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The Food and Drug Administration (FDA) plays a critical role in regulating the pharmaceutical industry and ensuring that medications and medical devices marketed to the public are safe, effective, and appropriately labeled. However, in recent years, there has been a noticeable decline in the number of these letters being issued.
The Guidance applies to all member companies of EFPIA and IFPMA, but also acts as useful guidance for all pharmaceuticalcompanies as to how the authorities will interpret the legislative provisions to social media channels. However, the involvement of the company should always be stated.
Navigating these regulatory challenges is essential to ensure compliance, maintain trust, and effectively communicate the benefits and risks of pharmaceutical products. In this blog post, we will explore best practices for pharmaceuticalcompanies to navigate the complex landscape of regulatory challenges in marketing.
Navigating these regulatory challenges is essential to ensure compliance, maintain trust, and effectively communicate the benefits and risks of pharmaceutical products. In this blog post, we will explore best practices for pharmaceuticalcompanies to navigate the complex landscape of regulatory challenges in marketing.
Specifically, pharmaceutical secondary packaging is a vital step in the product supply chain as it encloses life-saving drugs and therapies, preserving the identity, quality, integrity and stability of the packaged drug product. [1] 3] Some of the advantages offered by pharmaceutical secondary packaging have been depicted below.
In order to ensure that this critical aspect is maintained, the pharmaceuticalcompany should carry out a detailed evaluation of the quality control and quality assurance departments of the CMO partner. Chances of de-prioritization: Usually, CMOs are involved in multiple projects and agreements with different pharmaceuticalcompanies.
Further, pharmaceuticalcompanies are also becoming cautious towards optimizing various operations for packaging, which can indirectly help in reduction of raw material and energy consumption. To avoid such instances, various guidelines have been issued by regulatory authorities.
Promoting content worldwide When a pharmaceuticalcompany publishes content, it often considers the norms and laws of the country in which it operates. But what if this company decides to expand worldwide? The truth is that MLR reviews are needed in 90% of cases, whether it is a website blog post or an important research paper.
The government acknowledges the strategic importance of such investments in bolstering the country’s standing in the global pharmaceutical landscape. To address this, the company has taken measures such as restricting access to lower starting doses of Ozempic in the European Union and the United States.
This may include blog posts, whitepapers, videos, podcasts, or infographics. The most suitable formats for pharma are eDetailers, infographics, case studies , blog posts, articles, and so on. For example, blog articles and social media posts may be most effective during awareness.
Takeda is the first pharmaceuticalcompany worldwide to have implemented this water preservation project, in collaboration with a Belgian start-up Ekopak, on a large scale. Their overall goal is to reduce freshwater withdrawal by 90% by 2027 (the equivalent of 600 million liters of freshwater).
We may do some things like you were talking about where we have advertorials, and it’s clearly labeled as an advertorial. RJ Lewis (EHS): So today everybody’s a publisher, part of the beauty of the web and even if you don’t have the technical skills for firing up a website or a blog, which is pretty easy.
The letters come on the heels of FDA finalizing its Guidance on Presenting Quantitative Efficacy and Risk Information in Direct-to-Consumer Promotional Labeling and Advertisements. Both letters addressed quantitative efficacy presentations—attacking the numbers as well as the underlying methodology for obtaining those numbers.
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