Empowering Compliance.
Elevating Quality.
Your trusted partner in pharma validation, digital transformation, and audit compliance.
Techval™ Services
Techval™ Services is an independent service provider offering comprehensive validation and qualification solutions tailored for the pharmaceutical (injectable, OSD, API), biotechnology, medical device, and healthcare sectors.
Specialists in Regulatory-Driven Validation and Compliance Solutions.
Comprehensive validation and qualification solutions tailored for pharmaceutical, biotechnology, medical device, and healthcare sectors.
Our Mission
We align every service with global regulatory expectations including FDA, EU-GMP, WHO, and MHRA. With a team of experienced professionals and a commitment to technical precision, Techval ensures your systems, environments, and documentation are fully compliant, audit-ready, and built for operational excellence.
Why Choose Techval™
Choose Techval™ as your trusted partner in validation—ensuring the integrity, performance, and compliance of your critical systems and environments. We deliver end-to-end solutions with meticulous attention to regulatory requirements.
Our Services
We Expertise In
Computer System Validation (CSV)
HVAC Validation & Thermal Mapping
CQV (Commissioning, Qualification And Validation)
Process & Cleaning Validation
Compressed Air & Nitrogen Gas Testing
Temperature Mapping & Environmental Monitoring
Computer System Validation (CSV)
Techval provides end-to-end Computer System Validation services in line with global regulatory standards such as FDA 21 CFR Part 11, ISPE GAMP 5, and EU Annex 11. We specialize in validating manufacturing control systems (PLCs, HMIs, SCADA), lab/QC instruments (HPLC, GC, UV, FTIR, Dissolution, etc.), and custom software platforms using a structured V-model approach. Our expert team ensures data integrity, audit trail functionality, electronic signature compliance, and system reliability across GxP environments. From URS and FS to Risk Assessments, IQ, OQ, and PQ, we provide tailored, inspection-ready documentation that meets global regulatory expectations. Empower your compliance strategy with Techval-where technology meets trust.
Manufacturing Systems
We specialize in validating manufacturing control systems (PLCs, HMIs, SCADA) using a structured V-model approach.
Laboratory Instruments
Validation of lab/QC instruments including HPLC, GC, UV, FTIR, Dissolution, and other analytical equipment.
Data Integrity
Our expert team ensures data integrity, audit trail functionality, electronic signature compliance, and system reliability across GxP environments.
Documentation
From URS and FS to Risk Assessments, IQ, OQ, and PQ, we provide tailored, inspection-ready documentation that meets global regulatory expectations.
HVAC Validation/Clean room Validation
We specialize in HVAC system qualification for pharmaceutical and biotech cleanrooms, ensuring regulated environmental conditions are met consistently. Our services include air velocity, HEPA filter integrity testing, recovery time testing, ACPH, temperature & RH,differential pressure monitoring, NVPC and airflow visualization studies. With adherence to ISO 14644 standards and EU-GMP Annex1
guidelines. Our validation strategy applies a risk-based approach, tailored to your facility’s unique design and operational parameters. We validate HVAC & LAF/RLAF/ DPB/PGC/SGC etc. systems under dynamic (in-operation) and at-rest (static) conditions to ensure ongoing compliance and optimal environmental control.
Testing Services
✓ Air velocity testing
✓ HEPA filter integrity testing
✓ Recovery time testing
✓ ACPH, temperature & RH
✓ Differential pressure monitoring
✓ NVPC and airflow visualization studies
Standards & Approach
With adherence to ISO 14644 standards and EU-GMP Annex1 guidelines, our validation strategy applies a risk-based approach, tailored to your facility’s unique design and operational parameters.
We validate HVAC & LAF/RLAF/DPB/PGC/SGC etc. systems under dynamic (in-operation) and at-rest (static) conditions to ensure ongoing compliance and optimal environmental control.
