Tagged pharmacovigilance
Press Release
Recent Technological Advancements in Medical Communication, New Webinar Hosted by Xtalks
Join this webinar for a discussion of the most common medical communications business challenges and potential solutions. This event will also feature a live demonstration of how patient-centric medical communications technology can be leveraged to streamline and optimize medical inquiry fulfillment, adverse event reporting and product complaint management. Read More
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Crossing the Blood-Brain Barrier - the Human Element of Abuse Potential Assessment, New Webinar Hosted by Xtalks
CNS drug developers have to focus on physical safety and efficacy first, especially when developing products for rare disorders or diagnoses that are often unresponsive to other therapies. Although these products rarely have notable CNS mediated side effects, they fall under the FDA's requirement for an abuse potential assessment because they cross the blood-brain barrier. Read More
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An Automated Approach to Global Adverse Event Reporting in Pharmacovigilance, New Webinar Hosted by Xtalks
Session will help practitioners understand the benefits of using the tool and how organizations can proactively manage receipt acknowledgements, oversee distribution from a user-friendly dashboard and increase overall compliance in a cost-effective way through automation Read More
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An NGS Approach for Research on the Genetic Determinants of Female and Male Infertility, New Webinar Hosted by Xtalks
Comprehensive Interrogation of the Genetic Determinants of Female and Male Infertility: A New NGS Research Application Enabled by Improvements in Target Enrichment Technology Read More
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Real World Evidence: A Data-Centric Approach to Efficiently and Securely Drive Value for the Future of Pharma, New Webinar Hosted by Xtalks
Presenters discuss how clinical innovators, Market Access, IT and HEOR can accelerate RWE initiatives and the implications for data security and healthcare decision-making Read More
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ОСТ Incorporates the CORE Reference Project Developed by the European and American Medical Writers Associations
At the Munich conference, which took place in May 2016, the European Medical Writers Association (EMWA) announced the publication of the final version of the CORE Reference (Clarity and Openness in Reporting: E3-based) recommendations, which were developed together with the American Medical Writers Association (AMWA). Read More
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4C Pharma Attends the 6th Annual Pharmacovigilance & Risk Management Strategies Forum Munich
The 6th Annual Pharmacovigilance & Risk Management Strategies 2016 brings together Pharmacovigilance and Drug Safety Officers, EU and National Regulatory, Clinical Risk-Benefit Groups, Regulatory Affairs Officers, Consultancies, Local Medicines Authorities, CROs and others. Read More
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Stottler Henke Releases Enhanced Version of DataMontage Data Visualization Software
Stottler Henke Associates, Inc. today announced the immediate availability of an enhanced version of its DataMontage™ software for rapid visual analysis of complex, time-oriented data. DataMontage 4.0 introduces dozens of new features that enable analysts to visualize data more flexibly and interactively. Read More
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Synowledge Observes Rare Disease Day
Synowledge is a global provider of drug safety, regulatory affairs and related IT solutions to small, mid and large sized pharmaceutical and biotechnology companies. Our comprehensive outsourcing solutions combine the unique strengths of both onshore Read More
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BioPharm Systems to Host Webinar on Using Oracle Health Sciences Empirica Topics to Document Your Signal Management Process
Leading provider of Oracle's clinical trial, data, and dug safety software will discuss why and how Empirica Topics should be implemented and used to strengthen an organization's pharmacovigilance systems and processes. Read More
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Medical Research and GCP Training Services in Russia
UK based MNC,Helix Research Center has announced Medical Research and GCP Training Services for the Global Biopharmaceutical,Medical Device,Cosmetic companies and other R&D Promoters willing to conduct their Clinical Trials in Russia Read More
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GCP Compliance &Clinical Trial Subject Protection Program for Global Healthcare Industry
UK based MNC,Helix Research Center has announced 'GCP Compliance and Clinical Trial Subject Protection Program' for the Researchers and Healthcare Providers in North America,South America,Asia,Africa,Oceania and Europe Read More
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Professional Services for the R&D Stakeholders Worldwide
The Clinical Research Services Division of UK based MNC,Helix Research Center Ltd has announced,'Professional Services ' for the R&D Stakeholders outsourcing their Clinical Research and Training Projects to CROs Worldwide. Read More
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Clinical Research and ICH GCP Training Services in Japan
UK based MNC,Helix Research Center Ltd has announced Clinical Research and ICH GCP Training Services for the Global Biopharmaceutical,Medical Device and Cosmetic Industry and Global Voluntary Organisations Promoting R&D Services in Japan Read More
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Practical Training on Clinical Data Management ,SAS and pharmacovigilance at Mokshabio,hyd
Moksha Biosciences is a Hyderabad Based Contract Research Organization to Support Global and Indian Pharmaceutical and Biotech companies in their Preclinical, Bio analytical and Clinical Development programs. Our training Division, Moksha Institute o Read More
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