Meet our Subject Matter Experts

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

Cayla Ruch, PhD, DABT

Biocompatibility, Toxicology

Céline Furne, PhD

Biological Safety Scientist

Biological Safety

Chad Reiter, PhD, DABT

Biocompatibility, Toxicology

Chikako Kitayama, PhD, DABT

Senior Biological Safety Scientist

Biocompatibility, Biological Safety

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

Christophe Van der Linden

Executive Director Marketing Insights & Consulting

Market Research

Cindy Dingee, DVM

Histopathology Operations Manager and Veterinary Pathologist

Biocompatibility, Biological Safety, FDA, Preclinical, Regulatory

Corey Leet

Director, Regional Preclinical and In-Vivo Biocompatibility Operations

Director, FDA, Interventional & Surgical Research, Preclinical

Corie Diaz

Corie Diaz, BA, MBA

Global Director, Clinical Operations

Clinical, Regulatory

Crystal Jurkiewicz, BS, MS, DABT

Biocompatibility, Biological Safety, Toxicology

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