Our team consists of highly qualified medically professionals and skilled experts who are committed to help life sciences companies meeting the regulatory expectations timelines by maintaining and safety and risk management of their products.

What we do the best ?

At PharmaMentors we have dedicated and qualified team of professionals, proficient in carrying out Pharmacovigilance services such as:


We segment the process of adverse reporting for pre- and post-marketing cases into five steps: Case Intake, Case Processing, Quality review, Medical Assessment and Submission.

Aggregate Reports

We have a unique modular approach to aggregate reporting activities that emphasizes an organized effort in the writing of PBRERs, PADARs, DSURs and other aggregate reports.

Signal Detection & Management

Our highly medically professional teams support pharmaceutical companies with adopting signal management processes, consisting of detection, validation, confirmation, analysis and prioritization, assessment, and recommendation for action in accordance with legal requirements.

Literature Review

We have a fully customizable literature monitoring and tracking tool that ensures organizations have timely access to reliable and consolidated information on relevant safety-related literature.

Risk Management Plans

The Risk Management program begins with the assessment and identification of risks and potential risks associated with a product.

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