14th Annual Clinical Trials Summit 2023

                             14th Annual Clinical Trials Summit 2023

                                      “A critical guide for successfully conducting Clinical Trials”

                                23rd – 24th May 2023, Kohinoor Continental Hotel, Mumbai - India

14th Annual Clinical Trials Summit 2023 will provide a platform to discuss on the futuristic advancements in Clinical Trials and clinical research. This multidisciplinary program involves broad participation of people from Clinical Trials community who are focused on learning more about clinical research, Clinical Trials planning & management. This event opens discussion of timely topics of mutual theoretical and practical interest for clinical trial investigators who are developing new drugs and biologics. This groundbreaking platform continues the conversation between business, academics, patient advocacy, and regulatory agencies to discuss new methods and solutions to statistical challenges relevant to the design and analysis of Clinical Trials collaboratively in the real world. It is high time that we look into innovative strategies, new technologies, effective and quality collaborations to address these issues, which can cater to the needs of the patient and the industry.

DELEGATE REGISTRATION:

E-mail - bookings@virtueinsight.com or Call - + 91 44 42108101/+91 9361957193

Standard Price  - (INR 18,000 + GST (18%) per delegate)

SPONSORS:

Principal Partner: Clinical Research Network

Silver Partner: Cognizant SIP, ClinPro Research, Tech Observer, Octalsoft

Exhibitors: Clinevo Technologies, Medclinica, Ancillare, ParadigmIT, CRYO PDP, ClinChoice, Clinion, Neuberg Diagnostics

We have more sponsorship opportunities available for the event, which gives you an opportunity to speak and create brand awareness. 

KEY SPEAKERS:

• GOURI SHANKAR, Assistant Drugs Controller, CDSCO
• PRATIK SHAH, VP - Medical Affairs, Bharat Serums and Vaccines
  
• SADHNA JOGLEKAR, Head, Global Drug Development India, Novartis
• SUYOG MEHTA, VP & Head - Medical Affairs & Clinical Research, India & Emerging Markets, Sun Pharma
• RAHUL GUPTA, Senior Vice President, Regulatory Affairs, USV
  
• SANDESH SAWANT, VP Medical Affairs & Head - Clinical Trials, Cipla
• MANISH SHAH, Associate Vice President, Wockhardt
• YASMIN SHENOY, Director-Regulatory Affairs, Sanofi
• VIPIN SETHI, Asst Vice President, Cadila
• VAIBHAV SALVI, Director and Head – Clinical Study Unit, India and South East Asia, Sanofi
  
• SEEMA PAI, Director Clinical Site Operations – India Cluster, Pfizer
• RISHI JAIN, Director Medical Affairs & Pharmacovigilance, AbbVie
  
• MILIND ANTANI, Leader, Pharma and Healthcare, Nishith Desai Associates
• PRABHAT SINHA, Director Government & Public Affairs, Boehringer Ingelheim
  
• PANKAJ GUPTA, Chief Scientific Officer, Novartis
• SANTOSH TAUR, Director Medical Affairs - Vaccines & Digital, Pfizer
• SHIRAZ KANDAWALLA, Associate Director Regulatory Affairs, Ferring Pharmaceuticals
• LESTTER CRUZ SERRANO, Head of Medical Affairs & Global Site Engagement Lead, Cognizant SIP
• DILIP PAWAR, Director and Head Clinical Development and Medical Affairs, Unichem Laboratories
  
• MUKESH GORI, Associate Director - ESP Management PV Strategy & Operations, Novartis
• QAYUM MUKADDAM, Head of MACR, Tech Observer
• TARANNUM KASHMIRI, Founder and CEO, ClinPro Research
• HITENDRA NATH PANDEY, Associate Director – Statistics, Eli Lilly
• SADANAND KULKARNI, Head- Medical, Regulatory, Vigilance & Quality, Fresenius Kabi
• KEDAR NAYAK, Head - Clinical Development, GSK
• JYOTSNA PATWARDHAN, Cluster Head Clinical / PV Country Quality Middle East / Africa / Turkey / India, Novartis
• KAMLESH PATEL, Head -Medical Affairs & Health Tech, Lupin
• SANKET NEWALE, Head Medical Affairs, Emcure Pharmaceuticals
  
• KAVITA LAMROR, Expert, Real World Investigator & RWD Product Owner, Sanofi
• GANESH KADHE, Country Lead & SLT Member, Scientific & Medical Affairs, Abbott
• ANIKET JOSHI, Associate Global Portfolio Delivery Director, Novartis
• HARSHAD KOTHAWADE, Head of Regulatory Management & Trade Compliance, Merck Group
  
• MAYUR MAYBHATE, Head Medical Affairs, Alkem Laboratories
• VAIBHAV AGARWAL, Head – Digital, Wockhardt
• PRITI THAKOR, Head of Medical Affairs- Southern Asia, Johnson & Johnson
• INDRANIL PURKAIT, General Manager and Head Medical Affairs, Ipca Laboratories
  
• ASHWANI PANDITA, GM Quality Management & Training, Global Clinical Research Operations, Glenmark Pharmaceuticals
• RAJ KHIRASARIA, Regional Medical Operations Champion Specialty Care Africa and Asia, Sanofi
• SEERA DILEEP RAJU, Senior Manager - ML & AI, MSD
• RENUKA NEOGI, CPL Manager, India & SEA Cluster, Sanofi
• VISHWAS SOVANI, Founder Director, Pharmawisdom
• SAKHARAM GARALE, Founder & CEO, RENOVARE Healthcare

Plus more joining soon

KEY THEMES:

• Why Decentralisation is the future of Clinical Trials?
• Challenges and risks for launching decentralized trials
• How to manage a Pandemic/Crisis Management in the Future?
• Lessons from Covid-19 pandemic on conducting global Clinical Trials
• Advantages, challenges, and limitations of technology in Clinical Trials
• Current status, challenges and future outlook of RWE and RWD
• Collaborations between CROs and the Pharmaceutical Industry
• Enhancing Patient centricity and patient safety
• Designing quality into Clinical Trials to optimise patient recruitment
• Impact of digital transformation - Digitizing Clinical Trials
• Data Integrity and Data Management
• Creating Effective Outsourcing Partnerships
• Remote clinical research – Risks and chances
• End-to-end strategic partnership & managing communication gap in CROs
• Are the regulations sufficient in Clinical Trials ? What needs to be done?
• Regulatory updates for bettering Clinical Trials
• Be part of a major networking opportunity

WHO SHOULD ATTEND:

CIOs, CEOs, CDOs, Vice Presidents, Presidents, Heads, Directors and Team Leaders from the following areas: Clinical Research & Development, Clinical Research Services, Clinical Operations, Clinical Data Management, Clinical IT, Clinical Trials , Medical Affairs, Regulatory Affairs, Compliance, Quality control / Assurance/GCP, Clinical Study Design, Safety Surveillance, Subject Recruitment, E-Clinical System

Get more from the event, with a broader scope bringing the whole communications value chain together. Enjoy and make the best out of our dedicated networking time, meet the leading international vendors showcasing the products of tomorrow in the co-located exhibition. Expand your knowledge of the latest business models and strategies in the high-level conference.