About Techval
Your trusted partner in pharma validation, digital transformation, and audit compliance.
About Techval™ Services
We Expertise In
In the modern pharmaceutical and healthcare landscape, regulatory compliance, validation, and quality assurance are not just requirements—they’re the backbone of trust, safety, and operational excellence. Techval™ Services stands as an independent and highly specialized validation and qualification partner dedicated to supporting the pharmaceutical (injectable, OSD, API), biotechnology, medical device, and healthcare sectors with comprehensive and reliable solutions.
Who We Are
Techval™ Services is a trusted name in the field of validation and qualification services, known for its technical expertise, precision-driven execution, and commitment to compliance. We deliver end-to-end solutions that empower businesses to meet global regulatory standards while enhancing product quality, safety, and system reliability.
Our team is composed of experienced validation engineers, QA specialists, and compliance experts who have deep domain knowledge across regulated environments. Whether you’re setting up a new facility, qualifying utilities and equipment, or ensuring documentation readiness for audits, Techval™ ensures your systems are fully compliant, efficient, and audit-ready.
Our Core Expertise
At Techval™, we offer a complete range of validation and qualification solutions covering every critical aspect of your operations, including:
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Equipment Qualification (IQ, OQ, PQ)
Ensuring your equipment is installed, operated, and performing according to defined specifications and regulatory expectations. -
Utility and HVAC Validation
Comprehensive testing and documentation to confirm cleanroom, HVAC, and utility systems meet regulatory standards for controlled environments. -
Computer System Validation (CSV)
Robust validation of software systems and automated processes in compliance with 21 CFR Part 11, Annex 11, and other global guidelines. -
Process Validation
Scientific and data-driven validation to ensure your manufacturing processes consistently produce quality products. -
Cleaning Validation
Meticulous evaluation and documentation of cleaning processes to prevent cross-contamination and ensure product safety. -
Thermal Mapping & Qualification
Precision-driven temperature and humidity mapping of critical storage and manufacturing areas, using advanced calibrated instruments. -
Environmental Monitoring & Qualification
Establishing and validating monitoring systems that maintain consistent control over cleanroom and process environments.
Our Mission
At Techval™ Services, our mission is to empower pharmaceutical, biotech, and healthcare companies with the confidence that their systems, facilities, and documentation not only comply with regulations but also achieve operational excellence.
We strictly align our services with global regulatory standards such as:
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US FDA (Food and Drug Administration)
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EU-GMP (European Good Manufacturing Practice)
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WHO (World Health Organization)
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MHRA (Medicines and Healthcare products Regulatory Agency)
Our commitment is simple: to provide regulatory-driven, technically precise, and reliable validation solutions that withstand any audit and contribute to long-term business sustainability.
Why Choose Techval™ Services
Choosing Techval™ means choosing trust, expertise, and quality. Here’s why leading pharma and healthcare organizations partner with us:
1. Regulatory Expertise
Our team stays continuously updated with the latest global validation guidelines to ensure every project is aligned with FDA, EU-GMP, WHO, and MHRA expectations.
2. End-to-End Solutions
From initial protocol design to execution, reporting, and documentation, we manage the entire validation lifecycle with precision and accountability.
3. Experienced Professionals
Each member of the Techval™ team brings extensive hands-on experience in pharma validation, qualification, and regulatory compliance, ensuring the highest standards of work.
4. Quality and Compliance Focus
We believe validation isn’t just about passing audits—it’s about building systems that deliver consistent quality and performance.
5. Audit-Ready Documentation
Our reports, templates, and protocols are structured to meet and exceed international regulatory expectations, ensuring complete audit readiness.
6. Customized Solutions
We understand that every facility and process is unique. That’s why Techval™ offers tailored validation programs to meet your specific operational and compliance needs.
Our Approach to Validation
At Techval™, our validation philosophy is grounded in risk-based, science-driven methodology. We focus on identifying critical quality attributes (CQAs) and critical process parameters (CPPs) to ensure your systems deliver repeatable, reliable, and compliant results.
Phased Approach:
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Assessment & Planning – Understanding systems, compliance requirements, and risk profiles.
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Protocol Development – Creating validation protocols (IQ, OQ, PQ) aligned with current GMP and regulatory guidelines.
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Execution & Testing – Conducting precise validation tests using calibrated instruments and documented procedures.
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Reporting & Documentation – Delivering structured, traceable, and audit-ready reports.
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Ongoing Support – Continuous monitoring and revalidation services to maintain compliance over time.