All Blog Posts (1,642)

https://globalcompliancepaneltraining.files.wordpress.com/2018/01/the-fda-export-reform-and-enhancement-act-of-1996-a-brief-understanding-3.jpg?w=150 150w,…

https://globalcompliancepaneltraining.files.wordpress.com/2018/01/effective-complaint-handling-guidelines-serve-as-a-basis-for-improvements-in-medical-devices1.jpg?w=150 150w" sizes="(max-width: 266px) 100vw, 266px" />Far from being frowned upon, complaints should serve as…

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For many years before the advent of automation and computerization ,…

There is enormous potential for digital marketing for pharmaceutical companies. Proper exploitation of the social media can take pharmaceutical companies to their market in a more pinpointed and accurate manner than traditional marketing.

Gone are the initial days of reluctance on the part of pharmaceutical companies to…

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The beginnings of all that the USFDA regulates can be traced right to the early decades of the founding of the nation. In a sense, the FDA, even if came to be called by that formal name much later; embodies the discipline and value set that the new created nation sought to represent. Regulation of all aspects of American life was deeply ingrained…

Good Documentation Practices are the soul of many regulated industries. The FDA, like all other regulatory agencies, makes GDP a central element of its regulations, and bases it on the principle of evidence. For the FDA and other regulatory agencies across the world, what is not documented is nonexistent.

Good Documentation…

Sponsors of clinical studies adapt many methods that are aimed at reducing the complexity of clinical trials. They also look for methods by which they can increase the efficacy of the results, while keeping the costs low. Risk-based monitoring is one of these methods.

How is risk-based monitoring understood?One can understand risk-based monitoring in several ways. This varied understanding is because there is no one definition or…

As the primary regulator of the biological, healthcare, life sciences and other related industries; the FDA has power and authority over how its work is carried out. FDA Warning Letters are among the primary mediums through which it enforces its authority.

The FDA issues a Warning Letter to a company when it determines, following…

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