Meet our Subject Matter Experts

Adam Saltman, PhD, MD

Chief Medical Officer

Clinical, FDA, Product Development, Regulatory

Adrian Keene

Associate VP, Global Biological Safety & Validation and EMEA Consulting Services

Biological Safety, Clinical, EU IVDR, EU MDR, Regulatory

Áine Mary Duffy, BSc (Hons), PhD

Clinical & Regulatory Operations Manager

Clinical, EU MDR, FDA, Medical Writing, Regulatory

Andrea Perciaccante

Analysis Leader

Market Research, Quality, Regulatory

Ariadna Navarro, PhD

Senior Strategy Consultant

Clinical, EU IVDR, EU MDR, IVD, Medical Writing, Quality, Regulatory

Aurélie San Juan, MSc, PhD

Principal Medical Writer, Regulatory

EU MDR, Medical Writing, Regulatory

Beverly Lundell, MSc, PhD

Scientific Director, Custom Studies

Biocompatibility, Biological Safety, FDA, Interventional & Surgical Research, Preclinical, Product Development, Regulatory

Brandon Woll, MBA

Principal Strategy Consultant

Director, FDA, Preclinical, Product Development, Quality, Regulatory, Validation

Britt Jones

Group Manager, Chemistry and Package Testing

FDA, Microbiology, Preclinical, Regulatory

Britta Rupp, PhD

Clinical Strategy Consultant

Clinical, Medical Writing, Regulatory

Carla Wiese

Carla M. Wiese, BS-Mech Eng

Principal Strategy Consultant, Regulatory

FDA, Product Development, Regulatory

Caroline Guidicelli

Caroline Guidicelli, MSc, MEng

Principal Medical Writer

EU MDR, Medical Writing, Regulatory

Catherine Tremolieres, DVM

Manager, Biological Safety & Validation Consulting Services, Europe

Biocompatibility, Biological Safety, Chemical Characterization, EU MDR, FDA, Regulatory, Toxicology

Chris Mullin

Chris Mullin, MS

Director, Global Strategy Services

Biostatistics, Clinical, FDA, Product Development, Regulatory

Christèle East, PhD

Christèle East, PhD

Senior Regulatory Consultant, IVD

Clinical, EU IVDR, FDA, IVD, Medical Writing, Quality, Regulatory

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