Forum Replies Created
RE: FDA classification for bme devices It is always important to know the distinction between the three classes, as stated multiple times in the lecture and the mini simulation because it can lead to many avoidable expenses and loss of tim... |
In forum Introduction to Project Management |
1 year ago |
RE: Project Management Information Systems It is extremely vital to ensure that project progress is met for the project timeline to not be delayed or impacted at all. While ensuring that project responsibilities have been distributed according... |
In forum Introduction to Project Management |
1 year ago |
RE: Reclassifying Medical Devices This is a very interesting topic because how possible it is in the "real world" for industries to experience something like this during projects. Based off the lectures and mini simulation this week, ... |
In forum Introduction to Project Management |
1 year ago |
RE: Funding in Medical Devices Industry While many have stated that the company should fund the project and go for the patent, the initial post only says that the project idea has a potential to be patented in the future. In the medical dev... |
In forum Introduction to Project Management |
1 year ago |
RE: How to increase emotional intelligence The part of the lecture that focused on emotional intelligence and social skills really stood out to me and made me want to start reading the novel that was mentioned in the lecture. Similar to what o... |
In forum Introduction to Project Management |
1 year ago |
RE: Sizes of Project Teams I found it very interesting reading the different opinions and experiences of others that have been part of project management teams. From my personal experience at a medical device company and being ... |
In forum Introduction to Project Management |
1 year ago |
When is giving gifts like the "old days" too much? This week's lecture discussed the "older days" strategy where a physician would be given lavish gifts such as vacation trips or lavish dinners. Essentially, doctors were being using products they were... |
In forum Consultants and Legal Basics |
3 years ago |
RE: What are the limitations and protections of trade secrets? I find the point of another company having the same product without breeching any confidentiality violations very interesting. From the example provided in the lectures, it is a very rare situation th... |
In forum Consultants and Legal Basics |
3 years ago |
RE: Confidentiality Agreements As discussed in the lectures, the CDA and NDA will have all the basic parts that a contract would have. These would ofcourse include all the basics for confidentiality, trade secrets and information, ... |
In forum Consultants and Legal Basics |
3 years ago |
RE: Project management I believe the best way to think about the Design Development Plan is as a complete lay out of blueprint of the project. The basic documentation and planning such as the Gantt chart (prelimary gantt ch... |
3 years ago | |
RE: For those that work in a matrix based organization: I work at a matrix organization based medical device company and I can see how it could be over-whelming being on multiple projects, especially for the more experienced positions with additional respo... |
3 years ago | |
RE: Desicion made by one person I believe that even though there is one official person making the decisions, they still have their personal assistance from other professionals around them that are providing vital insight and advice... |
3 years ago | |
RE: Risk Management Process While I have not had direct experience with risk management or the scenarios you mentioned above, I think the examples in the lecture (using a scalpel for cutting) were great on depicting what kind of... |
In forum Risk Analysis for Medical Devices |
3 years ago |
RE: Getting Everyone's Input in Risk Management Meetings I currently work at a medical device development company in the industry and am going to be attending my first risk management meeting in the near weeks. However, I will say that meetings as important... |
In forum Risk Analysis for Medical Devices |
3 years ago |
RE: US FDA vs EU MDR Risk management This is interesting because based on the lecture, I thought that ISO 13485 was the medical device ISO standard, meaning that USA also follows this standard. I believe that Europe also has their versio... |
In forum Risk Analysis for Medical Devices |
3 years ago |