Recall activity in the pharmaceutical and medical device industries went up in Q2 2017 and so did the number of Class I recalls, which the FDA defines as “a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.” In the face of these challenges, companies must look for ways to improve recall effectiveness at the hospital, clinic, and consumer level.
This webinar featured a panel of recall experts, who will share information on recall best practices at every stage of the life cycle, from notification through remedy management and close out with the FDA. It will address the specific recall challenges pharmaceutical and medical device companies face, including working with hospital networks, identifying affected product already in the marketplace, and understanding complex regulations.
Stericycle Expert Solutions is a true business partner — an on-call extension of each customer’s team with a staff standing ready to guide companies through the recall, retrieval, return and audit processes. Our team provides the most comprehensive range of reputation management services across the globe. This comprehensive suite of highly focused services provides global and local expertise before, during and after a recall threat. Stericycle has the right resources in the right locations to manage any recall challenges with speed and accuracy.
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#ICYMI @WSJ @AlexandraBerzon reports courts will decide whether online retailers can be held liable for unsafe prod… https://t.co/qQOIdQa1d9
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