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  • 16-17 Sept 25 Implementation of a QMS for MD CRM.pdf
  • 2019-08-12_SAAPI-Workshop_RegulatoryWriting.pdf
  • 2019-09-05_SAAPI-Workshop_IT.PDF
  • 2019-10-31_HealthProductsWorkshop.pdf
  • 2019-11-25_DueDiligenceWorkshop.pdf
  • 2020-12-03_DD-n-RIM-Workshop.pdf
  • 2022-08-10_Variations_CourseOutline.pdf
  • 2022-10_SAAPI-Workshop_PI-n-PIL Training.pdf
  • 2022-10_SAAPI-Workshop_PI-n-PIL Training_v2.pdf
  • 2022-12_SAAPI-Workshop_RegulatoryWriting.pdf
  • 2024 SAAPI Conference_Provisional Agenda_V2_11 March 2024.pdf
  • 2024 SAAPI Conference_Provisional Agenda_V3_15 April 2024.pdf
  • 2024 SAAPI Conference_Provisional Agenda_V3_27.03.2024.pdf
  • 2025.02 SAAPI VARIATIONS Workshop Outline.pdf
  • 2026 APRIL SAAPI VARIATIONS Workshop Outline.pdf
  • A PRACTICAL APPROACH IN THE APPLICATION OF NEAR INFRARED SPECTROSCOPY IN THE PHARMACEUTICAL INDUSTRY4548.pdf
  • A practical approach-Compilation of the SmPC and PIL for Generics_course outline (002).pdf
  • A practical approach-Compilation of the SmPC and PIL for Generics_course outline.pdf
  • A-PRACTICAL-APPROACH-IN-THE-APPLICATION-OF-NEAR-INFRARED-SPECTROSCOPY-IN-THE-PHARMACEUTICAL-INDUSTRY4548.pdf
  • Application Portal VLS 30.01.26.pdf
  • Behind the XML Curtain.pdf
  • Biz Writing_Course Outline 07 August 2020_FINAL.pdf
  • Biz Writing_Part 2_Course Outline 12 - 20 October 2020_FINAL.pdf
  • BizWriting_01_SAAPI_2020.pdf
  • Business English Writing.pdf
  • Business Meetings.pdf
  • Business Writing_Part 1_Course Outline_May 2021.pdf
  • Business Writing_Part 2_Course Outline_June 2021.pdf
  • Busting the Myths of eCTD Outline.pdf
  • Call for Event Coordinators SAAPI 2026 Conference.pdf
  • cGMP for SC Personnel from a QA Perspective.pdf
  • cGMP for SC Sept 2025 (2).pdf
  • cGMP for SC Sept 2025.pdf
  • Chaos2Clarity VLS 10.02.26.pdf
  • CleanRoomsHVACGEP_Course Outline.pdf
  • Course Outline - Responsible Pharmacist - Roles and Responsibilities.pdf
  • Course Outline Assessment and Validation of Cold Chain Insulated Contain.pdf
  • Course Outline Assessment and Validation of Cold Chain Insulated Containers Online 27 - 28 October 2020.pdf
  • Course Outline Biologicals_ August 2020.pdf
  • Course Outline Biologics 31 July - 01 August 2019.pdf
  • Course Outline cGMP Principles for Responsible Pharmacists Apr 2024.pdf
  • Course Outline Cold Chain Fundamentals 27 - 28 October 2021.pdf
  • Course Outline Cold Chain Fundamentals Online 17 - 19 June 2019.pdf
  • Course Outline Cold Chain Fundamentals Online 27 - 28 October 2020.pdf
  • Course Outline Dissolution_July 2022.pdf
  • Course Outline Five QMS Elements Apr 2024.pdf
  • Course Outline Medical Device Regulatory Aspects and Documentation 26 September 2019.pdf
  • Course Outline Medical Devices Quality Management Systems.pdf
  • Course Outline QMS Elements 14 15 Sept 2022.pdf
  • Course Outline Validation and Qualification in GDP GWP Environment.pdf
  • Course Outline _Bx Release Review APQR Aug 2026.pdf
  • Course Outline _CAPA CC EC May 2026.pdf
  • Course Outline _Compiling SI schedules and CLs Aug 2025 (1).pdf
  • Course Outline _Deviations_RCA May 2026.pdf
  • Course Outline _Qualification and Validation Requirements 29 Jul 2025.pdf
  • Course Outline _Quality Risk Management Sept 2026.pdf
