# Regulink: Regulatory Affairs & Pharmacovigilance Specialist

Regulink is a Redhill-based regulatory affairs consultancy providing urgent, responsive support to pharmaceutical and life sciences companies facing tight deadlines and resource constraints. The business specialises in delivering expert regulatory and pharmacovigilance solutions when internal teams lack capacity or external providers cannot respond quickly enough.

The company serves pharmaceutical organisations, biotech firms, and medical device companies navigating complex regulatory requirements across multiple disciplines. Their core strength lies in mobilising highly qualified specialist teams on demand, bridging gaps between project urgency and talent availability.

Regulink distinguishes itself through three fundamental pillars: responsiveness (delivering support without unnecessary delay), innovation (applying bespoke solutions and automation to regulatory challenges), and quality (engaging only proven experts known for excellence in their specialisms). Rather than offering generic off-the-shelf solutions, they tailor their approach to each client's specific needs.

The business covers the full regulatory spectrum—from pre-clinical and clinical services accelerating pipeline development through to post-market pharmacovigilance and medical information support. Their in-house Qualified Person for Pharmacovigilance (QPPV) ensures expert oversight of safety obligations. They also provide product training and support CMC (Chemistry, Manufacturing, Controls) compliance.

Regulink's value proposition centres on solving the talent acquisition problem: accessing specialist regulatory expertise rapidly without recruitment timescales, making them ideal for peak workload periods, emergency projects, or filling expertise gaps.