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 and healthcare field. Supported by our offices in Canada, the United States, and global partners, we work with clients worldwide to develop strategies to effectively meet their urgent and long-term global product development needs. We also offer comprehensive end-to-end Regulatory Electronic Submission Publishing services.