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Emerging Market Webinars - Archived

Emerging markets are an exciting new area of development in the clinical trials space. Traditionally, North America and Western Europe have been the engine for research. Now, emerging markets involve clinical trials include centres based in Asia, Central and Eastern Europe, Central and South America and the Middle East. The emerging market webinars listed here are recordings of past events. Simply register, for free, for any webinar by clicking the download archive button on each webinar page. If “emerging markets” is to broad a term, don’t forget, you can search our webinar catalog using the search bar, or, if you’re looking for something else, browse through our other topics.

  Synopsis Webinar Title Date

LifeSciences - This webinar help viewers understand the surprising ways on how local sourcing can offer unique benefits to your clinical program
Speaker: Jason Nolte, Comparator Key Account Manager, Fisher Clinical Services
Local Sourcing for Clinical Trials – Overview and Challenges Dec 3, 2015

 

LifeSciences - The speaker will share her perspective and suggest best practice initiatives on how to achieve success in clinical research in this region
Speaker: Mathilde (Tilly) Niessen, Distribution Project Manager, Fisher Clinical Services
Clinical Trials – Russia & Ukraine – Opportunities and Challenges Sept 15, 2015

 

LifeSciences - This presentation on the new EU clinical trials regulation will identify what’s happening with the regulation that governs clinical trials in Europe
Speaker: Dr. Martine Dehlinger-Kremer, Global VP, Medical and Regulatory Affairs, SynteractHCR
The New EU Clinical Trials Regulation: What You Need to Know Before 2016 Jul 23, 2015
LifeSciences - In this webinar, the speakers will clearly defining eSource and consider its potential benefits, DATATRAK
Speakers: Dr. Bill Gluck, Vice President Clinical Knowledge
Tim Lyons, Vice President, Product Development and Operations, DATATRAK
eSource Data Capture Simplified — Uncover Time and Cost Saving Possibilities May 15, 2015
Quintiles experts will discuss practices that will help emerging biopharma companies design smarter trials to put their products on a more predictable path to success
Speakers: Seth Berry, PharmD, Director, Clinical Pharmacokinetic / Pharmacodynamic Modeling & Simulation, Quintiles
Laura Marquis, Vice President and Global Head, Emerging Biopharma, Quintiles
Cara Willoughby, Senior Director, Infosario Design Delivery Lead, Quintiles
Emerging Biopharma: Designing Smarter, More Predictable Clinical Trials Mar 25, 2015
Discussion of the current clinical trial regulatory scenario in India and the many aspects involved in conducting clinical trials in this region
Speaker: Dr. Renu Razdan, Chief Operating Officer, Max Neeman International
Clinical Trials in India: Approval Process Sep 26/14
During this webinar, the presenter will discuss the opportunities and challenges and provide tips on how to achieve success in running clinical trials in China
Speaker: Ianne Loh, General Manager, Fisher Clinical Services, China
China – Land of Opportunities & Challenges for the Clinical Research Industry Sep 10/14
Join ACM Global Central Lab and Pharm-Olam to learn the key considerations in working with outsourced partners in minimizing study start-up times, processing times and in optimizing work efficiencies
Speakers: Mark Engelhart, Chief Commercial Officer, ACM Global Central Laboratory
Jerry Boxall, Managing Director, ACM Europe and Asia ACM Global Central Laboratory
Dr. Yamin “Mo” Khan, Executive VP of Global Clinical Development Pharm-Olam International
Successful Management of Global Studies in Emerging Markets – Key Considerations from the CRO and Central Laboratory Perspective Jun 30/14
This webinar will address in more detail the advantages of globalization as well as the best practices for overcoming the challenges
Speakers: Garth Tierney, Executive Vice President, Asia/Pacific, INC Research
Silvia Zieher, President, Clinical Development and Latin America Operations, INC Research
Globalizing Clinical Trials to Include Emerging Markets Nov 12/13
In this webinar, an overview of the market environment along with the key operational, logistical, and regulatory aspects of conducting clinical trials in China and other Asian countries will be discussed
Speakers: Li Yan, MD, PhD, Executive Director of Clinical Development for Infectious Diseases, Oncology, Respiratory & Immunology, and Vaccines in Emerging Markets, Merck
Patrice Hugo, PhD, Chief Scientist, LabCorp Clinical Trials
Current Trends for Conducting Clinical Trials in China Nov 12/13
This second webinar in the series will examine market access related issues in Japan, South Korea and Taiwan including the ongoing healthcare reform and its implication on access
Speaker: Chia Wen Lee, Head of Emerging Markets Access, Biogen Idec

