About

PhaRA is a boutique consultancy firm with 20+ years successful track record in submission and approval of regulatory applications and interactions with regulators in the EU. We provide a personal and regulatory-wise service for the development and life cycle management of innovative products to client companies ranging from start-up biotech to Top 10 pharma companies. PhaRA is committed to meet client regulatory milestones in drug development, bringing medicinal products, devices or combination to patients, and keeping approved products on the market. By focusing exclusively on regulatory affairs, PhaRA can offer in-depth knowledge, insight, skills, and expertise, covering end2end scope from setting global strategy to writing regulatory, CMC and medical documents, managing global labeling and executing regulatory procedures in EU and with WHO across the product life cycle.