Search Results for "Pharmacovigilance Conference"

08:51 EST 26th November 2014 | BioPortfolio

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BioPortfolio - life science, medical devices and pharmaceutical conference

BioPortfolio is an internet agent for Visiongain's life science, medical devices and pharmaceutical conference.

Management Forum - highest quality conference, seminar and knowledge-based experiences

Since 1983, Management Forum have built a reputation on providing the highest quality conference, seminar and knowledge-based experiences for leading professionals in some of the world's most...

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Extending the Scope of Pharmacovigilance Comes at a Price

As the pharmacovigilance infrastructure becomes more entrenched in Europe, drug manufacturers are beginning to feel the burden of its high cost.

Download: A successful path to fulfilling Pharmacovigilance obligations

  As the number of innovator pharmaceutical and generic manufacturer partnerships grow, the lines of responsibility for meeting pharmacovigilance requirements can get blurred. This whitepaper ...

EMA guideline on pharmacovigilance inspections comes into effect

As the EMA has announced that the main objectives of its pharmacovigilance legislation are largely being achieved , the agency is still implementing a number of the individual modules that make up the...

Download: Proactive Pharmacovigilance – A New Model for the 21st Century

Whitepaper courtesy of Sciformix 21st century technologies will create significant opportunities and challenges for all health care stakeholders. Pharmacovigilance too is in transition, with new sourc...

PrimeVigilance Limited upgrades its validated databases for pharmacovigilance and medical information - ARISg™ and agInquirer™.

Published date:  28/10/2014 Summary:  PrimeVigilance Limited upgrades its validate...

Highlights of EMA Pharmacovigilance unit meeting

At its meeting last week, the European Medicines Agency’s Pharmacovigilance Risk Assessment Committee (PRAC) made recommendations on products that contain Factor VIII and discussed a fatality in a p...

Highlights from EMA Pharmacovigilance October meeting

At its October meeting, the European Medicines Agency’ Pharmacovigilance Risk Assessment Committee (PRAC) concluded three safety reviews.

Promoting Drug Safety through Latest Advancements in Pharmacovigilance

OMICS Group is delighted to announce the 3rd International Conference and Exhibition on Pharmacovigilance & Clinical Trials on October 27-29, 2014 at Hyderabad India, with the theme "Safer Dr...

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Need for involving consumers in Nepal's pharmacovigilance system.

In Nepal, reporting of adverse drug reactions (ADRs) occurs on a voluntary basis by doctors, pharmacists, nurses, health assistants, and other healthcare professionals. The country's pharmacovigilance...

Effect of educational intervention on adverse drug reporting by physicians: a cross-sectional study.

In India, the pharmacovigilance program is still in its infancy. National Pharmacovigilance Program of India was started for facilitating the pharmacovigilance activities. The ADR reporting rate is st...

Pharmacogenovigilance: a pharmacogenomics pharmacovigilance program.

In this report, we review the importance of pharmacovigilance in detecting postmarketing adverse drug events and the potential for developing pharmacogenovigilance programs by integrating pharmacogeno...

A Description of Signals During the First 18 Months of the EMA Pharmacovigilance Risk Assessment Committee.

New pharmacovigilance legislation in the European Union has underlined the importance of signal management, giving the European Medicines Agency's newly established Pharmacovigilance Risk Assessment C...

Risk management plans as tool for proactive pharmacovigilance: a cohort study of newly approved drugs in Europe.

Risk Management Plans (RMPs) have become a cornerstone in pharmacovigilance of new drugs in Europe. The RMP was introduced in 2005 to support a proactive approach in gaining knowledge on safety concer...

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