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03:03 EDT 26th June 2017 | BioPortfolio

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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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Extrapolation and pharmacovigilance for biosimilars

The issue of extrapolation and pharmacovigilance for biosimilars was discussed in the presentation [1] of Dr Dr Martina Weise, Head of the Licensing Division at the Federal Institute for Drugs and Med...

Oviya MedSafe conducts seminar and workshop on pharmacovigilance as part of its 5th anniversary

As part of its 5th anniversary, the Coimbatore─based pharmacovigilance consulting and drug safety services company, Oviya MedSafe (OMS), is conducting a two─day national level conference and works...

Dutch To Score Companies On Their Pharmacovigilance Systems

The Dutch health inspectorate is asking pharmaceutical companies with products on the market to answer questions about their pharmacovigilance systems...   

India needs to build indigenous drug safety database: Pharmacovigilance expert

There is a need for collaboration between IT industry, DCGI and CDSCO to build robust electronic database for Pharmacovigilance Programme of India (PvPI) according to Moin Don, a leading pharmacovigil...

TransCelerate calls out pharmacovigilance operational challenges

TransCelerate BioPharma has added Pharmacovigilance to its portfolio, establishing two new global initiatives: 1.) Interpretation of Pharmacovigilance Regulations and 2.) Value of Safety Informati...

#jobs #lifescience Pharmacovigilance Sr. Scientist

// MA-Cambridge, Our client, a leading fortune company is looking for a Pharmacovigilance Sr. Scientist in their organization. This is a 4 months contract position and is located in Cambridge, MA Top ...

EMA’s pharmacovigilance unit PRAC concludes one safety referral and starts two others

At its meeting this week, the Pharmacovigilance Risk Assessment Committee (PRAC) of the European Medicines…

Dutch IGZ request to marketing authorization holders: questionnaire for pharmacovigilance

The Dutch Health Care Inspectorate (IGZ) has developed a risk model for pharmacovigilance to obtain more…

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What Can Big Data Offer the Pharmacovigilance of Orphan Drugs?

The pharmacovigilance of drugs for orphan diseases presents problems related to the small patient population. Obtaining high-quality information on individual reports of suspected adverse reactions is...

The Potential Return on Public Investment in Detecting Adverse Drug Effects.

Many countries lack fully functional pharmacovigilance programs, and public budgets allocated to pharmacovigilance in industrialized countries remain low due to resource constraints and competing prio...

Effectiveness of pharmacovigilance: multifaceted educational intervention related to the knowledge, skills and attitudes of multidisciplinary hospital staff.

Most educational interventions in pharmacovigilance are designed to encourage physicians to report adverse drug reactions. However, multidisciplinary teams may play an important role in reporting drug...

Outcomes From the First 6 Years of Operation of the Central Portugal Pharmacovigilance Unit.

The aim of this study was to analyze and characterize the outcomes of the Central Portugal Regional Pharmacovigilance Unit over a 6-year period.

A review of the National pharmacovigilance system in Malta - implementing and operating a pharmacovigilance management system.

Regulatory authorities have a legal mandate to implement and maintain a Pharmacovigilance System designed to monitor the safety of authorised medicinal products and detect any change to their risk-ben...

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