AMR Innovation Exchange (AMRIX): Zoliflodacin in Thailand - Leveraging Collaboration for Accelerated Regulatory Approval 

Join us in this webinar on a series on innovators, regulators, manufacturers, and clinicians working around the globe on AMR-relevant products and programmes of work. For this webinar we have speaker:

Tammy Pillay, Head of Regulatory Affairs & Quality Assurance Global Antibiotic Research and Development Partnership (GARDP)

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, WHO and development partners. At GARDP, Tammy provides strategic leadership to ensure regulatory compliance and quality governance across GARDP’s R&D activities. She oversees the development, implementation and continuous improvement of regulatory and quality systems to support global product development and access strategies. 

To respect all our delegates privacy we request that you do not take screen grabs, photos or record any of the content, names, people and research during this webinar. We also remind everyone attending our events that some people may may feel uncomfortable with their name, image or research being posted to social media platforms.