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Pintels Bench to Bed Analytics for Pharmacovigilance, Drug Safety and Risk Management Training Course

Pintels Bench to Bed Analytics for Pharmacovigilance, Drug Safety and Risk Management

Date: Thursday, February 11, 2016
10am-11:30am PST, Online Training
Duration: 90 Minutes
Price: $299 - Includes e-book Handouts!

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Course Description

  • Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. Then the critical question to ask is how do you go about achieving this? This course is designed to provide you hands on learning on how to manage and conduct drug safety monitoring, perform post-market Pharmacovigilance, detect drug safety signals, improve drug safety or create new products & services and assess, manage and mitigate risks. World Health Organization WHO defines Pharmacovigilance as “the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems”. In this course you shall learn the approaches and techniques to enhance drug safety and patient outcomes by leveraging Adverse drug reaction reporting systems, post-market Drug safety intelligence.

    Upon completion of this course, you should walk away with:

    • Introduction to Pintels Bench to Bed Analytics
    • How to identify the risks and the risk factors in the shortest possible time?
    • Establishing collaborative system to share drug, patient and adverse event information and communicate effectively
    • Identifying Adverse Drug Reactions (ADR's)
    • Learn how to leverage comprehensive intelligence for analysis and preventing adverse reactions
    • Assess various factors in improving Drug Safety
    • How to make pharmacoepidemiologic assessment (and safety signal interpretation) of the data regarding OTC, Rx, generic drugs, including biological drug products
    • Learn how to leverage Drug Safety Intelligence to enhance patient safety and learning through failures
    • Conducting Risk Assessment and formulating risk mitigation strategies

Who Should Attend

This course is tailored for Pharmacovigilance teams, Drug Safety experts, Risk Mitigation Strategy teams, R&D Scientists, Pharmacokinetics Scientists, Pharmacodynamics Scientists, Drug Safety Monitoring experts, Medical Affairs, Regulatory Authority teams.

Instructor Bio

Kameshwar Eranki is CEO & Chief Architect of VajraSoft Inc., a Intellectual Property Management Software company based in Silicon Valley, California, helping customers build, manage innovations portfolio and monetize IP's. Kameshwar architected several award winning Cloud, big data and innovations applications, and drives the growth of Products and Customer portfolio. He has over 22 years experience and is responsible for spearheading Intellectual Property Management Software development, process improvement, technology adoption and delivering customer value. He is recognized leader in Big Data Analytics, Cloud Computing and as global Intellectual Property expert.

Kameshwar is experienced in providing transformative innovative solutions to Life Sciences, Green Energy, Automotive, Manufacturing, AgTech, Nutraceuticals, Food Processing, Glass & Chemicals, Aerospace Industries. He is a frequent keynote speaker and panelist at World Patent Congress and Big Data Conferences and has published 11 books in Software programming technologies and Intellectual Property Management. Kameshwar is also IP Columnist and pens articles for leading newspapers and media channels. Kameshwar holds Master of Science in E-Business Systems and Technologies from Golden Gate University, San Francisco, USA. Kameshwar is based in Silicon Valley, California USA.