Evolving Market Access in the APAC Region: The Pharmaceutical Market in Japan, South Korea and Taiwan

Sep 6/13

A discussion of platforms, platform selection and migration, optimising tests for FFPE tissue, clinical delivery for trial enrichment, and development routes for companion diagnostics
Speaker: Dr. Austin Tanney, Scientific Liaison Manager, Almac
Optimizing Assays from FFPE for Biomarker Strategies Sep 4/13
This presentation will examine recent changes in Indian clinical trial regulations, iImmediate and long term impacts, an foreseeable opportunities
Speaker: Dr. Josemund Menezes, MBBS, Regional Director, Clinical Development (Asia-Pacific), Sanofi Pasteur

Adhering Navigating the Dynamic Indian Clinical Trial Landscape

Jun 28/13

This webinar will provide an overview of clinical outsourcing in the MENA (Middle East and North Africa) and APAC (Asia-Pacific) regions and will provide considerations for programs of development
Speaker: Larry Ajuwon, (former) Senior Outsourcing Manager, Genzyme Europe, the Netherlands

Clinical Development, Contracts and Outsourcing in MENA & APAC

Jun 19/13

A discussion of the clinical research scenario in S.E. Asia including market opportunity, registration, new regulatory and safety guidelines
Speakers: Dr. Shariq Anwar, Head of Operations, Max Neeman International
Donald Swankie, MBA, Vice President, USA, Max Neeman International
S.E. Asia Drug/Device Update: Market Potential and Regulatory Environment Jun 6/13
This first webinar in the series will examine market access related issues in China, including the ongoing healthcare reform in China and its implication on access
Speaker: Chia Wen Lee, Head of Emerging Markets Access, Biogen Idec

Evolving Market Access in the APAC Region: The Pharmaceutical Market in China

Apr 18/13

LifeSciences This fourth webinar in our series will focus on the regulatory aspects of conducting clinical trials in Russia
Speakers: Yuri Afonchikov, MD, PhD, Vice President, Regulatory Affairs, Synergy Research Group
Igor Stefanov, Director, General Manager, Synergy Research Group
WEBINAR SERIES: Conducting Clinical Trials in Emerging Markets
Part 4 - Regulatory Affairs: The Key to Russia
Apr 10/13
LifeSciences The speakers will evaluate the quality of clinical trials being conducted in Russia / Ukraine compared to Western Europe, Eastern Europe and other Emerging Markets based on the results of recent FDA inspections conducted at clinical trial sites in these regions
Speakers: David Passov, MBA Senior Vice President, Eastern Europe, ClinStar, A PRA Company
Stanislav Gneushev, MD, MRQA, Director, Quality Assurance, ClinStar, A PRA Company
An Evaluation of Clinical Trial Quality in Russia / Ukraine Compared to Western Europe, Eastern Europe and Other Emerging Markets Mar 22/13
LifeSciences This third webinar in our series will focus on how conducting clinical trials in Russia can help cut the cost of clinical research
Speakers: Sergei Varshavsky, MD, PhD, Sr. VP, Global Strategy, Synergy Research Group
Igor Stefanov, Director, General Manager, Synergy Research Group
WEBINAR SERIES: Conducting Clinical Trials in Emerging Markets
Part 3 - Cutting the Cost of Clinical Research: The Solution Comes from Russia
Feb 25/13
This webinar will focus on ensuring compliance with international and local country specific PV Requirements from an Asia-Pacific perspective
Speaker: Michal Borawski, International Pharmacovigilance Officer for the Asia-Pacific Region Affairs, Sanofi Pasteur

