-for-comments-on-Guidelines-on-Identification-and-Labelling-of-Medicines-and-Allied-Substances-and-Master-Data-Sharing.pdf”][vc_btn title=”Guildlines on Grant of Marketing Authorisation for Cosmetics” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F07%2FZAMRA-Cosmetic-Guidelines-22Mar2023-v.LC-final-1.pdf”][vc_btn title=”Guidelines on Renewal for Marketing Authorisation of Medicines and Allied Substances-ZAMRA_2019v2″ color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F05%2FGuidelines-on-Renewal-for-Marketing-Authorisation-of-Medicines-and-Allied-Substances-ZAMRA_2019v2.docx”][vc_btn title=”Guidelines on Identification and Labelling of Medicines and Allied Substances and Master Data Sharing” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FTemplate-for-comments-on-Guidelines-on-Identification-and-Labelling-of-Medicines-and-Allied-Substances-and-Master-Data-Sharing.pdf”][vc_btn title=”Application for Grant of Marketing Authorisation of In-Vitro Diagnostic Devices for Human-v1″ color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Grant-of-Marketing-Authorisation-of-In-Vitro-Diagnostic-Devices-for-Human-v1.pdf”][vc_btn title=”Guidance on submission of applications for Marketing authorisation in CTD format: Quality” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidance-on-submission-of-applications-for-Marketing-authorisation-in-CTD-format-Quality.pdf”][vc_btn title=”Guidelines for grant of Marketing Authorisation of in-vitro diagnostic devices for Human use” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-grant-of-Marketing-Authorisation-of-in-vitro-diagnostic-devices-for-Human-use.pdf”][vc_btn title=”Application for Marketing Authorisation of a Human Medicine for Human Use – Stability” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F05%2FMarketing-Authorisation-STABILITY-GUIDELINES.pdf”][vc_btn title=”Preparation and submission of Dossiers in Common Technical for Registration Quality” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FPreparation-and-submission-of-Dossiers-in-Common-Technical-for-Registration-Quality.pdf”][vc_btn title=”Application for Grant of Marketing Authorisation of Antiseptics and Disinfectants” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Grant-of-Marketing-Authorisation-of-Antiseptics-and-Disinfectants.pdf”][vc_btn title=”Application for Marketing Authorisation CTD Format – Human Medicines” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Marketing-Authorisation-CTD-Format-Human-Medicines.pdf”][vc_btn title=”Detecting and Reporting Adverse Drug or Vaccine Reactions and Events” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FDetecting-and-Reporting-Adverse-Drug-or-Vaccine-Reactions-and-Events.pdf”][vc_btn title=”Guidelines for In-vitro Diagnostic Medical Device Market Authorisation” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-In-vitro-Diagnostic-Medical-Device-Market-Authorisation.pdf”][vc_btn title=”Essential Principles of Safety and Performance of Medical Devices-v1″ color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FEssential-Principles-of-Safety-and-Performance-of-Medical-Devices-v1.pdf”][vc_btn title=”Guidelines for Label and Instructions For Use for Medical Devices” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-Label-and-Instructions-For-Use-for-Medical-Devices.pdf”][vc_btn title=”Guidelines on the Principles of Medical Devices Classifications-v1″ color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-on-the-Principles-of-Medical-Devices-Classifications-v1.pdf”][vc_btn title=”Amendment for Marketing Authorisation – Human Medicines” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FAmendment-for-Marketing-Authorisation-Human-Medicines.pdf”][vc_btn title=”Application for Registration of a Veterinary Medicine” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Registration-of-a-Veterinary-Medicine.pdf”][vc_btn title=”Temporary Guidelines for Hand Sanitizers” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FTemporary-Guidelines-for-Hand-Sanitizers.pdf”][vc_btn title=”Application for Marketing Authorisation – Condoms” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Marketing-Authorisation-Condoms.pdf”][vc_btn title=”Guidelines