PV Data Base Management

There is an advantage in centralising all safety data, clinical data, analysis and reporting with one provider. Pharmacovigilance Software tool provides comprehensive analysis of adverse events arising from the use of Pharmaceutical products (Medicinal Product, Medical Device, Vaccines, Non-Drug Therapy and Veterinary Medicinal Product). The drug safety database allows the risk- benefit analysis of medicinal products taking into account new and emerging information, in the context of cumulative information. Pharmacovigilance since beginning has been a compliance driven activity, wherein your regulatory compliance determines company’s risk assessment scores. A drug safety database offers scheduling of alerts for expedited cases, follow-up cases and PSUR/PADER reports submission to meet regulatory timeline compliance.

  • WebVDME Pharmacovigilance Signal Detection and Signal Management Software
  • Argus
  • Aris G
  • Clintrace
  • PVNET
  • Post authorisation safety and efficacy studies
  • RepClinical
  • Oracle AERS
  • Periodic safety update reports

Related Conference of  PV Data Base Management

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2nd International Conference on Pharmacognosy

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8th International on Pharmacy and Pharmaceutical Conference

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35th Annual European Pharma Congress

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18th European Biosimilars Congress

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18th World Drug Delivery Summit

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19th World Drug Delivery Summit

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3rd Global Online Summit on Nanoscience and Nanotechnology

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38th World Congress on Pharmacology

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10th International Conference on Future Pharma and Innovations

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4th World Conference on Pharma Industry and Medical Devices

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4th World Congress on Precision and Personalized Medicine

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January 25-27 2016

Pharmacovigilance and Risk Management Strategies 2016

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Medical Aspects of Adverse Drug Reactions

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6th Annual Pharmacovigilaance and Risk Management Strategies

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8th annual Pre-Filled Syringes Conference and Exhibition 2016

London UK
January 28-31 2016

13th Annual Natural Supplements An Evidence-Based Update 2016

San Diego USA
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DSURS and PBRERS 2016

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February 23-25 2016

Summit for Clinical Ops Executives

Miami FL US
February 1-2 2016

Raw Material Requirements Health Canada USP EP in a cGMP Environment - Issues and Solutions 2016

Orlando FL USA
February 4-5 2016

Why is FDA at my facility and what do I do during an inspection 2016

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February 9-11 2016

Ageing 2016

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February 10-12 2016

4th Annual Global Medical Meetings Summit 2016

Philadelphia USA
February 23-24 2016

2nd Annuals Downstream Processing World Congress 2016

Munich Germany
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6th Medical Affairs Leaders Forum Europe Spring 2016

Berlin Germany
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BioFach 2016

Nuernberg Germany
February 11-12 2016

Targeted Drug Delivery 2016

Basel Switzerland
February 11-12 2016

13th Annual High Content Analysis 2016

San Diego USA
February 15-16 2016

15th annual Advances and Progress in Drug Design 2016

London UK
February 19-21 2016

LDN 2016 AIIC Conference

Orlando USA
February 21-24 2016

Long Noncoding RNAs 2016

Santa Fe USA
February 21-25 2016

Assoc for Mass Spectrometry Applications to the Clinical Lab MSACL 2016

Palm Springs USA
March 6-11 2016

Molecular Med Tri-Con 2016

San Francisco CA USA
April 20-21 2016

8th annual World Drug Safety Congress

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April 20 - 22 2016

ABA Risk Management Conference

Grand Hyatt San Antonio TX
April 5-7 2016

Successful Medical Writing 2016

Barcelona Spain
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18th International Pharmacovigilance Training Course

Uppsala Sweden
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18th International Conference on Pharmacovigilance and Drug Safety

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Outsourcing in Clinical Trials East Coast 2016

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The 2nd Conference on Pharmacovigilance and Drug Safety

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29th ECNP Congress 2016

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Keeping Up-To-Date as a GMP Qualified Person 2016

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