Regulatory News

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Real World Data (RWD) vs Real World Evidence (RWE)

by Srikanth Nadig | Aug 5, 2021 | Blogs

Real World Data (RWD) Real World Data is a by product of the everyday usage of products by patients. These data can be collected via various channels such as patient registries, electronic health records, insurance databases, social media, patient research networks...

Pharmacovigilance – Should You Outsource?

by ALG Associate | Mar 11, 2021 | White Paper

The law governing pharmacovigilance lay down rigid details on what pharmaceutical firms must do in the event of analysing a serious adverse event and indeed what constitutes a serios adverse event. With these major demands on pharmaceutical firms, its essential for...

Effect of COVID-19 on Pharmacovigilance & How global Life Science companies can be better prepared during the pandemic

by Anusha Thorati | Jun 9, 2020 | White Paper

Pharmacovigilance Pharmacovigilance (PV) is defined as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. Background: WHO established its Program for International Drug...

WHAT IS THE RIGHT OUTSOURCING STRATEGY FOR YOUR COMPANY? Not One Model Fits All

by Jill Robinson | May 26, 2020 | White Paper

Introduction Pharmacovigilance (PV) is fundamental to the Pharmaceutical and Biotech industries. More now than ever, safety regulations are numerous and complex around the world. Regulatory authorities are requiring more safety documentation and review for...

Harnessing the power of Artificial Intelligence for KOL Engagement

by Thirupathi Ponaganti | Mar 11, 2020 | Blogs

Harnessing the power of Artificial Intelligence for KOL Engagement Recent surveys have shown that pharmaceutical companies and the industry in general is challenged with over 50% failures of new drug launches. This has led to Medical Affairs requiring reinventing to...

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