  • Course Outline _SI and QMR Processes_07Oct2026.pdf
  • Course Outline _Technology Transfer Process and Protocols 22 Jul 2025.pdf
  • Course Outline _Test.pdf
  • Course Outline _Theory_Practical application on 3 QMS Elements Feb 2024.pdf
  • Course Outline-Out-of-Specifications-and-Conducting-Effective-Investigations-18-October-2023.pdf
  • Course Outline-Turning-Quality-by-Design-QbD-into-a-Practical-Reality - 22-23 February 2023.pdf
  • Course Outline-Turning-Quality-by-Design-QbD-into-a-Practical-Reality - 22-23 February 2023395.pdf
  • Course Outline.pdf
  • Course Outline_A Pracical Approach to Technology Transfers 14 - 15 April 2021.pdf
  • Course Outline_Annual cGMP Refresher Training Nov 2024.pdf
  • Course Outline_Annual cGMP Refresher Training Oct 2025 2909.pdf
  • Course Outline_Annual cGMP Refresher Workshop_Oct 2025 (1).pdf
  • Course Outline_Annual cGMP Refresher Workshop_Oct 2025.pdf
  • Course Outline_Annual Product Quality Reviews (APQR).pdf
  • Course Outline_Bioequivalence Final_November 2020.pdf
  • Course Outline_cGMP for Applicant Sites in South Africa (HCR) Oct 2023.pdf
  • Course Outline_cGMP for Management_Oct 2021.pdf
  • Course Outline_cGMP for Pharmaceutical Management Personnel Mar 2024.pdf
  • Course Outline_cGMP Training for Applicant Sites_09 March 2021.pdf
  • Course Outline_Dissolution_06-07 July 2022_FINAL.pdf
  • Course Outline_Dissolution_January 2021.pdf
  • Course Outline_GMP FOR PHARMACEUTICAL WATER SYSTEMS.pdf
  • Course Outline_HCR Management of Technology Transfer_Qualification_Validation processes at CMOs or internal facilitities_ Nov 2023.pdf
  • Course Outline_Inspection Readiness_July 2021.pdf
  • Course Outline_Laboratory Management and GLP_8 February 2022.pdf
  • Course Outline_Labortory Management and GLP.pdf
  • Course Outline_Medical Ethics_SAAPI 2020.pdf
  • Course Outline_Medical Ethics_SAAPI 2020_Updated.pdf
  • Course Outline_PQS for QA Compliance June 2024.pdf
  • Course Outline_QA for QC Laboratory Personnel.pdf
  • Course Outline_Quality Risk Management.pdf
  • Course Outline_Quality Safety and Efficacy of Biosimilars_30-31 August 2022_FINAL.pdf
  • Course Outline_Responsible Pharmacist Roles and Responsibilities_Oct 2022.pdf
  • Course Outline_Responsible Pharmacists Roles and Responsibilities_2026.pdf
  • Course Outline_Responsible Pharmacists Roles and Responsibilities_Aug 2025.pdf
  • Course Outline_Responsible Pharmacists Roles and Responsibilities_Nov 2025.pdf
  • Course Outline_Self_Inspection Auditor Training.pdf
  • Course Outline_WHO_Prequalification_29 July 2021.pdf
  • Course-Outline-cGMP-for-Management-Oct-2021.pdf
  • Course-Outline-cGWP Training-2021.pdf
  • Course-Outline-Cold-Chain-Fundamentals-27-28-October-2021.pdf
  • Course-Outline-Laboratory-Management-and-GLP-8-February-2022.pdf
  • Course-Outline-QMS-Elements-Session-1-and-2-and-3.pdf
  • Course-Outline-Responsible-Pharmacist -Roles-and-Responsibilities-August-2021.pdf
  • Course-Outline-Turning-Quality-by-Design-QbD-into-a-Practical-Reality-08-09-June-2022.pdf
  • Course-Outline-Turning-Quality-by-Design-QbD-into-a-Practical-Reality-23-24-November-2022.pdf
  • Course-Outline-VACCINES-2-Day-Workshop-March 2021.pdf
  • Course-Outline-Validation-for-Medical-Devices-08-10-February-2023.pdf
