PrimeVigilance - pharmacovigilance

May 3, 2012


PrimeVigilance's Perspective on the New Pharmacovigilance Legislation. The new pharmacovigilance legislation in July of this year will be the biggest change to medicines legislation since the creation of the current European system in 1995.

 
Feb 22, 2012


PrimeVigilance Commercial Director Jon West is attending DIA 2012 48th Annual meeting.
Visit us at our booth number 1931 and meet Jon

 
Feb 22, 2012


PrimeVigilance Commercial Director Jon West is attending DIA 2012 24th Euro Meeting
Visit us at our booth number 221/223 and meet Jon.

 
Oct 27, 2011


Guildford, UK 25th October 2011 PrimeVigilance Limited today announced that it has established a Cambridge, UK office and has also recruited additional senior managers to its management team. The latest recruits include Natalie Smith (ex-Shire) as Director of Operations and Beverly Gow (ex-Novartis) as Pharmacovigilance Manager.

 
Sep 26, 2011


Guildford, UK 15 September 2011, PrimeVigilance is pleased to report that Giovanni Furlan,  Director of Pharmacovigilance Consulting and QPPV, has participated in the writing of three technical papers.

 
Sep 15, 2011


PrimeVigilance is pleased to report that Dr. Elliot Brown, a PrimeVigilance founding director has participated in the writing of three technical papers.

 
Jun 15, 2011


June 19 -23, 2011
Chicago, IL - McCormick Place

PrimeVigilance Commercial Director Jon West is attending DIA 2011



Visit us at booth 238 and meet Jon.

 
Dec 14, 2010


Guildford, UK 14 December 2010, PrimeVigilance is pleased to report that Giovanni Furlan, a PrimeVigilance senior manager and QPPV, has participated in the writing of two technical papers. PrimeVigilance is committed to participating in discussions at the forefront of developments in the field of pharmacovigilance and welcomes questions and comments from interested parties.

 
Jun 30, 2010


PrimeVigilance announces opening of offices in Krakow, Milan and Zagreb in line with its strategy of setting up a Europe-wide operating structure from its Guildford head office. In response to market demand PrimeVigilance has expanded its team of pharmacovigilance specialists and now has almost twenty active staff, as well as a global team of consultants, supporting pharmacovigilance and clinical safety assignments.

 
Feb 2, 2009


Founded by two globally respected experts, the newly formed PrimeVigilance Ltd. provides a unique offering in the field of pharmacovigilance (PV).

 

PrimeVigilance takes pharmacovigilance services (PV) to the next level, providing peace of mind to its clients:

Whether your company needs a full, cost-effective pharmacovigilance system, or just a Periodic Safety Update Report (PSUR), PrimeVigilance has the solution.




Pharmacovigilance operations and Pharmacovigilance consulting: Compliance and Professionalism

 

PrimeVigilance's pharmacovigilance services

PrimeVigilance's expertise encompasses both pre and post marketing pharmacovigilance.

Effective processing of clinical trial safety data is imperative to the successful conduct of a clinical trial. With years of experience in clinical trial management PrimeVigilance offers effective management of clinical trial SAEs from case assessment through to expedited reporting of SUSARs (Suspected Unexpected Serious Adverse Reactions) to the regulatory authorities as well as Annual Safety Reports (ASRs) which have to be submitted to regulatory authorities and Ethics Committees throughout the course of the clinical trial programme. PrimeVigilance can take care of all of your Clinical Trial Safety requirements, including forming a data safety monitoring board.

Once your company holds a marketing authorisation, regulatory requirements change. PrimeVigilance is able to take care of all of your requirements for case processing, expedited reporting, periodic safety update reports (PSURs), literature screening and safety signal detection and review - in fact we can provide and run your entire pharmacovigilance operation.

PrimeVigilance can provide the EU Qualified Person for Pharmacovigilance, and a validated ARISgTM safety database, electronic reporting to Eudravigilance along with preparation of your DDPS (Detailed Description of Pharmacovigilance System), your Standard Operating Procedures and safety data exchange agreements. We are uniquely placed to be able to provide top specialist assistance such as the production of risk management plans (RMPs), responding to regulatory enquiries, helping with assessment of benefit and risk and assisting in responding to safety concerns. We also carry out training, including inspection preparedness training and have world class experience in performing audits. We can then can help you implement any corrective actions that may be necessary. PrimeVigilance offers all the component parts needed to help ensure drug safety, for your compliant and effective pharmacovigilance system.

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For more information contact PrimeVigilance today


 

PrimeVigilance

in conjunction with Elliot Brown Consulting and Ergomed