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HomeLife SciencesClinical Research ServicesEarly Phase I-IIaRegulatory & Pharmacovigilance
With the combined skills and knowledge of 50 experienced, multilingual specialists with global experience in regulatory submissions and drug safety programs, our team applies its expertise internationally and locally, facilitating the submissions process for the pharmaceutical and biotechnology industries. We draw on the knowledge we have gained from our our close work with regulatory agencies worldwide, including the EMEA and local country health authorities, and we ensure that all of our experts are trained to meet the requirements of the International Conference on Harmonization (ICH), EMEA/CPMP, the FDA and other important regulatory bodies.
As a world leader in Life Science Services, we have over 35 years’ experience as a global contract organization, and we are able to shape our clinical research regulatory compliance services to meet the diverse needs of our clients, from those working on single compounds to those leading a full drug development program.
Whatever your particular requirements, you can choose from a comprehensive range of clinical research regulatory and drug safety compliance services:
Whatever clinical trial submissions or marketing application you are working to complete, SGS can help make them seem less daunting. We always work to the high standard our name has come to be associated with, and every client receives the same levels of integrity and flexibility.