  • Course-Outline_QUALITY-AUDITING-QUALIFYING-AND-CONDUCTING-SELF-INSPECTIONS.pdf
  • Course_Outline_Assessment_and_Validation_of_Cold_Chain_Insulated_Containers_October_2022.pdf
  • Course_Outline_Cold_Chain_Fundamentals_Online_May_2022.pdf
  • Course_Outline_Quality_Safety_and_Efficacy_of_Biosimilars_30-31_August_2022_FINAL.pdf
  • Course_Outline_RA_Functions_in_Medical_Devices-Role_of_the_SAHPRA_Authorised_Rep_26_May_2022.pdf
  • Course_Outline_System_Validation_in_GDP_GWP_Environment_Fundamentals_October_2022.pdf
  • Course_Outline_System_Validation_in_GDP_GWP_Environment_Fundamentals_September_2022.pdf
  • deputy-responsible-pharmacist-ver2.pdf
  • deputy-responsible-pharmacist.pdf
  • DEVIATION AND CHANGE CONTROL MANAGEMENT DURING ROUTINE_COMMERCIAL MANUFACTURING.pdf
  • Device MD IVD label IFU Symbol UDI and traceability short course 28.07.2026.pdf
  • event-coordinators-saapi-2026-conference.pdf
  • Frank discussion Outline CRM.pdf
  • GAUTHIER LETTER OF INCOME.pdf
  • GMP. guide lines course outline 5th Dec. 2019.pdf
  • Half_Day_Media_Training_Workshop_Programme (002).pdf
  • HANDS.pdf
  • How to write and maintain master document_course outline.pdf
  • How to write and maintain master document_course outline_21 Sep 2021.pdf
  • Implementing a QMS for Health products_3-4 December 2024.pdf
  • Implementing a QMS for Health products_30-31 AUGUST 2023.pdf
  • Implementing a QMS for Health products_30-31 NOVEMBER 2024.pdf
  • Introduction to Ethics Workshop.pdf
  • Introduction to ISO13485 - The 8 clauses May 2021.pdf
  • INTRODUCTION TO ORAL SOLID DOSAGE (OSD) FORMS MANUFACTURING.pdf
  • INTRODUCTION TO ORAL SOLID DOSAGE (OSD) FORMS MANUFACTURING650.pdf
  • INTRODUCTION TO PHARMACEUTICAL DEVELOPMENT - Course Outline Final.pdf
  • INTRODUCTION TO PHARMACEUTICAL DEVELOPMENT Course Outline 07 - 08 July 2021.pdf
  • INTRODUCTION TO PHARMACEUTICAL DEVELOPMENT ONLINE 04 - 07 August 2020.pdf
  • INTRODUCTION TO PHARMACEUTICAL DEVELOPMENT.pdf
  • Introduction to Pharmacovigilance Course Outline 2021.pdf
  • Introduction to Pharmacovigilance in South Africa - 11 July 2019.pdf
  • IntroGMP00_SAAPI 2020.pdf
  • Marketing Code Training 19 June 2019 Course Outline and Registration Form.pdf
  • MCA SAAPI Code Training Webinar 12 Nov 2020.pdf
  • MCA SAAPI Code Training Webinar 19 October 2020.pdf
  • MCA SAAPI Marketing Code 101 Webinar 24 Aug 2021 Invitation Outline.pdf
  • MCA SAAPI - ethical legal product promotion 25th May 2022 invitation and outline.pdf
  • MCA SAAPI Approval of Materials and Events Webinar 27 May 2026 Invitation Outline.pdf
  • MCA SAAPI Approval of Promotional Material and Meetings 18 September 2025 Invitation Outline.pdf
  • MCA SAAPI Code Training Webinar 17 Feb 2021 Invitation.pdf
  • MCA SAAPI Code Training Webinar 19 October 2020.pdf
  • MCA SAAPI Marketing Code 101 Webinar 15th Feb 2023 Invitation Outline.pdf
  • MCA SAAPI Marketing Code 101 Webinar 16 Nov Invitation Outline.pdf
  • MCA SAAPI Marketing Code 101 Webinar 20th July 2022 Invitation Outline.pdf
  • MCA SAAPI Marketing Code 101 Webinar 28th February 2024 Invitation Outline.pdf
  • MCA SAAPI Marketing Code 101 Webinar 5 August 2026 Invitation Outline.pdf
  • MCA SAAPI Marketing Code 101 Webinar 9th March 2022 Invitation Outline.pdf
