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Pharma IQ

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Articles

Career Spotlight: Pharma Regulatory Affairs

Contributor: Pharma IQ
Posted: 9/1/2010

Career Spotlight: Pharma Regulatory Affairs - Pharma IQ

Pharma regulatory affairs professionals play an essential role in ensuring all pharmaceutical products comply with regulations governing the industry. Those working in pharma regulatory affairs jobs not only work in the initial application phase for a new or generic drug, but... Full Article

 
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Videos

The Human Factor’s Engineering Process in the Development of Medical Device Software

Contributor: Edmond Israelski
Posted: 8/27/2010

The Human Factor’s Engineering Process in the Development of Medical Device Software - Edmond Israelski

View this presentation to find out about integrating human factors engineering into medical devices to make them safe, effective and efficient to use, and the regulations for the human factors engineering process. Presented by Dr. Edmond W. Israelski, Hum... Full Video

 
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Podcasts

What's Next for the Medical Devices Market? Regulatory Changes

Contributor: Pharma IQ
Posted: 8/26/2010

What's Next for the Medical Devices Market? Regulatory Changes - Pharma IQ

With the increasing evidence-based medicine politics, the medical device market is changing. In this interview with Helen Winsor from Pharma IQ, Danielle Giroud, Founder of the World Medical Device Organisation, offers her viewpoint on the direction the market is moving in. She discus... Full Podcast

 
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What documents are required for ANDA submission and how does the process work? Are the any good online guides?

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hi i was asking do i need a wrirten permision from you to write about your site or the news in your sit but i guide people to your site to register in the...

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How effective will the use of monoclonal antibody-based approaches be within asthma & COPD drug development and future commercial pipelines?

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How are GSK making leaps and strides in biopharma?

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What pharma/biotech companies are making headway by using technology in clinical trials and who is spearheading this?

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What documents are required for ANDA submission and how does the process work?

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