• APC – YOUR MEDICAL DEVICE CRO

    Our Vision

    “BEING THE BEST IN CLASS DRIVER OF ACCELERATING THE DEVELOPMENT OF SAFE AND PERFORMING MEDICAL DEVICES TO IMPROVE THE HEALTH OF PATIENTS ALL OVER THE WORLD”

  • APC – YOUR RELIABLE PARTNER

    Our Mission

    "LIVING DAY-TO-DAY AN UNCOMPROMISING DEDICATION TO CLINICAL SAFETY AND PERFORMANCE"

  • APC – YOUR PARTNER TO SUCCESS

    Our Promise

    "WE PROMISE QUALITY RESULTS IN TIME AND BUDGET" ​

APC MEETS THE CHALLENGE OF THE NEW EU REGULATION 2017/745 (MDR)

Facing the challenge of increased necessity of clinical evidence targeting any Medical Device. We are your reliable partner in the conception, creation and bring up to date of your clinical records all the way through the entire product life cycle. You won’t miss a single stage in the documentation of your product. From the first outline and the concept to the market phase of your Medical Device APC is familiar with the critical clinical documentation necessary being successful all along the Life Cycle of your Medical Device. APC prevents you from missing the Creation and Updating of mandatory Clinical Documents

QUALITY MANAGEMENT

...Ensures that an organization, product or service is consistent... Updating your QM System means....

MEDICAL WRITING

Requirements and Proceedings for a Clinical Evaluation using Clinical Data Starting the Process: How we begin...

CLINICAL INVESTIGATIONS & PMCF STUDIES

Clinical Investigation - full service from start to completition or selected services...

Our Partner