Time Research is an independent medical market research agency specialized in conducting research related to international healthcare conferences. They have over 15 years of experience researching over 300 conferences. Their services include quantitative and qualitative research with physicians, patients, journalists, and company staff both at and after conferences. They research all aspects of the conference experience from exhibition stands and messages to sponsored events and speakers. Clients receive tailored reports and fast feedback to help measure return on investment from their conference activities.
Ateneo School of Medicine and Public Health Grading System for the Marketing Management Module designed by Prof. Remigio Joseph De Ungria of the Ateneo Graduate School of Business
Ateneo School of Medicine and Public Health Grading System for the Marketing Management Module designed by Prof. Remigio Joseph De Ungria of the Ateneo Graduate School of Business
BioClinitech- Services And Capabilitiesshravan1198
We are a Medico-Marketing Support Service and Customized IT Solutions Company established
in 2004 and offering innovative products and services to the global pharmaceutical and biotech
industries. Headquartered in Mumbai with a branch office in Hyderabad, the firm was conceived as an attempt to manage the information overload and provide customized and innovative solutions to the global healthcare and allied industries.
The team is a blend of global professionals with wide experience in Healthcare, IT, Biotechnology
and broad training in business and strategy
Our products and services provide clients with the innovative solutions to maximize growth
opportunities and life-cycle of existing products.
Business model includes a comprehensive suite of services designed to impart a global
perspective in two distinct portfolios: IT Solutions - Website Development & Maintenance and
Medico-Marketing Support Services
Affordable Research To Grow Your Hospitals Market SlidesBeth Minnigerode
In today’s ever-changing market, how do you keep a pulse on your patients’ needs? Mary Phelan, senior health care consultant at Standing Partnership, and Lisa Richter, principal at richterintel, will share how market research can help you answer the most burning marketing and communications questions. Learn about a recent hospital case study that will show you how affordable research can help drive your organization’s growth strategy.
Join us to see how research can help elevate the role you play within your organization!
We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications specific to the pharmaceutical industry.
Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
why FDA at my Facility is, and what do I do During an InspectionGlobalCompliancePanel
Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
Medtech.Capabilities.Frost & Sullivan.2009Siddharth Singh
Frost & Sullivan is a growth consulting company. The "Healthcare Practices" focuses on identifying emerging opportunities in Medical Devices industry and offer various market strategies.
A guide to become clinical research associatepptxRidhimaPatel2
An integral part of modules in clinical research courses focus on the ethical standards that have to be implemented without compromising the quality of trial results.
IDMP Implementation - Impact on Data, Systems and Processes. How to cover gap...Torben Haagh
ISO IDMP will be mandatory from July 1st 2016 and it will make a fundamental impact on the way the pharmaceutical industry is required to collect, manage and submit relevant data. Now is the last call for all marketing authorisation holders to (re)think their data submission policies and processes to make sure you close your IDMP implementation gaps in the next 12 month and have a clear vision of the next challenges lying ahead!
Don’t miss out on the opportunity to get your questions answered, to benchmark the stage of your preparation, to initiate partnerships and to take an active part in designing the RIM’s community future agenda! Join us this summer in Berlin and gain valuable, practical information:
# Learn how to assess and analyse data requirements for the IDMP standards by discussing possible interpretations with our expert from regulatory bodies on-site!
# Benchmark your own IDPM Implementation process with peers from both big and mid-size pharma
# Share insights how the IDMP standards are changing the interactions between IT-Systems, company departments, contract manufacturers and regulatory agencies
# Discuss and compare with your peers experiences with vendors and solution providers offering help to achieve your IDMP implementation goals!
For more information visit our website: http://bit.ly/EventWebsite
If you would like to be part of the conference, you can register now here: http://bit.ly/Register-Event
Senior EU Regulatory Operations Specialist Biopharmaceuticals, SwitzerlandAndrew Webb
Our client is an integrated global biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies for the treatment of cancer and inflammatory diseases. It is currently advancing three new blockbuster programs that will help drive revenue to over eight figures by 2017. Over the last five years, it has invested over twice the industry average into R&D.
Provides an overview of our data management and analytics capabilities. Covers areas like internal data management, market research, external market environment assessment, etc.
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BioClinitech- Services And Capabilitiesshravan1198
We are a Medico-Marketing Support Service and Customized IT Solutions Company established
in 2004 and offering innovative products and services to the global pharmaceutical and biotech
industries. Headquartered in Mumbai with a branch office in Hyderabad, the firm was conceived as an attempt to manage the information overload and provide customized and innovative solutions to the global healthcare and allied industries.
