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  • PPD takes pharmacovigilance to Bulgaria
    In most industries, companies regard the issue of successfully getting products available on a wide scale as the biggest challenge facing them. However, this is not the case in the world of pharmaceuticals, as the projects of drug development firms do not necessarily end when their latest items hit the shelves.
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  • Embracing pharmacovigilance with technology
    It is relatively common knowledge that the pharmaceutical industry must meet a range of guidelines as it works to ensure the safety and effectiveness of the products it develops. However, what is perhaps less known is how such work continues even after new drugs or medicines have reached the market. Pharmacovigilance is used to carry out such projects, but what does it entail?
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  • Is it safe to outsource safety?
    Pharmacovigilance (Drug Safety) is one of those cornerstone activities of any Pharma Company or indeed anyone conducting clinical studies in patients within academia.
    The need to operate a system of pharmacovigilance which is both compliant to the multi-national (and varied) regulations together with the highest principles of patient protection mean that sometimes this places Companies in a dilemma of having products in development or on the market which do not generate many adverse events (side-effects) but when they do require experienced individuals to assess such reports to determine whether the reported events are indeed causally related to the Company product, their seriousness, and whether such events are known already to occur with the product or not (expected or unexpected).
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