Entrepreneurial pharmacist’s women-powered business ready to soar
Drickus Maartens • August 7, 2020
Phumeza Langalibalele, owner of Mlungisi Healthcare, says that her business employs only women and looks for opportunities to develop raw talent wherever possible. Langalibalele (left) is pictured with Anda Buka, senior administrator at Mlungisi Healthcare.
Growing women and inclusivity in SA’s healthcare supply chains
Ever since she was studying to be a pharmacist, Phumeza Langalibalele dreamt of launching her own healthcare enterprise. Years of studying, hard work, and difficult decisions along the way to realise her dream of starting up a healthcare supplies business, are now reaching fruition for Langalibalele’s brainchild, Mlungisi Healthcare, thanks to a supportive corporate.
“The vision when I registered the company in 2011 was to start a local business manufacturing pharmaceuticals but I came to realise that the barriers to entry were too high, even for someone who has always been restless to achieve success. I therefore decided to start a supplier business instead, and this turned out to be a blessing in disguise,” she says.
Langalibalele, who qualified as a pharmacist before embarking on business management studies including completion of a Management Development Programme (MDP) and a Master of Business Leadership programme, resigned from a high-powered job and worked on a contract basis to secure an income while she set the wheels in motion to launch Mlungisi Healthcare, which started operating in 2015.
“I employed two women at first, and we struggled financially for 13 months before we secured our first contract. Even when more orders came in, as a start-up business with limited capital, we battled to finance the volumes we needed to compete with the bigger, more established suppliers of surgical consumables,” Langalibalele recalls.
“I put everything I had into the business, matching and even exceeding the levels of service that our multinational competitors could offer. However, the capital I needed to meet our obligations on a scale that would enable the business to grow and compete on a more level playing field still remained a major stumbling block.”
In 2016, as part of Netcare’s strategy to drive greater inclusivity in its own healthcare supply chains, the private healthcare group began discussions with Mlungisi Healthcare, a 100% black women-owned small business, adds Dr Nceba Ndzwayiba, director: transformation of Netcare.
“We immediately recognised that, with a little incubation and mentorship, Mlungisi Healthcare had the potential to grow and become a competitive player in the supply of surgical gloves and related consumables.”
Netcare started purchasing surgical consumables from Mlungisi Healthcare, and in 2018 granted the fledgling business a bridging loan of R20 million that would enable them to purchase stock in greater quantities to fulfil larger contracts.
Langalibalele says: “Netcare made it possible for us, with very favourable conditions, to acquire the stock we needed. This enabled us to sell not only to the Netcare Group and the public health sector, but to other private healthcare providers as well. From there, it has been a steep learning curve but our business has taken flight.”
According to Dr Ndzwayiba, Netcare’s enterprise and supplier development (ESD) partnership with Mlungisi Healthcare included exposure to experts who specialise in the import of surgical consumables, negotiations with the distributing company, and guaranteed access to the Netcare market as a sole supplier for surgical gloves, suction liners and canisters for all Netcare hospitals across the country. The business also received assistance with formalising its financial management and accounting systems, which are a crucial foundation for growth.
“At one stage, Phumeza presented her projected growth for the business and we suggested that the forecast was too optimistic, but she amazed us all however, and Mlungisi Healthcare managed to achieve the growth which she had set her sights on.
“We helped Phumeza to enrol on an enterprise accelerator programme to attain the necessary knowledge and skills to develop her business acumen rapidly to match the pace of her company’s growth. We are delighted that Mlungisi Healthcare is fast reaching the point of graduating from its incubation period towards growing its operations sustainably and independently.”
In addition to the productive value of small, medium and micro enterprises (SMMEs) and their direct contribution to socio-economic development in South Africa, Mlungisi Healthcare is also creating opportunities that empower women and contributing towards improving gender equality in the workplace.
“We only employ women, and I am passionate about making a difference in the lives of persons working at Mlungisi Healthcare,” Langalibalele says. “Wherever possible, for each formally qualified woman we recruit, we try to also employ an unskilled person who is interested and eager to learn. This provides immensely valuable practical experience and opportunities which foster the personal growth of these individuals, while also growing the skills base within our company.
“When the person is trained and has shown their affinity, it is not surprising that they are sometimes ‘poached’ for the skills they developed at Mlungisi Healthcare, and in fact this fills me with joy.”
Mlungisi Healthcare has refined its operations through the use of digital technology, and diversified its product range, including the expansion of its personal protective equipment (PPE) range and other products which are much needed in this time of fighting the COVID-19 pandemic.
“The value of the relationships we have built with our manufacturers, suppliers and the companies which buy from us, particularly Netcare, is immeasurable. The increasing scale of the orders we are placing as our business grows has demonstrated the local demand for certain products. One international manufacturer has expressed interest in the possibility of opening a factory here in South Africa, which would be a wonderful opportunity to create jobs for South Africans,” explains Langalibalele.
Dr Ndzwayiba adds: “Langalibalele and Mlungisi Healthcare have achieved remarkable progress so far. It is humbling to partner with an SMME that has made the most of every opportunity to equip itself for sustainable growth, while in turn making a contribution to developing individual women. With a mentor like Phumeza, I have no doubt that these women will make their mark too.
“As a responsible South African corporate citizen, Netcare
is committed to supporting the economic inclusion of black owned and black women-owned enterprises in its supply chain; and we have significantly increased our procurement spend on these supplier categories in recent years to over R4 billion for majority black owned enterprises and R2 billion for black women owned enterprises, and these meet and exceed the targets set out in the B-BBEE codes.
