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Excellence in Regulatory Consulting and Medical Writing Services Since 1987

Mission Statement

Hubbell Consulting, LLC provides regulatory consulting, medical/regulatory writing services, and clinical trial management to the pharmaceutical, biotechnology, and medical device industries, and to contract research organizations worldwide.  We strive to apply our experience and expertise in research and development and in regulatory affairs to contribute to these industries and improve human health.  We emphasize quality, collaboration, commitment, communication, respect and responsibility.  We focus on our clients' needs and priorities, adhering to agreed upon timelines and striving to uphold the values of accountability, confidentiality, expertise, excellence, integrity, and reliability.

Company Overview

Since 1987, Hubbell Consulting has built a reputation of excellence in project execution and delivery. The Hubbell Consulting team is comprised of individuals with many years of experience in scientific communications, clinical research, and regulatory affairs. Team members hold degrees in fields such as biology, cell and molecular biology and genetics, psychology, and engineering. All consultants have been trained in Good Clinical Practices and follow ICH guidelines. Consultants are active members of professional organizations such as Regulatory Affairs Professionals Society (RAPS), American Medical Writers Association (AMWA), and Drug Information Association (DIA).

Hubbell Consulting, LLC was founded in 1987 by its president, Howard R. Hubbell, PhD. Dr. Hubbell obtained his Doctoral degree at The University of Texas Graduate School of Biomedical Sciences at Houston and has over 25 years of experience working in the pharmaceutical industry. He also has extensive experience in academia, spending 13 years as faculty in oncology and biochemistry at Hahnemann Medical School. He is involved in numerous professional societies, has served on editorial boards or as an ad hoc reviewer for several journals, and has written over 85 publications and abstracts in the areas of oncology, genetics, AIDS, virology, ophthalmology, biochemistry, and molecular biology.

Our consultants provide services in the areas of research & development, clinical trials, regulatory affairs, and medical writing for pharmaceuticals, biotechnology, and medical devices. Hubbell Consulting has extensive experience in Phases 1-4 of clinical development.