What’s the ideal scenario? Of course, the Centre acting as a facilitator, say most experts. Supporting states with financial support, guiding the laggards with a policy grid detailing best practices, becoming a network of shared knowledge, enabling research collaboration, distributing its fruits, becoming a nodal point for learning and teaching at once. But what one saw was the Centre draw on its legal powers to monopolise decision-making on key aspects: testing strategy, drug protocols, suspension of international travel, procurement of emergency supplies, local production of diagnostic kits—things that affected everyone, without anyone being on board. India has invoked the Disaster Management Act (NDMA) 2005 and Epidemic Diseases Act 1897 to do all this, and questions are being asked about the adequacy and validity of the two laws, especially their conflicting provisions. Under Section 2 of the Epidemic Diseases Act—which came into being after the Bombay plague—state governments can adopt exceptional measures to contain a disease. However, under the NDMA Act, the Union health secretary is entrusted with those powers. Says M.R. Madhavan, president, PRS Legislative Research, “NDMA allows centralisation of power, which may not be a good thing during an epidemic. That battle has to be as local as possible.”