• Members and Stakeholder Event

  • Members and non-members welcome

  • Members-only event

  • Members-only event

  • Members-only event

  • Join us for a preview of the presentation that SAMED will make at the upcoming Parliamentary NHI public hearing session. We are striving to inform NHI and linked legislation, including the Public Procurement Bill, and to ensure that the lessons from the pandemic in relation to medtech are part of the discourse and government policy.

    Members-only event

  • SAMED has made some amendments to the Medical Device Code of Ethical Marketing and Business Practice. These changes are aimed at strengthening the Code and providing guidance to our members. Updates include changes to definitions, virtual events and the whistle-blowing hotline processes.

    Members-only event

  • The South African Health Products Regulatory Authority (SAHPRA) has published the amended Draft Medical Device Regulation, Join us as we unpack the challenges, concerns and comments. Come give your views and comments on the impact of these amendments on the medtech sector. Non-members welcome.
  • Digital marketing, communications and HCP interactions that have come to the fore in the pandemic landscape.

    Members-only event

  • B-BBEE fronting in procurement, what it is and how to ensure compliance. The B-BBEE Commission unpacks this practice and the role of consultants to industry.

    Members-only event

  • SAMED is delighted to again partner with Willis Towers Watson (WTW) to research and publish the 2021 Medical Devices Compensation Survey and will be sponsoring the results. The data provided in this survey assist to track the impact of COVID-19 and salary trends. There is no cost to participate in the survey and by providing your Compensation data and HR Policies & Practices and Benefits Design Practices information you will automatically receive complimentary access to the HR Policies & Practices and Benefits Design Practices.

    Members-only event

  • Join us for an overview and interactive discussion on SAMED's submission on the draft Medical Device Regulations. Provide your inputs into the SAMED submission and gain insights for your own submission ahead of the July comment deadline.

    Members-only event

  • The pandemic, new technologies and POPIA; the market landscape has changed and altered the way in which businesses operate. Digital communications and POPIA have altered the medtech market landscape.

    Join us as we unpack digital sales and marketing and how to bridge the gap with Warren Hickenbotham from Blankpage Media and answer your questions on implementing and adhering to the protection of personal information Act with Pat Matseke from Elsabe Klinck and Associates.

    Members-only event

  • While South Africa faces its own medical device regulatory changes, we cannot lose sight of the changes happening abroad. This forum will look at the regulatory developments from across Africa as well as key considerations of the Post-Brexit medical device regulatory landscape for those trading with the UK. Non-members welcome.
  • Earn 2 Ethics CPD points

    In this session learn more about:

    • The requirements and processes for getting CPD accreditation on articles, events and training from MPC Director, Mieder Erasmus
    • Managing requests from HCPs to participate in clinical activities that fall outside of the scope of company representatives, including potential risk and risk mitigation from Vitor Ferrão, Orthopaedic Supplier Committee Vice-chair
    • Developments with SAMED's Section 18A & 18B exemption request on behalf of industry

    Special Guest: Mr Andries Sekgetho, Business Executive at the Auditor General’s Office will provide an overview of their special reports on PPE procurement in the Health sector

    Members-only event

  • Youth unemployment in South Africa has reached a crisis point, 58% of young people are unemployed. As a result, SAMED and YES have embarked on an exciting partnership to unlock work opportunities for SA youth while transforming the country’s medtech and healthcare sectors.

    Learn how, through YES, your business can transform (receiving up to two B-BBEE levels up) while capacitating the healthcare sector. Rethink work. Rethink B-BBEE. Reinvest in our youth for a more resilient and inclusive South Africa.

    Members-only event

  • Long payment timelines are a significant issue that poses a threat to the survival of many companies. SAMED tracks the extent of this problem through the Public Sector Submission Portal and urges members to submit amounts to our portal in order for us to ascertain the extent of delayed payments and to present a unified industry response in an attempt to improve payment timeframes.

    Members-only event

  • Closing date for registration: 8 October 2021

    Members and non-members welcome

    CPD Accredited with 3 Ethics and 9 Clinical CPD Points

  • SAMED Market Access Forum

    In this forum, we take a look at the importance and use of data within medtech market access particularly in reimbursement and procure.

    Members-only event

  • Test

    R0.00R1,000.00
  • In this next forum, we take a look at MedTech Europe's submission on the South African draft Medical Device Regulations and the accreditation requirements for ISO13485.

    • MedTech Europe submission on the SA draft Medical Device Regulations – Diana Kanecka, Senior Manager International Affairs, Medtech Europe
    • Accreditation requirements for the standard ISO13485 - Mookho Morienyane, Assessment Specialist, SANAS

  • Transformation takes strategic intent. This strategic intent needs to have clear goals that will indicate if the strategy is working and the plans to actualise those goals. It takes forethought and leadership with the flexibility to make the most of the opportunities and tenacity to overcome any challenges or setbacks. Join us we discuss transformation as a strategic imperative and an economic opportunity

    Members-only event

  • In this next forum, we take a look at the Medical Device and In Vitro Diagnostic Regulations in Africa and Europe and how this affects the provision of medical technologies in these areas.

    • CSIR Medtech Regulatory support services and programmes  with CSIR Team, led by Jeremy Wallis

    • African Medical Device Regulations - an update with Lizel Dreyer-Fouche, RA Manager: Africa & Middle East, Abbott Molecular

    • Overview of the European MDR and IVDR with Andre ten Napel, Regulatory Consultant, TNMC Medical Devices

  • In this session, we take a look at good ethics: what it is and why it is important with our Special Guest speaker Paul O'Sullivan, Certified Fraud Examiner, Paul O'Sullivan and Associates; the Whistle-Blowing Hotline: Cases, progress and outcomes with our Ethics Chair Michael Judin, Judin Combrink; how to access and interpret Code Compliance Reports from the MPC platform; compliance Officer declaration & re-certification by the end March 2022 deadline; what the latest developments are on the 18A&B exemptions and recognition of the Code; and, some recent Code Advisory Opinions and what you can learn from them

  • 2021/2022: Feedback and forecast Join us as we look back at 2021, our activities and achievements, and the SAMED 2022 vision for a sustainable, ethical and transformed medical technology industry. Mandatory Vaccines: To implement or not? Many health sector organisations have implemented mandatory vaccine policies. Find out why, how, the ethical and legal considerations and what medtech companies should consider before implementing policies of their own.

    Members-only event

  • Calling all medtech executives - be a part of our influential network of business leaders and level up your competitive edge with a BBBEE boost. Join us for our first SAMED CEO Forum as we set the tone and objectives for 2022 and unpack ways to improve sustainability, support industry growth and unlock our sector's transformation potential. You will also hear about the benefits of the Youth Employment Services (YES) programme and how the CSIR have benefited from participation.

    Members-only event

  • Join us for a review of the medtech regulations in Africa. Learn the latest developments in these evolving regulatory frameworks and gain insights into the requirements to trade medical technologies into Africa. Countries to be covered include:

    • Kenya
    • Nigeria
    • Ghana
    • Botswana