Temperature Mapping & Environmental Monitoring
Ensuring Temperature & Humidity Compliance Across Critical Areas ›› Techval Services delivers comprehensive Thermal Mapping Studies for temperature and relative humidity (RH) monitoring of pharmaceutical production areas, warehouses, QC instruments, stability chambers, cold rooms, freezers, incubators, and warehouses, QC instruments, stability chambers, cold rooms, freezers, incubators, and transport vehicles. Utilizing calibrated data loggers and industry-standard protocols,
we rigorously assess environmental conditions to ensure uniform temperature distribution and identify potential hot and cold spots. ›› Our in-depth analysis safeguards product quality by verifying storage and transport conditions meet stringent regulatory requirements. Each thermal mapping study is
supported by a detailed validation protocol and a comprehensive final report designed
supported by a detailed validation protocol and a comprehensive final report designed to facilitate regulatory inspections and internal audits. Our services ensure your critical environments comply with WHO, FDA, EU GMP
Annex 1, and MHRA guidelines, providing confidence in product integrity throughout
the supply chain.
Comprehensive Studies
Techval Services delivers comprehensive Thermal Mapping Studies for temperature and relative humidity (RH) monitoring of pharmaceutical production areas, warehouses, QC instruments, stability chambers, cold rooms, freezers, incubators, and transport vehicles.
Technology & Analysis
Utilizing calibrated data loggers and industry-standard protocols, we rigorously assess environmental conditions to ensure uniform temperature distribution and identify potential hot and cold spots.
Quality Assurance
Our in-depth analysis safeguards product quality by verifying storage and transport conditions meet stringent regulatory requirements. Each thermal mapping study is supported by a detailed validation protocol and a comprehensive final report.
Regulatory Compliance
Our services ensure your critical environments comply with WHO, FDA, EU GMP Annex 1, and MHRA guidelines, providing confidence in product integrity throughout the supply chain.
Additional Services
Airflow Visualization (Smoke Study)
Ensuring Critical Environment Integrity in Sterile Injectable Facilities.
Our GMP-compliant Airflow Visualization Studies videos provide visual confirmation of
airflow patterns within critical areas to verify unidirectional airflow and detect
turbulence or dead zones in critical environments. Using non-toxic smoke, we assess
turbulence or dead zones in critical environments. Using non-toxic smoke, we assess
airflow behavior in Grade A/B cleanrooms, laminar flow units, isolators, BSCs, filling
lines, and sterile compounding zones. Our studies support area qualification, HVAC
validation, and deviation investigations, providing high-resolution video and reports
aligned with EU GMP Annex 1, ISO 14644-3, and WHO TRS 961—ensuring
contamination control and regulatory compliance
IT Infrastructure Services
Techval designs and validates robust IT infrastructure tailored to
regulated industries. We offer secure installation of servers, network systems, data
backup solutions, and software environments for manufacturing and compliance
purposes. Our approach ensures data integrity, business continuity, and GXP
alignment. From system hardening to IT SOPS, we provide end-to-end solutions that
align with regulatory and cybersecurity expectations.
Calibration Services
Techval offers calibration services for instruments and equipment used
in pharmaceutical, biotech, and cleanroom environments. We ensure
traceability to national/international standards and deliver certifi-
cate-backed reports for regulatory compliance. Whether it’s thermocou-
ples, pressure gauges, or particle counters, our calibration services en-
hance measurement accuracy and quality assurance.
Pharmaceutical Equipment Solutions
Standard Equipment In SS, MS, And Aluminium For Production, Labs, And Packaging, With Full Qualification Support.
Digital Marketing
Our creative team provides strategic digital marketing services to help
healthcare and industrial brands stand out. We design user-friendly
websites, execute SEO strategies, manage social media campaigns,
and create branding materials aligned with your identity. Whether you’re
launching a new product or expanding online reach, our services ensure
a professional, compliant, and engaging digital presence.
Audit Readiness & Documentation
Every audit is an opportunity to prove your compliance strength. Techval
Consultancy services for writing documents i.e., SOP, Protocol, Report, cleaning
validation, Media fill, Process Validation, Aseptic process validation (Media fill) etc.
Vendor/third party audit & 21 CFR210/211 Compliance.
Whether it’s FDA, WHO, MHRA, or client audits, we help you walk in with confidence.