Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Regulatory, toxicology and scientific consulting expertise for the pharmaceutical and medical device industries.
Intertek’s pharmaceutical and heathcare consultants and experts 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 provide expert advice and services related to nonclinical safety testing, manufacturing, clinical trial design, submission preparation, regulatory agency interactions, and more. Supported by our offices in the United States, Canada, Europe and Asia, we work with clients worldwide to develop strategies to effectively meet their urgent and long-term global product development needs.
Pharmaceutical Consulting Services:
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