Conference - Mumbai, India
• Update yourself with respect to terms of legislation, policies, systems, technology, communication strategies and best practices
• Determining the steps and strategies for enhancing quality in healthcare
• Discovering the new trends in global clinical trials and their role in India
• Technologies that drive efficiencies in global clinical trials
• Strategies to conduct successful interventional oncology trials in India
• Quality by design
• Monitoring, managing and leading clinical trials: An integrated approach for better trial success
• Maintaining proper balance in relationships: Sponsor – Site – CRO & Patients
• Margin of safety: Identifying ideal clinical sites and strategizing patient recruitment and clinical sites management in India to develop appropriate clinical studies
• Effectively incorporating GCP & GCPs – Knowing what TO-DO and what NOT TO-DO
• Re-Thinking patient recruitment and patient experience
• Finding the ideal partner in outsourcing your logistics operations in India how to identify smart packaging solutions to balance quality and costs
• Identifying the decision criteria for partnering with the right vendors in Asia
• How to manage risks in clinical trials effectively and how to successfully incorporate risk sharing models in clinical trials
• Avoiding mistakes in data collection and ensuring profitability and to understand the long term operation strategies for managing clinical trials.
• Overcoming challenges faced in regulatory approval processes – obtaining drug/ clinical supplies import and export licenses in Asia
• Regulatory review at the drugs controller general of India (DCGI) and central drugs standard control organization (CDSCO): science, quality, and speed
• Analyzing the recent government rules and guidelines
• Next generations of clinical trials – How big will the market be?
• Be part of a major networking opportunity
• Determining the steps and strategies for enhancing quality in healthcare
• Discovering the new trends in global clinical trials and their role in India
• Technologies that drive efficiencies in global clinical trials
• Strategies to conduct successful interventional oncology trials in India
• Quality by design
• Monitoring, managing and leading clinical trials: An integrated approach for better trial success
• Maintaining proper balance in relationships: Sponsor – Site – CRO & Patients
• Margin of safety: Identifying ideal clinical sites and strategizing patient recruitment and clinical sites management in India to develop appropriate clinical studies
• Effectively incorporating GCP & GCPs – Knowing what TO-DO and what NOT TO-DO
• Re-Thinking patient recruitment and patient experience
• Finding the ideal partner in outsourcing your logistics operations in India how to identify smart packaging solutions to balance quality and costs
• Identifying the decision criteria for partnering with the right vendors in Asia
• How to manage risks in clinical trials effectively and how to successfully incorporate risk sharing models in clinical trials
• Avoiding mistakes in data collection and ensuring profitability and to understand the long term operation strategies for managing clinical trials.
• Overcoming challenges faced in regulatory approval processes – obtaining drug/ clinical supplies import and export licenses in Asia
• Regulatory review at the drugs controller general of India (DCGI) and central drugs standard control organization (CDSCO): science, quality, and speed
• Analyzing the recent government rules and guidelines
• Next generations of clinical trials – How big will the market be?
• Be part of a major networking opportunity
- Organization: Virtue Insight - Nisha
Thu, May 28, 2015 - Thu, May 28, 2015
Kohinoor Continental Hotel, Mumbai, India
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