Regulatory, toxicology and scientific consulting expertise for the pharmaceutical and medical device industries.
Intertek’s pharmaceutical and healthcare consultants provide assistance at all stages of product development to clients in the pharmaceutical, biotechnology and medical device fields.
With diverse and in-depth experience, our team of scientists and regulatory affairs specialists provides expert advice and services related to nonclinical safety testing, manufacturing, submission preparation, regulatory agency interactions, risk/safety assessments, medical writing, and more. We work to develop strategies and deliver solutions that effectively meet our clients' urgent and long-term global product development needs.
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