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Business model includes a comprehensive suite of services designed to impart a global
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Affordable Research To Grow Your Hospitals Market SlidesBeth Minnigerode
In today’s ever-changing market, how do you keep a pulse on your patients’ needs? Mary Phelan, senior health care consultant at Standing Partnership, and Lisa Richter, principal at richterintel, will share how market research can help you answer the most burning marketing and communications questions. Learn about a recent hospital case study that will show you how affordable research can help drive your organization’s growth strategy.
Join us to see how research can help elevate the role you play within your organization!
We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications specific to the pharmaceutical industry.
Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
why FDA at my Facility is, and what do I do During an InspectionGlobalCompliancePanel
Many regulated companies preparing for FDA inspections are not prepared and the outcome can be negative as we see all the time with enforcement actions. This seminar provides the fundamentals and the ground rules on how to prepare for and survive an FDA inspection no matter if you are a Class I, II, III device or a pharmaceutical or biologics manufacturer.
Medtech.Capabilities.Frost & Sullivan.2009Siddharth Singh
Frost & Sullivan is a growth consulting company. The "Healthcare Practices" focuses on identifying emerging opportunities in Medical Devices industry and offer various market strategies.
A guide to become clinical research associatepptxRidhimaPatel2
An integral part of modules in clinical research courses focus on the ethical standards that have to be implemented without compromising the quality of trial results.
IDMP Implementation - Impact on Data, Systems and Processes. How to cover gap...Torben Haagh
ISO IDMP will be mandatory from July 1st 2016 and it will make a fundamental impact on the way the pharmaceutical industry is required to collect, manage and submit relevant data. Now is the last call for all marketing authorisation holders to (re)think their data submission policies and processes to make sure you close your IDMP implementation gaps in the next 12 month and have a clear vision of the next challenges lying ahead!
Don’t miss out on the opportunity to get your questions answered, to benchmark the stage of your preparation, to initiate partnerships and to take an active part in designing the RIM’s community future agenda! Join us this summer in Berlin and gain valuable, practical information:
# Learn how to assess and analyse data requirements for the IDMP standards by discussing possible interpretations with our expert from regulatory bodies on-site!
# Benchmark your own IDPM Implementation process with peers from both big and mid-size pharma
# Share insights how the IDMP standards are changing the interactions between IT-Systems, company departments, contract manufacturers and regulatory agencies
# Discuss and compare with your peers experiences with vendors and solution providers offering help to achieve your IDMP implementation goals!
For more information visit our website: http://bit.ly/EventWebsite
If you would like to be part of the conference, you can register now here: http://bit.ly/Register-Event
Senior EU Regulatory Operations Specialist Biopharmaceuticals, SwitzerlandAndrew Webb
Our client is an integrated global biopharmaceutical company engaged in the discovery, development and commercialization of novel therapies for the treatment of cancer and inflammatory diseases. It is currently advancing three new blockbuster programs that will help drive revenue to over eight figures by 2017. Over the last five years, it has invested over twice the industry average into R&D.
Provides an overview of our data management and analytics capabilities. Covers areas like internal data management, market research, external market environment assessment, etc.
Similar to Time Research Conference Research Services 2011 (20)
1. Time Research Conference research specialists A guide to our services Unrivalled expertise in all aspects of worldwide healthcare conference delegate research
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9. Time Research process – at conference Doctor visits exhibition at the conference Doctor comes to the independent Time Research stand at the event Doctors / Interviewers use laptop to input responses to your questionnaire Data emailed to Time Research HQ Latest results from the conference are analysed –during or after fieldwork Report produced answering client objectives Client receives actionable insights Topline fast feedback possible
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11. Time Research process – post conference Doctor attends exhibition at conference and returns home Doctor is recruited to conduct your questionnaire online - OR Doctor participates in the interview over the telephone Report produced for client Client receives actionable insights Topline fast feedback possible Time Research obtains conference delegates list or utilises cold calling
12. Market research Conference research touches on many departments in the typical pharma company We help you work with internal departments Clinical Trials KOL Development Business Development Medical Professional Relations Public Relations Conventions Staff Marketing
13. Contact Lorraine Colley Time Research Limited Time House, 56b Crewys Road London NW2 2AD England Tel + 44 (0) 20 8209 2020 Fax + 44 (0) 20 8209 2021 Email [email_address] Website www.timeresearch.co.uk