Comprehensive Pharmacy Services:
Your Partner in Health and Wellness
SAHPRA regulates and approves medicines, medical devices, and complementary medicines in South Africa. Experts evaluate safety, quality, and compliance before products are licensed for sale. Ongoing monitoring ensures continued safety and efficacy.
SAHPRA’s Quality Assurance (QA) division oversees South Africa’s medicine and medical device manufacturing, testing, and distribution to ensure safety and quality control. They review product validation data and inspect manufacturing facilities to ensure regulatory compliance. The QA division is vital in keeping the South African public safe by ensuring only safe and effective medicines and medical devices are available.
They evaluate, register, and monitor products, as well as detect and manage any issues. SAHPRA is accountable to the South African Minister of Health and operates under the Medicines and Related Substances Act (No.101 of 1965). Their main goal is to ensure the public has access to the best possible healthcare services.
SAHPRA regulates medicines, medical devices, and diagnostic products to ensure they are safe and effective, collaborating with other agencies to promote global healthcare standards. They protect public health by enforcing safety and efficacy standards.
RP Pharma is a pharmaceutical company licensed in terms of Section 22C of the Medicines and Related Substances Act 101 of 1965 and can act as your Applicant or Holder of the Registration Certificate (MA Holder).
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