Tammy Pillay is a senior regulatory affairs leader with over 20 years of experience in the pharmaceutical industry. She has specialised expertise in international regulatory strategy, CMC quality assurance, pharmacovigilance, clinical trial applications, early access programs, and cross‑functional project leadership.
Tammy has worked across three countries, establishing and scaling regulatory, quality, and safety functions for new affiliates. She has led global submissions, pre‑IND and pre‑NDA interactions, and paediatric clinical trial applications across the EU, USA, and worldwide.
A frequent speaker at universities, NGOs, and international forums, Tammy contributes actively to global regulatory dialogue and has built a strong network across industry, regulators, the WHO, and development partners.