How to Ensure Pharmacovigilance Practices are Compliant with Global Safety Requirements: Challenges in Asia-Pacific

Jan 30/13

In this presentation, a detailed description of the requirements for registration and post-marketing, as well as a Pharmacovigilance plan will be discussed
Speaker: Vijay Tammara, VP Global Regulatory Affairs, Nuron Biotech, AAPS Member

Biosimilar Regulatory Guidelines in Emerging Markets – India

Jan 24/13

LifeSciences This second webinar in the series will examine the the advantages and disadvantages of conducting clinical trials in Russia and Kazakhstan, and the upcoming trends in this market
Speakers: Igor Stefanov, Director, General Manager, Synergy Research Group
Anna Ravdel, Director of Business Development, Synergy Research Group
Evgeny (Eugene) Rogov, MD, PhD, JD, Deputy Head of Clinical Trials State Control Department (ROSZDRAVNADZOR)
WEBINAR SERIES: Conducting Clinical Trials in Emerging Markets
Part 2 - Conducting Cinical Trials in Russia and Kazakhstan
Oct 12/12
LifeSciences An examination of why Asia-Pac excels as a region for strategic clinical data management / medical writing base in which to achieve savings in cost and time investment
Speakers: Koteshwar Govind, Head of Data Management, Max Neeman International
Donald Swankie, MBA, Vice President, USA, Max Neeman International
Global Data Management & Medical Writing: The Asia-Pac Advantage

Sep 26/12

LifeSciences The presentation give an overview of the advantages of conducting clinical trials in emerging markets, an analysis of the importance of start-up timelines in the decision-making process when selecting geographies for a global clinical trial, and a review of the regulatory challenges that can be anticipated when starting up a trial in Russia
Speakers: Leon Dzivinsky, Senior Vice President & General Counsel, ClinStar, LLC / IMP Logistics
Richard Koenig, Vice President of Operations, ClinStar
Study Start-up: A Comparison Across Emerging Markets Sep 13/12
BusinessStrategy This program will analyze the basis of India’s Regulatory environment, the regulations [both current and future] of clinical trials in India, and the challenges faced in the present scenario
Speakers from Max Neeman International: Renu Razdan, PhD, Chief Operating Officer
Vandana Pandey, Manager Regulatory Affairs
Clinical Research in India – Regulatory Environment May 9/12
BusinessStrategy This program will analyze the basis of India’s Regulatory environment, the regulations [both current and future] of clinical trials in India, and the challenges faced in the present scenario
Speakers from Max Neeman International: Renu Razdan, PhD, Chief Operating Officer
Vandana Pandey, Manager Regulatory Affairs
Donald Swankie, MBA, Vice President, USA
Asia-Pac Clinical Research – Regulatory Environment Mar 28/12
LifeSciences This first webinar in the series will examine the the advantages and disadvantages of conducting clinical trials in Russia, the clinical studies cycle, regulatory environment, and impact of the new Drug Law in Russia on the clinical trials
Speakers: Igor Stefanov, Director, General Manager, Synergy Research Group
Anna Ravdel, Director of Business Development, Synergy Research Group
Evgeny (Eugene) Rogov, MD, PhD, JD, Deputy Head of Clinical Trials State Control Department (ROSZDRAVNADZOR)
WEBINAR SERIES: Conducting Clinical Trials in Emerging Markets
Part 1 - Russia: Understanding the Regulatory Environment, Challenges & Benefits
Mar 13/12
LifeSciences This program will provide an overview and key lessons in leveraging India as a strategic venue for research as well as post market approval in a country of 1.3 Billion
Speaker panel from Max Neeman International: Ajoy Kumar, MD, CEO, Renu Razdan, COO, and Donald Swankie, MBA, VP, USA
Clinical Research in India – Potential & Challenges Jun 15/11

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