Medical Writing & Pharmacovigilance Services

In today’s dynamic regulatory landscape, skilled regulatory medical writing and pharmacovigilance services can add a lot of value to an organization’s overall goal.

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Medical Writing & Pharmacovigilance Services

Medical writing and pharmacovigilance are highly specialized fields that involves collating diverse information from clinical trials, safety reports and other key documentation, with the goal of transforming them into submission ready scientific documents and life cycle management of the products in a comprehensive and convincing manner. In today’s dynamic regulatory landscape, skilled regulatory medical writing and pharmacovigilance services can add a lot of value to an organization’s overall goal.

AARIYA’s medical writing and pharmacovigilance specialists have comprehensive understanding of clinical trial lifecycles and drug safety with expertise in multiple therapeutic areas and product types. Our team has a wide breadth of knowledge and experience drawn from the pharmaceutical and medical devices industry, clinical research organizations, and academia.

AARIYA can assist your organization with following strategic services which includes regulatory medical writing, pharmacovigilance as well as scientific communications:

Regulatory Medical Writing

Drug Safety and Pharmacovigilance

Clinical Trial Disclosure

Scientific Information and Communications

Vision

To become a noble regulatory consultancy, delivering high quality regulatory support to clients for introduction of wide range of generic and branded products in the market.

Mission

We thrive to provide quality focused and flexible services to the utmost satisfaction of our clients building long-term relationship.

Values

Success and strength of any company rests on its strong beliefs and values. We believe in Customer service excellence, Uncompromising quality, Ethics and integrity

Our Client’s Testimonials

    Manager-Regulatory AffairsHead of Regulatory Affairs
  • Aariya’s seamless support in arranging quality labeling, technical inputs, quality review, and most importantly their short turn-around time helped us in timely response to the FDA thereby assisting in securing faster product approval.
    Manager-Regulatory Affairs
    A Malaysian Based Generic Pharmaceutical Company
  • They are great with their prices and excellent with their turn-around times. The most important quality that I like about Sachin and his team is that they would go that extra mile to get the job done and have so far never let us down.
    Head of Regulatory Affairs
    A US Based Generic Pharmaceutical start-up