  • MCA-SAAPI-Marketing-Code-101-Webinar-15th-Feb-2023-Invitation-Outline.pdf
  • MCA-SAAPI-Marketing-Code-101-Webinar-2nd-Nov-2022-Invitation-Outline.pdf
  • MCA-SAAPI-Marketing-Code-Ethical-and-Legal-Product-Promotion-31-May-2023-Invitation-and-Outline.pdf
  • MCA-SAAPI-Webinar-16th-August-2023-Invitation-Outline.pdf
  • MCA-SAAPI-Webinar-16th-August-2023-Invitation-Outline869.pdf
  • MCA-SAAPI-Webinar-Ethical-Legal-8-Nov-2023-Outline-Invitation.pdf
  • MCA.pdf
  • Medical Device post market surveillance and adverse Incident_8-9_May 2024.pdf
  • Medical Device LH AR Mgt Rep conversation.pdf
  • Medical Device Regulatory Aspects and Technical Documentation 21 and 22 July 2021.pdf
  • Medical Device Regulatory Aspects and Technical Documentation 22-23 May 2024.pdf
  • Medical Device Regulatory Aspects and Technical Documentation March 2023 FINAL.pdf
  • Medical Device Regulatory Aspects and Technical Documentation November 2022.pdf
  • Medical-Device-Regulatory-Aspects-and-Technical-Documentation-21-and-22-July-2021.pdf
  • Medical-Device-Regulatory-Aspects-and-Technical-Documentation-March-2023-FINAL.pdf
  • Non conformance Corrective action Preventive action for Medical Devices_short course.pdf
  • Online Training Medical Device Technical Documentation 22 and 23 July 2020.pdf
  • OOS AND CONDUCTING EFFECTIVE INVESTIGATIONS.pdf
  • OUT OF SPECIFICATIONS (OOS) AND CONDUCTING EFFECTIVE INVESTIGATIONS.pdf
  • Outline.pdf
  • Portfolio Manager Bloemfontein.pdf
  • Preliminary Agenda SAAPI 2026 Conference_compressed.pdf
  • PV Symposium_26 November 2020.pdf
  • QMS Auditing Techniques 2-3December2025.pdf
  • QMS vs GMP 4 medicines devices and IVD short course.pdf
  • Qualification and Validation Requirements 09 Sept 2026.pdf
  • Quality Audit Techniques for Health products short course 26.02.26.pdf
  • Quality Audit Techniques for Health products.pdf
  • Quality Audit Techniques for Health products_25-26 March 2025.pdf
  • Quality Audit Techniques for Health products_25-26 OCTOBER 2023 (003).pdf
  • Quality Audit Techniques for Health products_25-26 OCTOBER 2023.pdf
  • Quality Audit Techniques for Health products_30-31 OCTOBER 2024.pdf
  • Quality Management Requirements for Medical Devices 07 and 08 April 2021.pdf
  • Quality Management Requirements for Medical Devices 12 - 13 April 2022.pdf
  • Quality Management Requirements for Medical Devices 18 - 19 July 2023 (002).pdf
  • Quality Management Requirements for Medical Devices short course 24.02.26.pdf
  • Quality Management Requirements for Medical Devices _18-19 July 2023.pdf
  • Quality Management Requirements for Medical Devices _31 july 1 Aug 2024.pdf
  • Quality Management Requirements for Medical Devices.pdf
  • Quality Management Systems AUDITING for Medical Devices 21 - 22 July 2022.pdf
  • quality-assurance-pharmacist.pdf
  • Quality-Management-Requirements-for-Medical-Devices-07-and-08-April-2021.pdf
  • regulatory-assistant-act36.pdf
  • SAAPI 2026 Workshop Outline for Master PQS Documentation.pdf
  • SAAPI 2026 Workshop Outlines_cGWP and cGDP for Licensed Pharmaceutical Facilities_16Apr2026.pdf
  • SAAPI 2026 Workshop Outlines_QA for QC_22and23Apr2026.pdf
  • SAAPI MCA Code Training Webinar 11 May 2021 Invitation and Course Outline.pdf
  • SAAPI PV Symposium Agenda_ 20 September 2023.pdf
  • SAAPI QMS Implement.pdf
