# SteriQual Solutions Pvt. Ltd.

> Ahmedabad-based GMP consulting: cleanroom and equipment qualification, CSV, contamination control, mock audits, training and sterile lab consumables.

Canonical: https://steriqualsolutions.com/

## Your partner in compliance

GMP technical consultation, qualification solutions and training. SteriQual provides cleanroom qualification for pharmaceutical and semiconductor industries, equipment qualification and CSV, GMP consultation, mock audits, and robust contamination control strategies.

## Regulatory audits faced and defended

- **USFDA**: U.S. Food and Drug Administration (United States)
- **EMA**: European Medicines Agency (European Union)
- **INVIMA**: Instituto Nacional de Vigilancia de Medicamentos y Alimentos (Colombia)

## Work aligned with

- **ISO 14644-1** (Cleanroom classification): Classifies air cleanliness by the concentration of airborne particles.
- **ISO 14644-3** (Cleanroom test methods): Test methods for airflow, pressure, filter leaks, recovery and containment.
- **USFDA cGMP** (United States): 21 CFR Parts 210 and 211 for drug manufacturing, and Part 11 for electronic records.
- **EU GMP** (European Union): EudraLex Volume 4, including Annex 1 for sterile medicinal products.
- **PIC/S GMP** (International): The GMP guide shared by inspectorates of the Pharmaceutical Inspection Co-operation Scheme.
- **Schedule M** (India): GMP requirements under the Drugs and Cosmetics Act, 1940 and its Rules.

## Where microbiology expertise meets rigorous GMP

Based in Ahmedabad, SteriQual Solutions Pvt. Ltd. provides specialized technical consulting for pharmaceutical, semiconductor and controlled cleanroom environments. We leverage more than 16 years of industrial QC microbiology experience to design robust facility qualifications and audit-ready contamination control workflows.

## Service areas

- [Pharmaceutical GMP & Investigation Services](https://steriqualsolutions.com/services.md): Comprehensive compliance, risk management and validation frameworks for sterile and non-sterile drug manufacturing facilities.
- [Precision Cleanroom Qualification & Testing](https://steriqualsolutions.com/services.md): Advanced environmental monitoring, structural integrity assessments and particle dynamic testing, tailored to meet stringent semiconductor manufacturing standards.
- [Laboratory Consumables and Equipment](https://steriqualsolutions.com/products.md): Supply of high-calibre sterile and depyrogenated consumables, and laboratory testing instruments tailored for pharmaceutical QC environments.

## Our approach

- **Microbiology-driven**: 16+ years of core industrial QC expertise to identify, isolate and mitigate cleanroom contamination vectors.
- **Audit-ready blueprints**: rigorous validation protocols and computer system validation frameworks shaped around global regulatory expectations.
- **Data-reliability focused**: traceably documented procedures and training structures that eliminate laboratory subjectivity and human error.

## Contact

- Office: SteriQual Solutions Private Limited, 504 Yash Aqua, Vijay Char Rasta, Navrangpura, Ahmedabad 380009, Gujarat, India
- Email: info@steriqualsolutions.com
- Phone: +91 90160 57338, +91 88664 95014
- Enquiry form: https://steriqualsolutions.com/contact-us

## Pages

- [Home](https://steriqualsolutions.com/index.md)
- [About Us](https://steriqualsolutions.com/about-us.md)
- [Services](https://steriqualsolutions.com/services.md)
- [Laboratory Consumables and Equipment](https://steriqualsolutions.com/products.md)
- [Contact Us](https://steriqualsolutions.com/contact-us.md)
- [Privacy Policy](https://steriqualsolutions.com/privacy-policy.md)
- [Terms of Use](https://steriqualsolutions.com/terms-of-use.md)