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shreya
@shreya
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Joined: Sep 9, 2025
Last seen: May 3, 2026
Topics: 0 / Replies: 69
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RE: Developmental Life Cycles

One thing I’ve noticed is that the right developmental life cycle often depends less on the industry and more on how mature the requirements and risk ...

3 months ago
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RE: The Nine Points of Design Control and How to Effictively Use and Understand Them.

One thing I’d add is that a strong DHF isn’t just about having all the right documents, it's also about showing clear traceability and change control ...

3 months ago
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RE: Product Life Cycle - Impacts & Management

One additional factor that influences a medical device’s product life cycle is how well design transfer and manufacturing readiness are handled early ...

3 months ago
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RE: Managing Scope and Stakeholder Expectations

I think the threshold for moving from repeated verification iterations to a formal scope change should be based less on the number of failures and mor...

4 months ago
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RE: Pre-market Approval (PMA) vs. 510(k)

One angle I haven’t seen discussed yet is how much the intended use and claims of a device can influence whether a company ends up on the PMA or 510(k...

4 months ago
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RE: Relationship between the FDA and Project Managers

I think one of the most effective ways for project managers to work within the FDA’s constraints is by involving regulatory considerations early on, i...

4 months ago
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RE: How can a project manager excel in the Biomedical field?

A lot of great points here focus on communication, prioritization, and technical awareness, but one skill I think ties all of those together is decisi...

4 months ago
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RE: The Cross Disciplinary Skills Needed in a Project Manager

One thing I haven’t seen discussed yet is how the best background for a medical device PM might actually depend on what stage of the product lifecycle...

4 months ago
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RE: Team Conflict with Project Manager

Another angle is that ongoing conflict can sometimes point to a process issue rather than a people issue. If a project manager and a highly skilled te...

4 months ago
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RE: Are We Over-Relying on FMEAs?

One issue I see with depending too much on FMEAs is that they are predicated on the idea that failures occur one component at a time in predictable wa...

6 months ago
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RE: Can Risk Really Be Eliminated — or Only Managed?

One thing that often gets overlooked is that risk isn’t just tied to the device design but it’s tied to the patient using it. Two people with the same...

6 months ago
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RE: When Mitigation Becomes Its Own Risk!

Sometimes a mitigation doesn’t make the product safer overall, it just transfers the risk to a different user group, workflow, or failure mode. For ex...

6 months ago
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RE: Updating documentation or information overload?

Everyone’s shared great technical solutions, but another issue behind documentation fatigue is how people interact with the process, not just the tool...

6 months ago
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RE: When Design Controls Fail — The DePuy Hip Recall

Everyone’s made great points about prediction limits and company oversight. Another major gap is that verification and validation don’t really reflect...

6 months ago
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RE: Can Verification Cause a Tragedy?

While many have raised valid points about adaptive algorithms and overconfidence in structured systems, I think a modern “Therac moment” could result ...

6 months ago
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