Raland Compliance Partners is a full-service consulting firm supporting life science companies from product concept to commercialization, and beyond. We are focused on providing quality, regulatory, and compliance solutions, along with a full complement of project management and integration services to our clients.
The Partners in our company name refers to the relationships we foster across every aspect of our business. We partner with our clients to understand their challenges and structure projects to provide value-added solutions; we partner with industry leaders and subject matter experts to stay on top of regulatory trends and best practices; and we foster a partner relationship with our employees and contractors to understand their skills and ambitions to provide opportunities for growth and job satisfaction.
We are a service-first organization dedicated to providing the best experience possible. Our employees and associates are seasoned experts, many with FDA service experience, and are adept in the technical and operational aspects of the pharmaceutical, biotech, and medical device industries. Our deep knowledge and strategic insight enable us to skillfully develop and apply solutions.
Headquartered in Chicago, IL with offices in NY, CA, and MD and representative locations in OH, FL, NC, TX, and WI, we have executed projects in more than 30 states and 26 countries. Raland provides quality, regulatory, and compliance consulting services to the pharmaceutical, biotech, and medical device industries.
Our Communications division, Raland Learning, provides custom e-learning and instructor-led training development, training support applications development, and technical writing services.
Our sister organization, Raland Translation, provides document, application, and e-learning translation services as well as in-person, over-the-phone, and video interpretation services.
We help our Life Science clients navigate the increasingly complex landscape of FDA regulations and compliance scrutiny, providing clarity and predictability to enable better outcomes. With an average of 20+ years of industry experience, our management team is adept at developing value-added solutions based on current regulatory requirements and industry best practices tailored specifically to meet your requirements.
Utilizing our extensive industry knowledge, we can react quickly to provide pragmatic solutions to best suit your needs. Whether you need the consulting expertise of an ex-FDA subject matter expert, a full project team, or just some added operational bandwidth, we are prepared to mobilize at a moment’s notice. Whether you are a small start-up or a multinational organization, Raland can provide the solutions for your quality, regulatory, and compliance needs.
With Subject Matter Experts on staff, we are ready to discuss what’s keeping you up at night, regardless how small, and provide an expert opinion or work with you to formulate a solution that fits your compliance needs and risk tolerance.
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At Raland Compliance Partners, our professionals provide a wealth of experience across multiple disciplines within the pharmaceutical, biotech, and medical device industries. Here are just some of the services we provide. Select each one to learn more.