Accurate testing and analysis of pharmaceutical materials and dosage forms to ensure quality, safety, and compliance with global pharmacopeial standards.
Pharmaceutical testing plays a critical role in ensuring product quality, safety, and compliance with regulatory standards. At Siddhi Green, we provide comprehensive testing services for pharmaceutical materials and dosage forms using advanced analytical techniques and standardized methodologies.
Our services are aligned with major pharmacopeial standards including IP, USP, EP, BP, JP, and CP, ensuring reliable and globally accepted results.
ICP-OES can detect a wide range of
elements found in the periodic table with
detection limits upto ppb levels
Our laboratory is equipped with advanced analytical instruments to ensure precise and reliable testing.
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.
Pharmaceutical materials include Active Pharmaceutical Ingredients (API), raw materials, finished goods as well as pharmaceutical (drug) intermediates.
We analyze pharmaceutical materials in accordance with IP, USP, EP, BP, JP, CP as well as BIS.
Non-complex physico-chemical tests involving techniques such as gravimetric, titrimetric, limit tests, UV, FTIR and visual observations are completed within 1–2 working days. Complex techniques such as Gas Chromatography, HPLC, ICP-OES, AAS usually take 2–5 working days depending on the test protocol.
It depends on reference standard requirement of the test. For pharmacopeial standards, we require reference standard to be provided by the customer.
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.
We combine technical expertise, advanced instrumentation, and regulatory knowledge to deliver reliable testing solutions
Ensure quality, safety, and compliance of your pharmaceutical products with our expert testing services.
* We Also Offer Sample Collection Services From Your Company or Location Across All Over Gujarat.
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