# About SteriQual Solutions

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

Canonical: https://steriqualsolutions.com/about-us

## Specialized expertise in critical environment compliance

Founded in Ahmedabad, SteriQual Solutions Pvt. Ltd. was established to address the critical need for robust, technically sound compliance and contamination control strategies in high-precision industries.

With a foundation built on advanced postgraduate microbiology credentials and over 16 years of hands-on quality control and aseptic processing experience, we deliver precision-driven qualification, validation and contamination control strategies. Our technical framework is backed by firsthand experience managing facility and system audits from the USFDA, EMA and INVIMA.

We also provide deep-dive expertise in microbial excursion investigations, operational deviations, aseptic processing simulation (APS) failures and out-of-specification (OOS) results, with robust root-cause identification and CAPA implementation.

## Areas of focus

- Pharmaceutical and biopharmaceutical sectors
- Semiconductor and microelectronics manufacturing
- Controlled cleanroom environments
- Sterile and depyrogenated consumables supply chain

## Vision

To be the most trusted quality partner for cleanrooms worldwide, known for simple compliance and accurate data.

## Mission

To protect product quality and patient safety by providing premium sterile supplies, clear facility qualifications, and fast expert solutions for contamination issues.

## Core values

- **True science**: every solution, protocol and failure check is based on clear facts and proven microbiology principles.
- **Global standards**: facilities kept ready for strict international audits like USFDA, EMA and current GMP guidelines.
- **Practical support**: easy-to-use workflows, protocols and reports that fit daily plant routines.
- **Tailored solutions**: customized solutions beyond the predefined checklist.

## Leadership

### Mehul Panchal

Principal Consultant. Postgraduate, Microbiology, 16+ years (QC microbiology & aseptic processing).

Advanced postgraduate credentials in microbiology with over 16 years of core industrial experience in quality control microbiology and aseptic processing techniques. A proven track record managing regulatory audits from the USFDA, EMA and INVIMA, with specialized expertise in resolving microbial excursions, deviations, APS failures and OOS results.

Expertise: Microbial excursions, Deviations, APS failures, OOS results.

### Dharmesh Prajapati

Consultant, Instrumentation & Equipment Compliance. B.E. Instrumentation, 12 years (Pharmaceutical equipment engineering).

A B.E. in Instrumentation with 12 years of specialized engineering experience focused on pharmaceutical industry equipment. Provides expert oversight for hardware qualification, automation validation and instrument calibration alignment, so your critical systems fit modern production requirements.

Expertise: Hardware qualification, Automation validation, Instrument calibration.