In the pharmaceutical industry, contamination control is paramount, as it directly impacts human health and well-being.

At Aastha, we Design and Build Pharmaceutical Cleanrooms with meticulous attention to detail, strictly adhering to all relevant guidelines and regulatory requirements.

With our proven expertise, technical know-how, and years of experience, we have earned the trust of leading pharmaceutical companies in India and abroad. Many of them continue to collaborate with us, entrusting Aastha with the development of their state-of-the-art cleanroom facilities.

Pharmaceutical Cleanrooms are required to comply with stringent international standards to ensure product quality and patient safety.

• ISO 14644 Standards
  Cleanrooms must meet the cleanliness classifications defined in ISO 14644 (Classes ISO 1–9), covering critical parameters such as particle count, temperature, pressure, and humidity.

• GMP (Good Manufacturing Practice)
  In addition to ISO standards, pharmaceutical cleanrooms must also comply with GMP guidelines, which are designed to minimize risks during the production of pharmaceutical products, including medicines, medical devices, and related equipment.

Together, ISO 14644 and GMP form the foundation for safe, compliant, and efficient cleanroom operations in the pharmaceutical sector.