Preparing Biocompatibility Risk Assessments for International Registration

AATCC TM 100-2019: Assessment of & What It Means for Medical Textiles

ANSI/AAMI ST72:2019 update & key learnings on BET

ISO 11607 & MDR Impacts on Package Testing & Validation

ISO 10993-18 Updates: What You Need to Know

Stop Letting GLP Stunt Your Chemistry Studies

WuXi Medical Device Testing Doubles Chemistry Capacity

Are you MDR ready? Let WuXi AppTec be your guide at BIOMEDevice in San Jose

WuXi AppTec Welcomes Sherry Parker, Ph.D., as Senior Director of Regulatory Toxicology

Preparing for MDR: Don’t Forget about Class I Reusable Devices

MDR & ISO 10993-1: How to Navigate Preclinical Device Testing

ISO 10993-1: The Importance of Chemical Characterization

A Regulatory Consultant's Guide to ISO 10993 Updates Webinar

Our All-Inclusive Approach to Microbial Identification

Environmental Monitoring Supports a Risk-Based Approach to Manufacturing Control

WuXi AppTec to Exhibit at DeviceTalks West, Costa Mesa, California

Radiation Sterilization: Verifying Dose Survivors

Radiation Sterilization: Product Bioburden and Verification Dose

Product Adoption for Sterilization Validation

Poor Extraction Methods Can Impact Study Results

wuxi apptec to exhibit at devicetalks boston

WuXi AppTec Technical Experts at the American Association of Tissue Banks Expo, Booth #49

Register Now for the PDA Chapter Dinner and Biocompatibility Presentation

WuXi AppTec to Present Case Study: Enhancing Biocompatibility Testing via Device-Specific Chemical Analysis

Designing Disinfectant Efficacy Studies for All of Your Facility Locations

WuXi AppTec Now Offers Dual Route Subchronic Toxicity Test

Cleaning Validations and Process Robustness: How to Build a Study Design

Scientific Principles in Practice: Study Directors’ Participation is Vital for Good Laboratory Practices

Limited Space, Register Now for two SEMINARS. day 1: ISO 10993 Case Studies and day 2: dissecting the changes of iso 10993 part 18.

Facility Disinfectant Efficacy Studies – Complex, Resource Demanding and Extremely Necessary

One-Stop Shop for Tissue-Based Products

Helping Manufacturers Understand Product Bioburden Before Dose Setting

WuXi AppTec Attends FDA Workshop “Accreditation Scheme for Conformity Assessment (ASCA) of Medical Devices to FDA-Recognized Standards"

Important to Address the Stacked Effects of Soil Accumulation on Medical Devices

WuXi AppTec Names Tim Drain as Director of Sales

A Risk-Based Approach to Medical Device Testing Starts with Extractables and Leachables

WuXi AppTec Names Mark Cunningham as Senior Director of Science and Technology

WuXi AppTec Offers PTT Testing with BFT II Analysis

WuXi AppTec to Exhibit at DeviceTalks Minnesota

Wuxi AppTec Provides Wide Range of Consulting Services

WuXi AppTec Names former FDA Commissioner’s fellow as a Senior Scientific Director

Q1 Productions 8th Annual Packaging Conference

WuXi AppTec Joins Industry Leaders on Extractables & Leachables at E&L USA

The Changing Landscape Of Medtech Regulation