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mduru replied to the topic "FDA Consultants in medical devices projects" – 4 years, 8 months ago
I agree with you Jafar, I think it’s a good idea to have RA (Regulatory Affairs) in the first meeting as well. Having input from RA could help prevent issues in the future of the project. I personally know of… Read more»
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mduru posted a new topic "Ethics and Regulation of Medical Device Development and Manufacturing in Times of Crisis" – 4 years, 9 months ago
During the COVID19 pandemic we’ve seen significant shift of resources in many industries. The medical device industry was one of the industries that felt this shift the strongest. Some approvals were fast tracked by regulators while some others put on… Read more»
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mduru replied to the topic "Discussion Topic: Covid19 and medical devices" – 4 years, 9 months ago
COVID19 has in some ways helped and continue to help use in our methods and technology. As mentions in previous posts, companies and people who originally had nothing to do with the medical industry have now gotten involved in the… Read more»
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mduru replied to the topic "The Advantages and Disadvantages of Being Overqualified" – 4 years, 9 months ago
I think it really depends on what you want and company culture as well as your management. Here are a few advantages I see in being over qualified: Advantage over others who are seeking the same salary and position. Opportunities… Read more»
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mduru became a registered member 4 years, 9 months ago