Comprehensive Water Purification System Validation services to verify the performance, reliability, and regulatory compliance of purified water, water for injection (WFI), and other pharmaceutical water systems.
Our validation experts perform qualification, testing, and documentation to ensure your water purification systems consistently meet industry standards, GMP requirements, and product quality expectations.
Our pharmaceutical testing services are backed by recognized accreditations.
Accredited as per ISO/IEC 17025:2017, demonstrating technical competence, quality management systems, and reliability in testing and calibration services.
Approved laboratory for testing pharmaceutical materials, microbiological samples, water systems, and food products in compliance with applicable regulatory standards.
We provide validation services for pharmaceutical water systems to ensure compliance with global standards.
Ensuring system performance, consistency, and compliance with pharmacopeial requirements.
Pharmaceutical manufacturing units install water production, storage and distribution systems to produce highly pure water which is used directly or indirectly in manufacturing.
The quality of this water requires to be compliant with regulatory requirements to be suitable for use as it has a significant impact on quality of finished products, intermediate reagents as well as washing of pharmaceutical equipment.
Hence, Water purification systems are to be validated as per regulatory requirements to demonstrate that they meet required design and operational qualifications and are capable to produce purified water with consistency and reproducibility.
RO systems, purified water systems, DI water systems, WFI systems, and distribution loops.
Yes, Validation is mandatory requirement of WHO, GMP and all pharmacopeia.
Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ) and Periodic Re-validation. There are three phases of Qualification. Phase I is the Investigation phase which requires minimum 14 days of continuous operation. Phase II is the Verification phase which requires a test period of 2-4 weeks and Phase III is typically run for one year after satisfactory completion of phase II. After all phases are completed, water system performance is verified through routine plan.
Ensure your water purification systems consistently meet regulatory standards and product quality requirements with our expert validation services.
* We Also Offer Sample Collection Services From Your Company or Location Across All Over Gujarat.
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