Pharma Marketing Network

AUGUST 9, 2023

The pharmaceutical industry operates in a highly regulated environment, where marketing and advertising practices are subject to rigorous scrutiny. Navigating these regulatory challenges is essential to ensure compliance, maintain trust, and effectively communicate the benefits and risks of pharmaceutical products.

Marketing 52

Marketing Pharma Food and Drug Administration Media 52

European Pharmaceutical Review

MARCH 12, 2024

Regulatory bodies such as the US Food and Drug Administration (FDA) and European Medicines Agency (EMA) place great importance on data integrity in the pharmaceutical/life science industry. By implementing QMS, companies can ensure that their products and services meet the highest quality standards and are safe for consumers.

Government 86

Government Pharma Ethics Training 86

Pharma Marketing Network

AUGUST 9, 2023

The pharmaceutical industry operates in a highly regulated environment, where marketing and advertising practices are subject to rigorous scrutiny. Navigating these regulatory challenges is essential to ensure compliance, maintain trust, and effectively communicate the benefits and risks of pharmaceutical products.

Marketing 40

Marketing Pharma Food and Drug Administration Media 40

pharmaphorum

OCTOBER 27, 2022

Digital channels are defined as “ platforms for electronic communication through transmission of digital content over the internet or computer networks. The Guidance applies to both product-related and therapeutic-area-related activities. Digital Channels include, but are not limited to, social media ”.

Media 89

Media Pharmaceutical Medicine Electronics 89

European Pharmaceutical Review

APRIL 21, 2023

Hence, every country that looks at decarbonising its health sector – and all EU Member States must – will quickly look at the pharmaceutical industry. In addition, the number of active substances detected in the environment has been increasing with unknown consequences for ecosystems and the accumulation of substances in food chains.

Pharma 79

Pharma Food and Drug Administration Medicine Pharmaceutical 79

European Pharmaceutical Review

JANUARY 16, 2023

This also occupies a large resource, given the US Food and Drug Administration (FDA) requirement for double plate checking using a second ‘independent’ person. Tony Cundell: Perhaps the second greatest challenge is the ongoing transition from products based on small molecules to large molecules to cellular therapies. About the authors.

Pharmaceutical 125

Pharmaceutical Food and Drug Administration Manufacturing FDA 125