Although AI has quite a lot of potential to benefit clinical trials, there are ethical questions it brings up as well. These include bias in AI models, the inability to adequately explain AI assessmen...

One of the major challenges in clinical trials persists in patient recruiting, which typically results in research time delays. Which strategies are often utilized by CRAs and CROs to improve selectio...

Ensuring the safety of healthy volunteers and patients taking part in clinical trials is vital. Another essential component of clinical studies is data integrity. What are the primary ethical and regu...

The choice between Product Development and Product Management depends on individual interests and skills. If someone enjoys technical aspects and problem-solving, product development might be a better...

Securing a sale is only half the struggle in competitive sectors; sustaining long-term connections is essential for fostering repeat business and retaining customers. How can businesses apply customer...

Storytelling has become a popular technique to involve customers on an emotional level and differentiate a brand from its competitors. How can brands use narratives to create strong customer loyalty? ...

To transfer the business to his sons, the father can convert the sole proprietorship into a partnership. This involves creating a new partnership agreement, transferring business assets, and allowing ...

Corporate teams might have separate roles and hierarchies, whereas research labs might have greater disciplinary collaboration and academic freedom. How does it influence the creativity and productivi...

Requiring engineering students to take an additional business course could offer significant benefits, such as a holistic understanding of industry, improved communication and leadership skills, and e...

Embedded software is a common feature of modern medical devices. What QA processes are vital to validate this software to meet regulatory standards?

The maintenance of regulatory compliance relies on audits. What frequent problems arise during internal or external audits of a QMS and how can companies prepare to avoid these pitfalls?

Medical equipment classified as Class III are more risky and require rigorous regulatory approval. How can QA make sure that during the design and development stages the device satisfies these improve...

Clinical trials are necessary for the approval of both medicines and medical devices. However, there are major variations in the design, scale, and scope of device trials. Identifying the differences ...

The FDA regulates e-cigarettes and other electronic nicotine delivery systems (ENDS).They also oversee the contents of e-liquids and the packaging of e-cigarette products, such as requiring health war...

The varying legality of drugs across countries reflects different approaches to drug regulation, risk assessment, and public health priorities. This includes regulatory differences, public health and ...