Safety and efficacy are core considerations throughout discovery, development and beyond.
We work with regulators to develop prescribing information for our medicines that provides healthcare professionals and others with the benefit/risk information they need to make prescribing decisions.
After launch, we continue to monitor all our medicines for side effects, including those that may not have been identified during the research and development process. We notify the appropriate authorities about side effects of which we become aware and co-operate with them in taking any necessary action.
Every stage of the research, development, manufacture, storage and distribution of our products (and any active pharmaceutical ingredients) must be conducted in accordance with all applicable internal and external standards.
The Company also works to combat the growing problem of counterfeit drugs, which can adversely affect the health and wellbeing of millions of people worldwide.
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Comply with all applicable procedures designed to promote product safety, efficacy and quality, such as Good Laboratory, Good Clinical and Good Manufacturing Practice.
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Report any incidents of non-compliance.
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Report any possible adverse effects relating to our medicines through the established procedures.
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Report any counterfeit or suspected counterfeit drugs through the established procedures.
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