Regulatory Focus™ > News Articles > In Focus: Postmarketing Compliance Activities

In Focus: Postmarketing Compliance Activities

Posted 01 September 2009 | By

It is well known that postmarket activities are the most resource-intensive phase of a pharmaceutical or medical device product's lifecycle. This phase includes not only marketing and pharmacovigilance/vigilance activities, but also the upkeep and maintenance of the license. License maintenance activities include applying for variations and following up on specific obligations and measures. Companies need to exercise strict control over their change management systems to avoid compliance issues.

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