Literature Management for Pharmacovigilance and Medical Affairs Professionals

Who uses QUOSA?

Pharmacovigilance and drug safety professionals

You need to screen scientific literature and triage for adverse events related to your products so that they can be promptly reported for regulatory compliance. With QUOSA, you can efficiently monitor safety-related literature and establish a product literature database so you can organize and store relevant articles for compliance reports, including PSURs, ICSRs and more.

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Pharmacovigilance and drug safety professionals

Medical affairs and medical science liaisons

Medical affairs and medical science liaisons

You need direct access to the latest literature so you can rapidly respond to client inquiries from anywhere. Access our central repository from your PC, Mac or iPad and find information quickly and easily – all in one place.

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Medical device companies

You need to monitor scientific literature for mentions related to your products for clinical evaluation reports, pre-market approval and adverse events reporting. With QUOSA you can track and download relevant mentions within full-text articles, review them from your central library and easily create compliance reports.

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Medical device companies

Information managers and corporate librarians

Information managers and corporate librarians

You need an information management solution that can promote current awareness, boost workflow efficiency and reduce waste. QUOSA is easy to customize to fit your needs, making literature easy to access and share, all within our copyright-compliant environment.

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QUOSA iPad app

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