Our Services and Consultation Overview
Pacific Link consultants have decades of experience in the regulatory and clinical development of medical products in the United States, Europe, Canada and Japan. We provide comprehensive work and services that compliment your own staff or we can fully manage your project. From discover and business development, through filings with the FDA, though clinical trial development, and to FDA submission, Pacific Link Consulting can provide you with an entire suite of services.
Learn more about what we do for Clinical Trials here including protocol development, management of the clinical trial process, vendor management, clinical study report development and more.
Learn more about individual Team Members and their years of experience in the new business development, clinical trial development and management and regulatory fields. They also have years of experience working within the regulatory environments of Europe, the United States, Japan and Canada.
Learn more about our Partners. We’ve worked with our experienced partners for many years. With partners based in Europe and the United States, we have boots on the ground expertise in those markets.
Learn more about our Business Development opportunities and how we can work to help your company expand your portfolio of options.
Learn more about what we do for Clinical Trials here