Medical Device Courses | ppp23 | Mentions https://medicaldevicecourses.com/members/ppp23/activity/mentions/ Activity feed mentioning ppp23. Fri, 24 Apr 2026 22:39:12 -0400 https://buddypress.org/?v= en-US 30 hourly 2 43b7ad8bc07f65053a577609e06668c0 thuytienlecao replied to the topic "What FDA Looks For In A Design Control System ?" - https://medicaldevicecourses.com/activity/p/13859/ Wed, 15 May 2019 17:08:52 -0400 @ppp23: if you are asking about what it is, it stated on that document that “Design output means the results of a design effort at each design phase and at the end of the total design effort. The finished design…   Read more»

]]> 0ef94e2881e0a428d83671e1e3717d97 alexandrabuga replied to the topic "Clinical Trial Roles" - https://medicaldevicecourses.com/activity/p/13662/ Wed, 15 May 2019 17:07:02 -0400 If it was a sponsored clinical trial, I would be the sponsor as @ppp23 and @mark mentions, the sponsor selects the PI, prepares and submits clinical trial application and amendments to the appropriate regulatory agencies and ensures that the clinical…   Read more»

]]> 2d6f7659b0381b77d9a5f8bc72158a38 thuytienlecao replied to the topic "Discussion Topic: Emotional Intelligence and its affect on sales" - https://medicaldevicecourses.com/activity/p/13628/ Wed, 15 May 2019 17:06:42 -0400 I agreed with previous posts (from @aaq2 & @ppp23 …) about the definition of EI, the importance of EI in marketing and Kidwell’s paper. I also think that EI is essential in marketing However, I would like to add a…   Read more»

]]> 453efae2d83db2df5f138a797357ff95 thuytienlecao replied to the topic What FDA Looks For In A Design Control System ? in the forum Introduction to Design Controls https://medicaldevicecourses.com/activity/p/4865/ Sun, 05 Nov 2017 03:27:08 -0500 @ppp23: if you are asking about what it is, it stated on that document that “Design output means the results of a design effort at each design phase and at the end of the total design effort. The finished design output is the basis for the device master record. The total finished design output consists of the device, its packaging and labeling,…[Read more]

]]> 0 c0cd1f35d191d9ad5542098b2eceb6ea alexandrabuga replied to the topic Clinical Trial Roles in the forum Clinical Research Basics https://medicaldevicecourses.com/activity/p/4383/ Tue, 24 Oct 2017 23:59:07 -0400 If it was a sponsored clinical trial, I would be the sponsor as @ppp23 and @mark mentions, the sponsor selects the PI, prepares and submits clinical trial application and amendments to the appropriate regulatory agencies and ensures that the clinical study is conducted in accordance with Good Clinical Practices (GCP). I think its exciting to have…[Read more]

]]> 0 1927b7c12533b02eeed102904ef3587b thuytienlecao replied to the topic Discussion Topic: Emotional Intelligence and its affect on sales in the forum Marketing and Sales https://medicaldevicecourses.com/activity/p/4350/ Mon, 23 Oct 2017 02:48:42 -0400 I agreed with previous posts (from @aaq2 & @ppp23 …) about the definition of EI, the importance of EI in marketing and Kidwell’s paper. I also think that EI is essential in marketing
However, I would like to add a few points about the “cons” of EI that haven’t been mentioned. I believe these points are not “negative” but they are something worth…[Read more]

]]> 0 2d6a22b5ef9f3ddf1d69cdf205f1e267 rd389 replied to the topic Failure's of Pre-Clinical / Clinical Research in the forum Pre-clinical Device Development https://medicaldevicecourses.com/activity/p/3530/ Mon, 25 Sep 2017 13:23:09 -0400 1. Why was a need to overdose animals?
2. What measures were taken to avoid future overdosing to animals?
3. How were the dead animals disposed?
4. Any care was taken during disposing, considering bio hazards?

Sorry to reply to you guys (@ppp23 @scott) so late. So, I deal with the samples that are taken from these monkeys or other animals,…[Read more]

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