At Red Line we ensure that your business has the best Pharmacovigilance support in the industry

 Latest News

Periodic Safety Update Reports (PSURs) are pharmacovigilance documents intended to provide an evaluation of the ...
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The new EU regulations for medical devices (MDR) and in-vitro diagnostics (IVDR) have been in development since 2012 and ...
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In September, I was invited to attend an international workshop to review the Erice Declaration in Sicily. I was one of ...
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Statistics show that approximately 1.5 million prescriptions are written by general practices in the UK on a daily basis ...
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EU data protection laws prohibits the movement of personal data to non-EU countries, unless that country ensures ...
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So, it’s mid-November and Christmas is creeping up once again. It has been an exceptionally busy year at Red Line ...
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We are proud to announce the company has received ISO9001 accreditation from the British Standards Institute. An ISO ...
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Just received the latest email from the MHRA outlining the ‘MHRA Phase I Accreditation Scheme Requirements’, ...
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If you’re lucky enough to have experienced a pharmacovigilance regulatory inspection, you’ll understand the ...
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I was co-presenting at a medical information training day some months ago and one of the topics under discussion was how ...
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The ABPI Code of Practice has been in effect since 1958 and pharmaceutical companies are expected to abide by the code, ...
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Continued Professional Development (CPD) within the pharmaceutical industry requires considerable investment in terms of ...
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Red Line subscribes to a number of scientific journals, one of my favourites of which is the Drug Safety journal. As a ...
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On 18th June 2012, a concept paper on the introduction of fees charged by the EMA for pharmacovigilance was published by ...
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On the 5th June 2013, Red Line’s Managing Director & QPPV attended the new 3 day course run collaboratively by ...
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We are delighted to welcome on board our in-house physician Nina Patel. Whilst Nina has played a background ...
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In February, Red Line Pharmacovigilance was inspected by the Medicines and Healthcare Regulatory Agency (MHRA), the ...
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The deadline for implementing the new pharmacovigilance legislation within the EU ended on 21 July 2012. The new ...
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Professional enquiry handling to support the safe and effective use of your products. Ease the regulatory burden and keep compliant with current pharmacovigilance legislation. Product safety through surveillance of published articles and case reports. A comprehensive technical review and final signatories for all promotional materials. Confident staff to support the pharmacovigilance process.

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