Mumbai, February 14, 2017: Given all the recent changes in the regulatory environment in the recent past and the regulators’ commitment to a creating a favourable clinical research environment in India, there is now a strong need to rebuild global confidence and trust in doing clinical research in India. This was the unanimous opinion of industry panelists in the concluding session on Does India Feature in Discussions on Global Clinical Study Placements at the 10th Annual ISCR (Indian Society for Clinical Research) Conference. While on one hand, data of global inspections validates the high quality of clinical research being done in India, the clinical research environment is weighed down by negative perceptions of quality and therefore stakeholders need to take a more proactive approach to quality management, they said.
Speaking on the occasion, Ms. Suneela Thatte, President, ISCR said, “It is a key responsibility of each one of us to renew our pledge to quality, patient safety and data integrity and set an example to the rest of the world as to how quality and ethics are not mere tokenism but truly reflect the spirit of the clinical research community in India. When this happens only then will we be able to bridge the gap between India’s potential in the field of clinical research and the actual clinical research being conducted in India at the moment and the gap between perception and reality. We at ISCR would like to reiterate our commitment to continue to engage with all our stakeholder and work towards the creation of a clinical research ecosystem that balances the interests of all stakeholders – particularly the patients.”
Among the highlights of the concluding day was a panel on Research in Rare Diseases which had not for profit organisations, patients, medical and legal professionals talk about the needs of rare disease patients in India and what needs to be done to ensure access to research and early intervention for rare diseases. “Rare diseases are not so rare. If we were to put together the entire population of rare disease patients in the world, it would be the third most populous country,” said Prasanna Shirol, Founder Member, Organisation for Rare Diseases India.
Haemophilia drugs in the country currently meet only 2% of the demand for them said Rupal Panchal a patient of haemophilia while emphasizing the need for access and affordability of drugs to serve the larger population of haemophilia patients in India. Legal expert, Leena Meghaney, said, “It is clear that we need more attention dedicated to rare diseases in developing countries. The EU and U.S. have very clear guidelines in place for these diseases, but developing countries are often so overwhelmed with their disease burden, that they fail to consider the significance of such guidelines.”
Dr Shilpi Bhattacharya, a patient suffering from GNE Myopathy of which there are an estimated 20,000 patients worldwide, talked of how it took the best of medical experts overseas two years to diagnose her illness. “Even today, given the rarity of rare diseases, medical practitioners are more interested in learning about us as ‘case studies’ than as ‘patients’ which makes it very frustrating for us,” she said. The panelists concluded that fast track research and more clinical trials, working more closely with regulators, sharing of knowledge and ethical pricing needed to be high on the agenda of the rare disease community in India.
The panel on Investigator Initiated Research – How Can Investigators Navigate the New Environment for Doing Research in India? addressed the challenges of and solutions to doing more academic research in India. The session highlighted once again the importance of knowledge sharing amongst investigators both on evolving regulations and best practices and the need to ensure a multi-disciplinary approach to investigator-initiated trials through collaboration with industry, global academic institutions, regulators, health economists and policy researchers.
A parallel track was held on medical writing, future directions for medicine and pharma and the various challenges in design, conduct and reporting of clinical data in the country. The final day of the conference also witnessed engaging oral and poster presentations, followed by a prize distribution on these displays.
“The fact that so many of you are at this conference – beating the records of all previous years – is reflective of the optimism and hope the year holds for all of us. The media has also played an important role in building awareness about clinical research and I look forward to their continued support at a critical time when we need to empower patients and the public at large with more information about clinical research that can help them take judicious decisions about their health,” concluded Suneela Thatte.
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