Driving South Africa’s pharma and cosmetics forward with science, regulatory clarity, and sustainable innovation.
Grounded in P&C Review’s reporting and standards like CTFA, SAHPRA, IFRA, SCCS, and ISO, we help teams compare ingredients and technologies, build QC and GMP checklists, navigate EPR obligations, and source SA‑first suppliers—so products stay compliant, sustainable, and market‑ready in South Africa.
Meet the P&C team
P&C Review’s all‑female team brings scientific rigor, regulatory clarity, and supplier know‑how to South Africa’s pharma and cosmetics.
Abby Vorster
Editor
Pippa Giesing
Key Account Manager
Andipha Nkoloti
Layout & Design
Mandy Ackerman
Production Controller
Power your SA pharma & cosmetics work with our
free AI assistant.
- Instant, citation‑backed answers for SA formulation, QC/GMP and regs.
- SA‑first supplier shortlists, RFQs and transparent sponsor options.
- Export checklists and briefs, plus alerts for IFRA, SAHPRA and EPR.
FAQs
What is P&C Review and who do you serve?
P&C Review is a South Africa–focused, all‑female–led editorial brand that equips pharmaceutical and cosmetics professionals — formulators, QA/QC, regulatory, packaging, procurement, fragrance, and leaders with reference‑grade insights on formulation, compliance, sustainability, and supplier intelligence across SA and Sub‑Saharan Africa.
How do you help with sourcing and partnerships?
Our reporting is grounded in standards and regulators such as CTFA, SAHPRA, IFRA, SCCS/EU, REACH, ISO 22716/16128, and EPR frameworks, with clear citations and South African context; sponsor content is transparently labeled, and editorial independence guides our coverage.
What regions do you focus on?
Our primary focus is South Africa with Sub‑Saharan coverage; we add EU/US crosswalks when risk or requirements differ or when readers request them.
What is the AI on P&C Review and how can it help me?
Our AI companion delivers concise, citation‑backed answers, IFRA‑aware fragrance guidance, QC/GMP checklists, EPR packaging pointers, and SA‑centric regulatory summaries; it can draft RFQs and export DOCX briefs, defaults to South African rules, and includes a safety disclaimer (information only; verify latest standards).
How are corrections and clarifications handled?
If something needs revision, we correct promptly, note the update, and, when applicable, provide links to the governing standard or regulator for verification.