  • SAAPI Qualifying and Conducting Self-Inspections Course Outline.pdf
  • SAAPI Quality Auditing_Conducting Contract Acceptor Site Audits Training Course Outline 2022.pdf
  • SAAPI Workshop Outline Green Tick Guaranteed.pdf
  • saapi workshop.pdf
  • SAAPI-Notice-of-27th-Annual-General-Meeting.pdf
  • SAAPI-PO-Invoice-1651.pdf
  • saapi-workshop-cdt-module3.pdf
  • SCAN_20230517_081628906.pdf
  • Strategnos_Workshop Outline.pdf
  • Structure of PQS Curiculum 1.pdf
  • Supplier Management Course Outline_ 19 Aug 2026.pdf
  • System Validation Course Outline R3.pdf
  • Technology Transfer Process for Contract Givers and Contract Acceptors.pdf
  • Training for Pharmaceutical Self Inspection Auditors Jul 2024.pdf
  • TURNING QUALITY BY DESIGN (QbD) INTO A PRACTICAL REALITY.pdf
  • Understanding Risk Management.pdf
  • Validation for Medical Devices_03 - 04 April 2024.pdf
  • Validation for Medical Devices_15-16 Nov 2023.pdf
  • Validation for Medical Devices_short course 29.07.2026.pdf
  • Validation for Medical Devices_short course.pdf
  • Vigilance PMS Conversation for Medical Devices_30.07.2026.pdf
  • Workshop Outline When Change Knocks_Validation.pdf

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• /download/presentation

  • a-redmond-pharma-4-revc-saapi.pdf
  • avanthi-bester-saapi-conference-4-oct-18.pdf
  • candice-sutherland-saapi-cyber-crime.pdf
  • davis-mahlatji.pdf
  • doug-oliver.pdf
  • dr-georg-sindelar-q-oversight-i-saapi.pdf
  • dr-len-konar-integral-pharmaceutical-industry.pdf
  • dr-neil-gower.pdf
  • dr-tienie-stander.pdf
  • enos-motshitela-categories-pharmacists-south-africa.pdf
  • georg-sindelar-q-oversight-ii-saapi.pdf
  • industry-transition-sahpra-dr-joey-gouws.pdf
  • jane-rogers.pdf
  • mr-amos-masango-saapi-conference-2018-update-council-development.pdf
  • mr-dale-gyure-validation-science-practice.pdf
  • ms-anfrea-julsing-keyter-sa-md-update-ar-adverse.pdf
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  • nicola-main-global-regulations.pdf
  • portia-nkambule.pdf
  • prof-helen-rees-sahpra.pdf
  • pual-k-tanui.pdf
  • redmond-data-inegrity-revc-saapi.pdf
  • session-1-global-perspective-health-system- dr-j-lim.pdf
  • session-1-reliance-recognition-dr-luther-gwaza.pdf
  • session-2-professional-standards-mojo-mokoena.pdf
  • session-2-qa-compliance-remediation-john-henchion.pdf
  • session-3-cold-chain-darantis-kosmas.pdf
  • session-3-social-media-mario-botha.pdf
  • session-4-3d-printing-l-du-toit.pdf
  • session-4-facility-future-john-henchion.pdf
  • session-5-cams-practical-approach-wayne-robinson.pdf
  • session-5-sahpra-update-davis-mahlatji.pdf
  • session-6-access-medicines-daphney-fafudi.pdf
  • session-6-medical-devices-avanthi-bester.pdf
  • session-7-cannabis-andy-gray.pdf
  • session-8-cannabis-testing-wayne-robinson.pdf
  • suzette-van-rooyen-mca-saapi-5-oct-2018.pdf
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  • event-coordinators-saapi-2027.pdf
  • proposed-saapi-workshop-2026-ver06.pdf
  • proposed-saapi-workshop.pdf
  • saapi-conference-agenda-june-2026.pdf
  • saapi-conference-provisional-agenda.pdf
  • saapi-constitution.pdf
  • saapi-terms-conditions-workshop-conference-v3.pdf
  • saapi-virtual-congress-2021-final-programme.pdf
  • saapi-workshops.pdf