for Registration of Nutritional Suppliment” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-Registration-of-Nutritional-Suppliment.pdf”][vc_btn title=”Application for Registration a Biological Product” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Registration-a-Biological-Product.pdf”][vc_btn title=”Application for Registration of a Herbal Medicine” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-for-Registration-of-a-Herbal-Medicine.pdf”][vc_btn title=”Checklist for Submission of Dossiers” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FChecklist-for-Submission-of-Dossiers.pdf”][vc_btn title=”Guidelines on submission of applications in CTD Format” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F05%2FZAMRA-Guidelines-on-submission-of-applications-in-CTD-format-_v01-09_04_2015-edited.pdf”][vc_btn title=”Guidelines on Bioavailability or Bioequivalence” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-on-Bioavailability-or-Bioequivalence.pdf”][vc_btn title=”Application for Clincal Trial Authorisation” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F05%2FGuidelines-on-Application-for-Clincal-Trial-Authorisation.pdf”][vc_btn title=”Applicants Cover letter template_v0 – ZAZIBONA” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplicants-Cover-letter-template_v0-ZAZIBONA.pdf”][vc_btn title=”Application acceptance letter – ZAZIBONA” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FApplication-acceptance-letter-ZAZIBONA.pdf”][vc_btn title=”Expression of Interest – ZAZIBONA” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FExpression-of-Interest-ZAZIBONA.pdf”][vc_btn title=”Assessment Process Workflow-v0 – ZAZIBONA” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FAssessment-Process-Workflow-v0-ZAZIBONA.pdf”][vc_btn title=”Roles of key players in Zazibona-process_v0 – ZAZIBONA” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FRoles-of-key-players-in-Zazibona-process_v0-ZAZIBONA.pdf”][vc_btn title=”API FPP Assessment Template-LOQ_v0 – ZAZIBONA” color=”black” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FAPI-FPP-Assessment-Template-LOQ_v0-Zazibona.pdf”][/vc_tta_section][vc_tta_section i_icon_fontawesome=”fas fa-download” add_icon=”true” title=”Licenses and Permits” tab_id=”1679437850166-5f152880-b3a5″][vc_btn title=”Guidelines on the Establishment of a Pharmaceutical Retail Business (Amendment) 2023″ color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F05%2FGuideline-on-Establishment-of-a-Pharmaceutical-Retail-Business-Amendment-2023-1.pdf|target:_blank”][vc_btn title=”Guidelines on the Establishment of a Pharmaceutical Wholesale Business” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-Establishment-of-a-Pharmaceutical-Wholesale-Business-in-Zambia.pdf”][vc_btn title=”Guidelines on the Establishment of a Pharmaceutical Retail Outlet” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-the-Establishment-of-Pharmaceutical-Retail-Business.pdf”][vc_btn title=”Guidelines on the Establishment of an Agro-Veterinary Shop” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGuidelines-for-the-Establishment-of-an-Agro-Veterinary-Shop.pdf”][vc_btn title=”Guidelines on the Establishment of a Health Shop” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F05%2FGUIDELINES-ON-OPERATING-A-HEALTH-SHOPS.pdf”][vc_btn title=”Guidelines on Good Distribution Practices” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.zamra.co.zm%2Fwp-content%2Fuploads%2F2023%2F08%2FGUIDELINES-ON-GOOD-DISTRIBUTION-PRACTICES.pdf”][vc_btn title=”Guidelines on Good Manufacturing Practices (WHO)” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” add_icon=”true” link=”url:https%3A%2F%2Fwww.who.int%2Fteams%2Fhealth-product-and-policy-standards%2Fstandards-and-specifications%2Fnorms-and-standards-for-pharmaceuticals%2Fguidelines%2Fproduction|target:_blank”][vc_btn title=”WHO good manufacturing practices for pharmaceutical products: Main Principles” color=”inverse” i_icon_fontawesome=”far fa-file-pdf” css=”” add_icon=”true” link=”url:https%3A%2F%2Fwww.who.int%2Fpublications%2Fm%2Fitem%2Ftrs986-annex2|target:_blank”][/vc_tta_section][/vc_tta_tabs][/vc_column][vc_column width=”1/6″][/vc_column][/vc_row]