For over 30 years, our toxicologists and regulatory affairs specialists have helped guide clients through the complex regulatory hurdles to obtain pharmaceutical and healthcare approvals. We can provide expert advice at all stages of product development for clients in the pharmaceutical, biotechnology, and medical device fields. Supported by our offices in the United States, Canada, and Europe, we work with clients worldwide to develop strategies to effectively meet their urgent and long-term global product development needs. This includes e-publishing for our clients using the LORENZ’s publishing software.
Consulting ServicesPharmaceuticalRegulatory Intelligence