COMPANY PROFILE

QPRO is a Project Management company in the fields of:
Quality Assurance, Quality Engineering, Regulatory Affairs, and Technology Transfer.
QPRO offers services related to the Pharmaceutical, Medical Devices, API and Chemical industries by utilizing the expertise of individuals with many years of industrial and academic experience.
The aim of the company is to teach, develop, assist, plan, train, support, the Pharmaceutical and Medical Devices companies enter the global market through assistance in the regulatory and technological fields.

The following is QPRO's area of expertise:

In the technological field:
Process development, Scale-up, Process improvement, Technology transfer,
Production facilities planning, Analytical methods development.

In the regulatory field:
GMP compliance, Planning of pharmaceutical water systems, SOP’s preparation, CMC section of registration files and Drug Master Files, Pre-approval inspections (PAI), Training, , Process validation, Analytical methods validation, Validation Master Files preparation. ISO 9001:2000 compliance programs including ISO 13485 (Medical Devices), ISO 90003 (Computers), CE and UL (Safety).