
Sobre este pódcast
Hello Combi-Nation! Our industry fee complicated sometimes. Drugs, devices, clinical trials, submissions, sterilization validation, design control, risk management, market access reimbursement, the list goes on. My name is Subhi Saadeh. I've spent over a decade in medical device, pharma, and combination product development. My goal is mastery, so this podcast is to ask questions I have to people who may have the answers. Whether you're background is Pharma, Device or both, I invite you to…
265 episodios · Ciencias de la vida
Let's Combinate - Pharma + Medical Devices with Subhi Saadeh
Sobre este pódcast
Hello Combi-Nation! Our industry fee complicated sometimes. Drugs, devices, clinical trials, submissions, sterilization validation, design control, risk management, market access reimbursement, the list goes on. My name is Subhi Saadeh. I've spent over a decade in medical device, pharma, and combination product development. My goal is mastery, so this podcast is to ask questions I have to people who may have the answers. Whether you're background is Pharma, Device or both, I invite you to…
Episodios recientes
- 257 - 21 CFR Part 4 Explained: CGMP Requirements for Combination Products5 oct · 13 min
- 256 - The New FDA Inspection Playbook: Where to Start with QMSR28 sept · 9 min
- 255 - Audit Interview Techniques: How Good Auditors Get Better Evidence21 sept · 12 min
- 254 - Saying No Is the Easy Part of Quality13 sept · 12 min
- 253 - FDA Is Making Big Changes to Its Inspection Approach7 sept · 46 min
- 252 - Acceptance Sampling Fundamentals: AQL, Attributes vs Variables, and Risk (OC Curves)31 ago · 13 min
- 251 - The Future of Drug Delivery: Orals, Injectables, Sustainability & Device Strategy24 ago · 49 min
- I'm Changing The Podcast18 ago · 3 min
- 250 - PIC/S PI 006-4 (2026): What Changed in Qualification & Validation?12 ago · 11 min
- 249 - The Best Audit Advice Nobody Told Me5 ago · 14 min