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

Early Bird Price (Valid Till 4th May 2023)) - INR 15,000 + GST (18%) per delegate

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.