KINGROCK Overview

Focus on medical technology services
Create a new mode of project comprehensive management

KINGROCK was established in January 2020 with its headquarters in Guangzhou, China. We have been deeply involved in the field of medical device service for decades. We bring together an international expert team with extensive industrial experience, equipped with laboratories built according to the highest quality system requirements and international standards. we always consider client services as our core value with professional technical services for the whole industrial chain of medical devices.

We provide medical device manufacturers with unparalleled top-quality services, including biocompatibility testing, preclinical performance testing in vivo, clinical research, international registration consultancy, customized quality and customized trainings, etc to help them get their products into the market in the shortest time and in the most cost effective way.

Corporate Culture

Vision

Become a reliable, professional and authoritative international third-party service platform
Mission

We are committed to bringing safe, effective and compliant medical devices to every patient in the world.
Values

Professional&Pragmatic, Scientific&Rigovous, Professional&Efficient, Constantly Perfecting.
Objective

To be the leading 3rd-party platform of medical devices in APAC.

Milestones

2020

KINGROCK was founded in 2020.

Headquarter and Preclinical testing lab in Guangzhou.

Regulatory Consultancy & Clinical offices in Beijing and Shanghai China.

We built the first comprehensive service platform that integrating the GLP laboratory, registration consultation, clinical research and training services of high-end medical devices in south China, we also carry out cross functional collaboration.

Professional and efficient overall solutions for medical device companies to speed up market access.

Leadership

Key management team members of KINGROCK originate from international notified body, well-known CRO companies and medical device companies, the abundant experience in each stage of clinical trials and observational studies will help to provide customers with comprehensive professional services from strategy development, protocol design, project operation, data management and analysis to registration. This will optimize project management operations, raising efficiency and minimizing risks during trials operation.