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.
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.