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The last year and half have been fueled by the hype about the potential of Artificial Intelligence (AI) algorithms in replacing work done traditionally by humans, driven primarily by generative large language models (LLMs) such as ChatGPT. One area of lively debate is the ability of ChatGPT in analyzing health information to generate therapeutic decisions … Read more

Almost all discussions about food-borne illnesses focus on pathogens such as bacteria that may contaminate our food, but what about harmful chemicals? Chemical poisoning may take longer to show symptoms and may cause long-term health issues. However, the FDA has an active and robust program to prevent chemical poisoning from food consumed in the US. … Read more

A question as old as the modern drug industry is about the true benefit provided by new treatments. This is an important argument to justify the high cost of newly approved drugs compared to those available in the prior days and years. A study by researchers in Europe raises some interesting questions about the added … Read more

A survey by the General Accountability Office (GAO) reported many interesting facts about the state of clinical trial audits by the FDA inspectors. The purpose of the GAO survey was to identify deficiencies in the FDA audits for compliance with Good Clinical Practices (GCP), but in the process, it reports several surprising facts about the … Read more

A medical device company had to suspend its ongoing pivotal clinical trial and may lose the data collected in the trial so far because of major violations of Good Clinical Practices (GCP) found during an FDA audit. The Warning Letter issued to the company looks like a lesson in the basics of GCP compliance for … Read more

For the last few months, a new Law, called the Biosecure Act, has been gaining bipartisan support in the US Congress, which aims to ban business with Chinese biotech companies, the biggest of them WuXi companies. The law could have some serious consequences for the US customers of these companies. WuXi, which owns a few … Read more

FDA’s previous guidance on cybersecurity aspects of internet connected medical devices provides a detailed description of all the issues that manufacturers must address prior to filing their market approval applications with the FDA. This week the FDA released an update to a few sections of that guidance which would likely require updates to the market … Read more

It is not uncommon for sponsors to use research labs in academic settings for specialized clinical tests not available commercially. However, the convenience of using such labs comes with its own challenges particularly when the sponsor does not follow common sense measures to ensure the quality and reliability of the tests conducted at these labs, … Read more

Experimental data from research in non-human primates, which is almost always rhesus monkeys, is considered critical for establishing the safety and efficacy profile of many new drugs in market approval applications to the FDA. So, the ethical and legal acquisition of animals for this research is an important consideration. This week, an expose in Bloomberg … Read more

There are a few important considerations for the Informed Consent Document (ICD), also called the Informed Consent Form (ICF), used by sponsors to consent clinical trial participants which could improve the quality of the consent process and possibly increase trial participation. The design of the ICD varies extensively due to the experience of the sponsors … Read more