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ih37
@ih37
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Joined: Sep 14, 2018
Topics: 0 / Replies: 78
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RE: Risk Identification

My company manufactures a blood-based infusion product that is currently undergoing its clinical phase in trials, so it is common for errors to occur ...

6 years ago
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RE: Manage Risk

The first part of risk management, as mentioned, is to assess all the potential threats of a device by formulating a list of risks associated with its...

6 years ago
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RE: Discussion Topic: Risk Management, Risk Analysis

The major ISO for risk management is ISO 14971, which is enforced onto medical device companies as a means of preventing or mitigating the hazards ass...

6 years ago
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RE: a successful validation process

A proper validation process should revolve around the patient by ensuring that the medical device under development meets the user's needs. An import...

6 years ago
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RE: Deviations That Occurs During Verification

The clinical research company I work for carries out cell therapy in that T-cells are taken from a patient's blood, which are then amplified via addit...

6 years ago
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RE: Design Review Meetings

The company that I work for carries out clinical research involving the processing of auto/allogeneic cell-based products for therapeutic purposes. E...

6 years ago
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RE: Factors to Consider While making Gantt Chart

I have not worked with Gantt charts in industry, though I have during my senior design project in developing a neuro-prosthetic arm. The first factor...

6 years ago
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RE: Design Transfer and Challenges

The design transfer process aims to translate the design of a medical device into a production procedure in which the manufactured device can fully ma...

6 years ago
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RE: Discussion Topic: Supplemental on DHF and DMR

Design controls are certainly enforced throughout the development process of medical devices in the EU, the real question is whether or not they are s...

6 years ago
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RE: Clinical Studies

An advantage to clinical testing is being able to come up with a breakthrough medical device/technique that treats many patients to unique illnesses w...

6 years ago
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RE: Informed consent: What if Henrietta Lacks checked No for research use?

The debate as to whether or not informed-consent should remain a law or be defunct really comes down to the pros and cons. If Henrietta Lacks had the...

6 years ago
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RE: Discussion Topic: Having a "clinical background"

When analyzing the qualifications for a CRA position, the first factor that comes to mind is what type of clinical product is being put through trial?...

6 years ago
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RE: Discussion Topic: Mission and Vision statements

A vision statement is a company's envisionment of the future regarding where they hope to stand and what they hope to have accomplished while a missio...

6 years ago
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RE: Discussion Topic: The Fifth "P" of Marketing

The participation aspect of marketing (the fifth "P") seems to have gained recognition over the past two decades due to the excessive tactic of "push ...

6 years ago
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RE: Discussion Topic: Emotional Intelligence and its affect on sales

Emotional Intelligence (EI) is the level of intelligence one possesses when analyzing the emotional state or condition that another individual is in s...

6 years ago
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