DIA's 8th Annual Conference - The New Clinical Research Environment in India

Join Prominent Professionals to Discuss the Changing Industry Join academia, industry, regulators and researchers to discuss the new environment for health care product development at DIA India’s 8th Annual Conference. The event, to be held in Bangalore from October 24 to 26, will provide a forum for professionals to hear how their peers are coping with the challenges of new regulations and how they are planning to realize the promise of emerging opportunities. More than 90 renowned experts will speak on key issues, including keynote presenters Prof. Ranjit Roychaudhuory, Chairman of the Task Force for Research at Appollo Hospitals Group, and Mukhtar Ahmed, Oracle HSGBU’s Vice President of Product Strategy. The conference will also feature 12 tracks with 48 sessions on the key themes of clinical research, IT, life sciences, medical writing, and biostatistics. Program highlights include: Direction, outlook and vision for health related research in India Review of recent changes in regulations and their implications Challenges to global development and commercialization ex-India New opportunities for India-centric global delivery solutions Global benchmarks in health care research regulations Patient-centric endeavors for awareness and ethics of research Exhibiting and Support Opportunities are available! Click here for more information. Overview View Program Register Now upcoming events THANK YOU TO OUR MEDIA PARTNERS Keynote Speakers Padmashree Ranjit Roy Chaudhury Apollo Hospitals Group Mukhtar Ahmed Oracle HSGBU Featured Topics Drug Discovery Development Manufacturing Commercialization Regulatory Ethical, Social, Legal, Technology & Standards Lean Strategy Outsourcing Strategy Pharmacovigilance Therapeutics Overview View Program Register Now

Email Preferences | My DIA | Forward to a Friend |

Sign up for DIA's Global SmartBrief eNews for the latest in drug development innovations worldwide.

Take part in the Conference on Technological Advances in Meeting Regulatory Challenges - Apr 25 in Mumbai

Nine Days to Go - Register Now! Take part in the Conference on Technological Advances in Meeting Regulatory Challenges and you will have the chance to discuss lean validation concepts and other technological advancements in facility design with regulatory experts and colleagues. The conference, to be held in Mumbai, India on April 25, will be attended by V. G. Somani, deputy drug controller, CDSCO, India and other high-profile participants. Other key topics at the event, which is organized by DIA in collaboration with PharmaPro&Pack Expo, will include ensuring automation in meeting global regulatory challenges and an in-depth view of qualification and validation of facilities, equipment, and utilities.   Overview     Download Program    Register Now Session Highlights Technological Challenges in Meeting Global Regulatory Guidelines Regulatory Views on Qualification/Validation Lean Validation Concepts: ASTM E 2500 ICH Q8/Q9/Q10: Strategy for Successful Implementation Approach to GAMP V Guidelines: Case Studies Regulatory Outcomes: Equipment/Instruments Design Considerations of New Pharma Facilities Containment Technology: Design Challenges Technological Advances in Meeting Regulatory Challenges   Overview     Download Program    Register Now Thank You to Our Event Partner Thank You to Our Media Partner

Sign up for DIA's Global SmartBrief: Break through the information clutter with FREE, twice-weekly email publication that gives quick, easy-to-read summaries of articles relevant to you. Get the latest news in drug development innovations worldwide wherever you are on your laptop or smart phone with SmartBrief’s wireless compatibility.

Show what your company has to offer at 4th Pharmacovigilance Conference in Bangalore

Show what your company has to offer Showcase you company’s product or service and network with industry professionals at the 4th Pharmacovigilance Conference in India. The two-day conference, to be held in Bangalore from March 8-9, brings together pharmacovigilance, clinical research, medical information, and regulatory professionals and academia to discuss the latest global challenges in drug safety. Your company can exhibit with a tabletop display and receive one complimentary full-meeting registration and one exhibit personnel registration. Or become a Platinum Level Supporter and receive three complimentary full-meeting registrations, three exhibit personnel registrations, and exclusive branding and promotion opportunities. Click here for further details and apply today. View Program Download Application Other events of Interest Download the India Calendar of Events Conference Highlights Updates on recently released GPvP Modules by EMA Japanese model of EPPV – a way forward for other Asian countries Challenges in authoring PSUR for generic manufacturers An insight into Drug Induced Liver Injury (DILI) Global regulatory compliance: challenges and the way forward Safety regulations in emerging Middle East region Efficient management of literature searching Enhanced productivity and quality through process re-engineering; case studies Global outsourcing trends in PV – Indian potential and challenges by China, Taiwan, and Latin America RSI management – best practices to safeguard against pitfalls Attrition and manpower stability; KPO perspective Technology-watch against safety hazard of spurious and adulterated drugs Training; A Formality or a Reality – an industry insight Panel discussion: compensation for trial related injuries This Pharmacovigilance Conference is perfect for professionals with experience in clinical safety and who are involved in: Pharmacovigilance Clinical research Risk management Compliance Medical information Regulatory affairs Academia Pharmacology Read More View Program Register To know more, contact Manoj.Trivedi@diaindia.org Thank You to our Media Partner

Email Preferences | My DIA | Forward to a Friend |