There is a whole sea of CROs and medical/pharmaceutical groups that are looking for all types of participants to participate in one of their clinical trial. Each study having its own inclusion/exclusi...

Given my background in research, medical devices, and clinical trials, I feel that I would be able to take on any role comfortably after the typical training and learning curve procedures. However, in...

From my internship at a CRO, I was able to observe the workings of phase 1 and 2 clinical trials that were happening. For the study in its second phase, I was able to witness a developed drug undergo ...

I think this is an interesting question to pose for those with or without entrepreneurship ambitions. I think most biopharama or medical device companies share a similar mission objective in the sense...

Like many of the posters above, I would also like to reiterate the importance of the sales and marketing team behind any product's development and marketability. It is important for any product to be:...

In a business perspective, I believe that a company should consider run their advertisements based on the general demographic of a specific channel. For example, advertisements for toys or games could...

I like alot of the points mentioned above arguing for both sides. On one hand, I strongly agree that it is not ethical to establish large margins for medical products that consumers would find to be a...

From the state/government perspective, I worked for a non-profit organization that focused on providing kids with physical activity and lunches during the summer. The way they handled their finances w...

I completely understand the point of view you are conveying. I too always thought it was a bit strange that whenever there is any type of legal issue or controversy in regards to a corporation's actio...

I absolutely believe that when a client is requesting a contract company to build out a medical device, it is absolutely necessary and recommended that the client come in as needed to observe, measure...

I completely agree with the synopsis and iteration of significance of quality assurance and control, but I would also like to add that regulatory affairs is equally important in maintaining that the c...

I personally have familiarity working on quality, specifically in the medical device industry. In quality assurance, the management and verification of Corrective Action Preventive Action (CAPA) is es...

MDSAP has its benefits and disadvantages that the other users described above. I won't be going into that since most of it will be a repeat of what they said. What I would like to address is a typical...

I absolutely believe that the slow moving process of the FDA approval process of a medical device is a sign that the system works. It is the FDA's duty to ensure that every product out on the has been...

To my knowledge, general regulations and restrictions on what is the acceptable threshold or guidelines for a medical product should already be listed on the federal website. Of course, not all medica...