Discussions – Page 2 – INDiE Med Tech

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Holly

New FDA Guidance Documents

Holly replied 7 months, 2 weeks ago 2 Members · 2 Replies

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Joe

P1/P2 Values RIsk Management

Niki replied 8 months ago 3 Members · 3 Replies

Risk Management
Holly

BDR or Pre-Sub?

Holly replied 8 months, 1 week ago 1 Member · 0 Replies

Regulatory
Michelle

QMSR Transition: Medical Device File vs. DMR/DHF

Jude replied 9 months, 1 week ago 4 Members · 10 Replies

Quality
Peter

Networking

Holly replied 9 months, 1 week ago 2 Members · 1 Reply

Marketing and Business Development
Holly

FutureReady: MedTech Live – Episode 01 – Consulting

Holly replied 9 months, 3 weeks ago 1 Member · 0 Replies

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Jude

Malaysia is now a MDSAP member

Holly replied 11 months ago 2 Members · 1 Reply

Regulatory
Nicholas

Now hiring at MEDIcept – Sr. Regulatory Consultant

Nicholas replied 11 months, 1 week ago 1 Member · 0 Replies

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Daria

ISO 10993-1:2025

Holly replied 11 months, 2 weeks ago 2 Members · 1 Reply

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Amie

Medical device?

Melissa replied 11 months, 2 weeks ago 3 Members · 2 Replies

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Theresa

Event Announcement for this amazing forum!

Niki replied 11 months, 3 weeks ago 4 Members · 3 Replies

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Nicholas

Available Cyber work

Peter replied 11 months, 3 weeks ago 3 Members · 3 Replies

Consulting
Amie

Definition of “clinical investigation”

Amie replied 11 months, 3 weeks ago 2 Members · 4 Replies

Clinical Evidence
Niki

Real-time AE Reporting

Holly replied 12 months ago 2 Members · 1 Reply

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Holly

How to manage time with multiple clients?

Holly replied 12 months ago 2 Members · 2 Replies

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