ABOUT PHARA

PhaRA is a team of Regulatory Affairs Professionals with a heart and talent for Regulatory Affairs, and a successful track record of interactions with health authorities. PhaRA is committed to meeting each client’s regulatory milestones in drug development to quickly bring medicines to patients and keep approved medicines on the market. By focusing exclusively on regulatory affairs, PhaRA can offer in-depth knowledge, insight, skills, and expertise covering a broad range of regulatory affairs activities throughout product development and life cycle for chemical entities and biologics. With our flexible consultancy services, we offer end2end scope solutions from setting global strategy to writing regulatory, CMC and medical documents, managing global labelling and executing regulatory procedures across the life cycle of a product, device or combination.

PHARA EXTENDS ITS REGULATORY CONSULTANCY SERVICES THROUGH TALENTSHARING

PhaRA wants to provide its clients with driven, flexible people who have a special interest, gene and skill set for regulatory affairs, and who are especially selected to deliver upon that promise. We do not just provide another resource, we provide people who are competent and pleasant to work with. We share our regulatory talent and energy. We are prepared and all buckled up. As a client, you are in the driver’s seat. We simply facilitate your ride on regulatory roads. We deploy people who are used to adapting at a fast pace and who will help you carry your luggage to reach your destination.
Our people will help you flawlessly execute regulatory strategies and activities that you have defined internally. PhaRA talentsharing focuses on embedding its services into the daily practice of the client. It is about sharing resource and talent where this talent is essential.
Our clients will benefit from PhaRA’s long standing experience in regulatory affairs. Our people are selected, educated, trained in-house and coached by senior PhaRA consultants.