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Akrivis Pharma Pvt Ltd ISO 9001:2015 Certified
What we offer
Services
Pharmaceutical testing
Pharmaceutical products are tested to make sure they adhere to strict safety and quality requirements. This testing is being done to assist enhance public health in addition to saving the producer money and time.
Analytical Method Validation
Analytical validation provides experimental proof that a procedure, approach, or study regularly yields precise, repeatable, and accurate results by following established and recognized protocols.
Analytical Method Development
used to identify, separate, quantify, and learn more about the chemical components in drug products intended for commercial manufacturing
Dissolution Testing
We have a complementary variety of dissolve testing equipment accessible in the laboratory where Akrivis provides dissolution testing development services USP 1, USP 2, USP 3, USP 4 Apparatus are been Used.
Finished products
Analysis of the finished Drug products by using suitable methods.
Stability Studies
To determine, after assessing the stability data and testing a minimum of three batches of the medication substance
Related Substance
Controlling degrading impurities is the primary goal of a related substances test for dosage form monographs. Limiting contaminants that arise during the synthesis of the active pharmaceutical ingredient (API) is a further goal, nevertheless, and should be pursued whenever
Excipient and Impurities Testing
Excipient testing is a regulatory requirement that verifies the identity, purity, strength, and quality of raw materials. It's also necessary to confirm the safety and efficacy of a final drug product and Impurity testing is the process of identifying and isolating unknown materials in chemicals, polymers, packaging, pharmaceuticals, and finished products
Why Us
Best services available
AKRIVIS PHARMA PVT LTD is an independent pharmaceutical
Analytical Research and Development organization located in Hyderabad with the motto of providing precise results by using VariousAnalytical Techniques.
- Efficient Delivery
- Quality Assurance
- Regulatory Compliance
- Research Excellence
- Patient Support
- Reliable Supply
Akrivis Pharma Pvt Ltd
Akrivis Pharma Pvt Ltd is a ISO 9001:2015 Certified company
Akrivis Pharma Pvt Ltd
Akrivis Pharma Pvt Ltd is a ISO9 9001:2015 Certified company
Instrumentation
- High-performance liquid chromatography
- Dissolution Test Apparatus
- Ultra-performance liquid chromatography
- UV-VIS Spectrophotometer
- Disintegration apparatus
- Infrared spectroscopy
- Differential Scanning Calorimetry
- SEM
- Particle size analyser
Analytical method development and Analytical method validation
The parameters evaluated for the method development and validation include:
- Precision (method, intermediate and system)
- Accuracy (recoveries)
- Linearity
- Limit of detection (LOD)
- Limit of quantification (LOQ)
- Robustness
- Forced degradation
- System Suitability
- Specificity including forced degradation
- Stability of solution
- Filter compatibility
- Range
The procedure followed for Analytical Method Validation :
- Designing Method Validation Protocol
- Getting approval
- Initiating the analysis
- Sharing Validation Report