“Over and above our core business of providing the best and safest care, Netcare’s transformative initiatives help in the building of small businesses, which are the lifeblood of our communities and our country’s economy,” he concluded.

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The lives of millions of South Africans with a litany of rare diseases can be vastly improved, and even saved, by addressing challenges in identifying, studying and treating their conditions. With Rare Disease Day on the 28th of February 2025, the Rare Diseases Access Initiative (RDAI) is driving an evolution of the country’s healthcare, through innovative strategies to better care for over 4.2million people living with an estimated 7000 rare diseases. “As our healthcare system faces significant changes in the years ahead, it is vital that we also advocate for people living with rare diseases in South Africa, especially those with limited healthcare access,” said Kelly du Plessis, CEO of Rare Diseases South Africa (RDSA), a member of RDAI. “As part of our ongoing research and awareness efforts, RDAI has conducted an initial analysis of the incidence and prevalence of rare diseases within the country.” This research will assist in improving access to healthcare, policy development, and patient advocacy, while giving critical insight into the challenges faced by patients. “According to research, some rare diseases affect fewer than 1 in a million people, while others, such as Down syndrome, cystic fibrosis, and haemophilia, have a more recognisable prevalence,” says Dr. Helen Malherbe, RDAI lead researcher on rare disease prevalence data. “Many conditions are undetected, underdiagnosed or misdiagnosed, with too many having no information available about them at all.” The RDAI was formed in 2019 to promote a more favourable environment for those impacted by rare diseases in South Africa. Participants include Ampath, the Board of Healthcare Funders (BHF), Discovery Health, Genetic Counsellors South Africa (SASHG), the Government Employees Medical Scheme (GEMS), Health Funders Association (HFA), Medihelp, Medscheme, North-West University (NWU), Rare Diseases South Africa (RDSA), the South African Medical Association (SAMA) and The South African Medical Technology Industry Association (SAMED). The Council for Medical Schemes (CMS) participates as an observer. In the same year, Rare Disease International signed a memorandum of understanding with the World Health Organisation leading to an international rare disease policy framework. In 2021, the United Nations General Assembly moved to adopt a resolution recognising 300 million people living with rare diseases worldwide. “A general lack of awareness and delayed diagnosis remain major hurdles for those affected by rare diseases. Policymakers and healthcare stakeholders need to prioritise access to treatment, diagnosis, and support for rare disease patients,” says Bada Pharasi, CEO of IPASA, “Through this initiative, working collaboratively with stakeholders at every level of the healthcare supply chain, we can bring real and meaningful change to those affected, including family members and care givers, through smart and efficient strategies.” The globally agreed definition of a rare disease is any medical condition with a specific pattern of clinical signs, symptoms, and findings that affects fewer than or equal to 1 in 2000 persons in a population. “Most are genetic, and some are inherited and passed down in families,” Malherbe says. “Some affect only the patient’s genetic recipe, while others may be acquired during life due to infection, trauma, or environmental effects. For many, the cause is still unknown. “These conditions mainly affect children, as they are largely incurable and many are life-threatening. Some require specialised and co-ordinated care, some have limited and expensive treatment options, while others have no information or effective treatments at all,” she adds. The RDAI is calling for a patient-centred care model built on equitable access, transparency and efficiency. Naturally, this model calls for the open participation of patients, the healthcare industry, health professionals, and the Government. “The most critical elements are robust diagnosis standards, improved access to treatment, data collection and management, co-ordination of care, measurement of outcomes and ongoing collaborative research,” du Plessis says. “We need to establish rare disease advisory committees, map gaps and opportunities, establish system requirements, create a roadmap and plan a phased implementation with clear timelines.” The RDAI states that these policy development steps would be a start in quantifying the disease burden and defining standards of care. This would be followed by building and strengthening the capacity to facilitate appropriate diagnosis, treatment, continuity and data monitoring. Thoneshan Naidoo, Chief Executive Officer of the Health Funders Association noted that, “We appreciate the unique opportunity provided by RDAI which enables stakeholders across the industry to work together and identify strategies that improve equitable access to the appropriate diagnosis, treatment and healthcare services for rare disease patients, in an affordable and sustainable manner, taking account of the other pressing needs across the healthcare system.” “True innovation in healthcare is only possible through partnerships and joint advocacy efforts that raise awareness and improve access to treatment. Our long-term goal is the development of a rare diseases policy framework and guidelines for coordinated care,” says Pharasi. “Our members are united in the commitment to unlocking improved patient outcomes and improving access to services and robust health needs assessment facilities.” he concludes. About RDAI The Rare Diseases Access Initiative (RDAI) is dedicated to advocating for improved healthcare access, policy development, and patient support for those affected by rare diseases in South Africa. The initiative brings together key healthcare stakeholders, including pharmaceutical associations, funders, genetic specialists, and patient advocacy groups, to drive impactful change. About RDSA Founded in 2013, Rare Diseases South Africa (RDSA) is a non-profit organisation advocating to ensure that people living with rare diseases and congenital disorders experience greater recognition, support, improved health service and better overall quality of life. Started out of personal need following the diagnosis of organisation founder, Kelly du Plessis' son, it became evident that there was a lack of awareness and support for rare diseases in general in South Africa. About IPASA The Innovative Pharmaceutical Association South Africa (IPASA) is a voluntary trade association representing 24 leading pharmaceutical companies committed to research, development, and innovation. Our mission is to drive healthcare advancement by advocating for policies that improve patient access to safe, high-quality, and affordable medicines.