Delta Cleanroom (“Delta Cleanroom”), as a specialist in the pharmaceutical industry, provides design and qualification services in accordance with the principles of risk management, EU GMP guidelines, WHO and US Food and Drug Administration regulations and standards, in relation to industrial systems, and in order to ensure compliance with current standards and requirements legislation.
The development of design and technical documentation includes:
Our company provides a service for the development of a Containment strategy and Risk Assessment in the pharmaceutical industry, ensuring process reliability, product and personnel protection, fully in accordance with GMP standards and ICH Q9 risk management guidelines.
