Protocol Link, Inc. is a global project management firm organized to provide comprehensive consulting services for FDA-regulated companies. Since 1996, Protocol Link has offered the best of both quality and efficiency to each one of its clients throughout the United States and 26 countries worldwide. This has been proven by successfully completing over 850 projects, utilizing our core staff of Subject Matter Experts. These projects covered areas of discipline including compliance management, quality systems, regulatory affairs and validation and advised firms ranging from start-ups to several multi-national companies.\\Our team of Subject Matter Experts are dedicated to each and every project. Throughout our 21-year tenure, our SMEs have delivered an array of services, a few of which includes conducting Mock FDA Inspections, Quality Systems action plans and Quality Master Plans, full lifecycle product recall management, cGMP compliance gap analyses, Laboratory Operations and Management, OOS analysis and resolution, change control administration across all production areas, regulatory affairs management, eCTD publishing, submission life cycle management, CDER, CBER and District Liaison, product recall management, championed process validation policies and procedures which encompassed the entire validation lifecycle, test protocols and various IT guidances, and root cause analysis.\\We not only supply the subject matter expertise required to fulfill project goals in this rapidly expanding and evolving industry, we also bring the Project Management expertise to efficiently direct and complete project tasks on time, every time, the first time.\\For more information on Careers visit our webpage, www.protocollink.com, and submit your Application under 'Contact Us'​.

Compliance Management cGMP / QA Documentation Quality Systems Business Solutions Validation / Qualification Technical Services Regulatory Affairs Project Management Medical Device UDI Compliance cGMP Documentation Validation & Qualification Device & Diagnostics Audits Data Integrity Combination Products Technical Writing GxP Services Pharmaceuticals Validation & Qualification Device & Diagnostics Assessments GMP Compliance Venture Capital Deviations and Investigations Major Drugs Pharmaceutical Preparations