We are thankful to all our Sponsors, Delegates, and Media Partners for their commitment, dedication, and collaboration for the 1st Meridian Clinical Trials. We warmly acknowledge all the Pharmaceutical and Biotechnology companies for putting 1st Meridian Clinical trials in their priority list for first-half 2019 events. Meridian Clinical Trials is an annual conference series for small and midsize pharmaceutical and biotechnology companies mainly from the East Coast. The agenda covers the upcoming and ongoing trends in the clinical trials landscape, it also covers the upcoming challenges the industry is facing and how to tackle them. 2nd Meridian Clinical Trials offers high value networking for Private Companies, Government Regulatory bodies, Research Institutes and Non-profit Organization’s Decision Makers who want to increase their understanding with Clinical Trials.

3rd Meridian Clinical Trials is focused on challenges the small and midsize pharmaceutical and biotechnology companies face while conducting clinical trials. The area of focus remains Clinical Operation, Clinical Development, Outsourcing, Patient-Centric approach, Regulatory, Data management, and using artificial intelligence to conduct clinical trials. The Platform is a combination of Case study Presentations, high interactive Workshops and informative Panel Discussion to maximize interaction between Industry experts and the audience. Our team carefully research and craft the perfect Agenda which fulfills the needs of Clinical Pipelines from start to an end. It provides access to critical Thinking, Best Practices, and Innovations in Clinical Trials Industry.

Nik Tezapsidis
President & CEO
Experienced Chief Executive Officer with a demonstrated history of working in the biotechnology industry.
Ira Spector
CEO
A highly accomplished and results-oriented CLINICAL DEVELOPMENT EXECUTIVE, with a proven record of implementing practical solutions
Mary Potasek
Chief Scientific Officer
Dr. Potasek has a Ph.D. in Biophysics/optical physics with over 20 years of experience in photomedicine. In addition to a significant technical background, she has extensive experience in the industry.
Dr Christophe Tournerie
Owner & CEO
Dr. Tournerie has more than 20 years’ experience in clinical research in Europe and the Asia Pacific, working with biotechnology, pharmaceutical companies, and clinical research organizations.
Stanislav Glezer
Global VP, Medical Affairs
Stan Glezer, MD, MBA is an industry physician, passionate about optimizing the value of pharmaceutical innovation for the patients, through partnering with the healthcare system.
Magdalena Schoeneich
Head of Takeda Digital Accelerator
Magda Schoeneich (Head, Center for Scientific Leadership and Innovation) is an R&D focused organizational innovation expert for Takeda.
Kerensa Saljooqi
Director Clinical Operations
Kerensa Saljooqi Director Clinical Operations at BlackThorn Therapeutics
Mark A. Feitelson
Professor, Molecular, Cellular
In addition to my research projects on hepatitis B and C viruses, I am Chair of the Professional Science Master's Program in Biotechnology at Temple University
Colville Brown, MD
Executive Medical Director
Colville Brown is a healthcare services specialist with several years of experience in the healthcare field.
Eduardo Rodenas
MD Medical Director
Our company was founded in 2008 with a vision of pioneering a potentially new approach to treating patients with cancer and other serious diseases.
Miriam Kidron
Chief Scientific Officer
Dr. Kidron serves as Chief Scientific Officer and Director of Oramed Pharmaceuticals, which she co-founded in 2006.
Eric Walter T. Chojnicki
Takeda Digital Accelerator
As an industry thought leader, Certified PMP and Six Sigma Black Belt I provide strategic vision, CMC expertise and proven success as a program leader of teams responsible for full-cycle operations for therapeutic drug development.

Designing Clinical Trials: Study Protocol Design and Review

Strategies to Identify and Mitigate Risks for First-in-Human & Early Clinical Trials

Developing a Clinical Pipeline: Phase I to phase III

Data Management and Analytics in Clinical Trials.

Artificial Intelligence and Machine Learning In Clinical Development

Choosing the right trial and technology to support entity goals.

Developing an Effective Clinical Outsourcing Strategy; Analyzing Risk and Benefits.

n overview of conducting FDA/EMEA Quality research in APAC

Light-based Clinical Trials in Head and Neck and Non-Small Cell Lung Cancers

Managing risk with contracts: Informed consent, Subject injury, Insurance & Indemnification.

Alzheimer's Clinical Trials: Patient Recruitment, interventions, methodology.

Analyzing and interpreting clinical trials in CNS.

Clinical Trials Monitoring: Qualification, Initiations, Interventions Methodology.

Risk-based monitoring: Site Selection, feasibility, and recruitment.

Patients in Clinical trials: Patient screening and recruitment.

Patient-Centric Framework For Planning and Designing Clinical Trials.

Site less Clinical Trials: The Future of Clinical Trials.

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Event Details
  • Days
    Hours
    Min
    Sec
  • Start Date
    May 11, 2020 09:00
  • End Date
    May 12, 2020 18:00
  • Status
    Upcoming
  • Location
  • Organizer
  • Category
  • Address
    Strada 2a, 20090 Assago MI, Italy
  • Phone
    0674 987 665
  • Fax
    9123 598 453
Sponsors