The Foundation of Excellence – Quality & Compliance at Pharmatech Process Equipments

At Pharmatech Process Equipments Process Equipments, quality isn’t just a standard – it’s the foundation of everything we do. From designing and developing advanced process equipment to delivering turnkey solutions, our commitment to uncompromising quality and regulatory compliance ensures that our customers in the Pharmaceutical, Biotechnology, API & Fine Chemicals and Cosmetic industries receive the most reliable, efficient, and compliant equipment.

Adhering to Global Quality Standards

We manufacture process systems that align with international regulations, including:

cGMP (Current Good Manufacturing Practices)
USFDA (U.S. Food and Drug Administration) standards
EU-GMP guidelines
PED (Pressure Equipment Directive) & CE mark Compliant
U stamp certified equipment with UL approved electrical & automation system
ASME-BPE for biopharmaceutical applications
EHEDG (European Hygiene Engineering & Design Group) Guidelines

Every piece of equipment, from sterile process vessels to automation-integrated systems, is engineered with precision, durability, and compliance at its core.

Innovation Meets Compliance

Our automation-driven solutions, including PLC-based control systems with SCADA, ensure that customers can monitor and control their processes with the highest level of accuracy. We integrate real-time data acquisition to support process compliance with 21CFR SCADA Part 11 regulations, enabling secure and traceable manufacturing.

Comprehensive Qualification & Validation Support

cGMP-Compliant Cultivation: Ensures your production meets the highest regulatory and quality standards.
Advanced Mixing Performance: Features diverse agitators tailored for superior mixing across various products and processes.
Integrated Cleaning/Sterilization (CIP/SIP): Minimizes downtime while ensuring thorough cleaning and sterilization.
Scalable Production: Ranges from 10L to 50,000L capacities to meet your growing needs, all adhering to cGMP, ASME, PED, and CE standards.
Automated/Semi-Automated Systems: Incorporates state-of-the-art SCADA and PLC systems for enhanced efficiency and data integrity, fully compliant with 21 CFR Part-11.

Commitment Beyond Compliance

Commitment Beyond Compliance

At Pharmatech Process Equipments, compliance isn’t just about following regulations – it’s about ensuring safety, efficiency, and long-term reliability. Our team is dedicated to continuous improvement, process automation, and customer-centric innovation, making us a trusted partner for pharmaceutical manufacturers worldwide.

By leveraging advanced engineering, embracing automation, and adhering to the highest quality standards, we help our customers build robust, future-ready manufacturing systems.

Let’s build the future of high-quality, compliant, and efficient process solutions together.

Contact us today to learn how Pharmatech Process Equipments can support your manufacturing goals with precision-engineered, globally compliant solutions.

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