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Testing Methods

The testing methods category contains all types of testing-related information such as Products testing, Raw Material testing, Pharmaceuticals ingredients (Active, Excipient) and Packaging material, etc. More data is appended below

 

Sampling and Testing of Packing Materials

Sampling and Testing of Packing Materials

Testing Methods, Production, Quality Assurance, Quality Control
The Sampling and Testing of Packing Materials should take account of at least the following: the quantity received, the quality required, the nature of the material (e.g. primary packaging materials and/or printed packaging materials), the production methods, and what is known of the Quality Assurance system of the Sampling and Testing of Packing Materials manufacturer based on audits. The number of samples taken should be determined statistically and specified in a sampling plan. Sampling and Testing of Packing Materials is an important operation in which only a small fraction of a batch is taken. Valid conclusions on the whole cannot be based on tests which have been carried out on non representative samples. Correct sampling is thus an essential part of a system of Quality Assurance....
Sampling and Testing of In process and Finished Products

Sampling and Testing of In process and Finished Products

Quality Control, Product, Production, SOPs, Testing Methods
The objective of in Sampling and Testing of In process and Finished Products is to verify that all applicable specifications and requirements pertaining to product are fulfilled and to prepare corresponding documents so as to check that testing parameters met the intended specifications and requirements through out the production run. Purpose:- This SOP is established to provide the guidelines for the sampling & testing of in process and finished products so as to get the representative sample of the whole batch for analysis. Sampling and Testing of In process and Finished Products Additionally, the objective of the in process & final testing is to provide objective evidence of product conformance to specification and continued effectiveness of the quality management system. ...
Product Processes and Quality of In Process Material

Product Processes and Quality of In Process Material

Quality Control, General Topics, SOPs, Testing Methods
The purpose of a Product Processes and Quality of In Process Material system is to provide staff and management with objective insight into the process and related work products. Your process and product quality approach supports the delivery of high-quality products by providing project staff and managers at all levels with appropriate visibility into the process and related work products throughout the life of the pharmaceuticals. Product Processes and Quality of In Process Material Objective:- To ensure compliance of Product Processes and quality of in process material. Responsibility:- Section Supervisor Production Manager QA Incharge Procedure:- Issuance of Raw Material & Packaging Components Check the product name, strength, printing quality and quantity o...
Zinc Oxide Testing by Alternate Method

Zinc Oxide Testing by Alternate Method

Testing Methods
USP is updating the General Chapter Zinc Oxide Testing by Alternate Method  Determination of the monograph to include ion chromatography as a method for the assay. Zinc oxide is used in various skin care creams, drugs, and drug products. The ion chromatography analysis involves the separation of zinc followed by a post-column reaction using 4-(2-pyridylazo) resorcinol (PAR) reagent and subsequent detection at 530 nm wavelength. Sample preparation consisted of 0.1868 g of sample dissolved in 10 mL 6 mol/L HCl and made up to 100 mL with ultrapure water. PURPOSE This Raw material Specification & Analysis prescribes the requirements for Zinc Oxide Testing by Alternate Method, which is one of the components of a Capsule, tablet, and AX tablet. SCOPE It is applicable in the Material, Pr...
Meloxicam 7.5mg Injection Testing by UV Method and In House Method

Meloxicam 7.5mg Injection Testing by UV Method and In House Method

Testing Methods
Meloxicam testing by UV method and In House method 2, meloxicam is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by the breakdown of the joint lining) and rheumatoid arthritis (arthritis caused by inflammation of the joint lining) Meloxicam 7.5mg Injection Testing by UV Method and In House Method is also used to relieve pain, tenderness, swelling, and stiffness caused by juvenile rheumatoid arthritis (a type of arthritis that affects children) in children 2 years of age and older. . Meloxicam is in a class of drugs called non-steroidal anti-inflammatory drugs (NSAIDs). It works by blocking the body's production of substances that cause pain, fever, and inflammation. PURPOSE To describe the operational procedure Meloxicam 7.5mg In...
Montelukast Sodium Testing Procedure

Montelukast Sodium Testing Procedure

Testing Methods, Raw Material, SOPs
Montelukast Sodium Testing Procedure and Raw Material specification & analysis prescribes the requirements with UV Spectrophotometer spectrum and Alternate Method of Analysis on HPLC System and Other Testing procedures. Characters Spread about 1.0 of sample on a clean, dry watch glass and observe the appearance, it should be white crystalline powder and determination. Solubility (i) Take approximately 0.5 gram of sample into a clean test tube containing water. Close the test tube with stopper and shake well. The sample slightly soluble in water. (ii) Take approximately 0.5 gram of sample into a clean test tube containing alcohol. Close the test tube with stopper and shake well. The sample slightly soluble in alcohol. (iii) Take approximately 0.5 gram of sample into a clean tes...
How To Test Naproxen Sodium Raw Material

How To Test Naproxen Sodium Raw Material

Testing Methods, Raw Material, SOPs
How To Test Naproxen Sodium Raw Material specification & analysis prescribes the requirements with UV Spectrophotometer spectrum and Alternate Method of Analysis on HPLC System and Other Testing procedures. Characters How To Test Naproxen Sodium Raw Material Spread about 1.0 of sample on a clean, dry watch glass and observe the appearance, it should be white to creamy crystalline powder Solubility Soluble in water and in methanol; sparingly soluble in alcohol; very slightly soluble in acetone; and practically insoluble in chloroform and in toluene. Melting point Melts at about 225 °C with determination decomposition Procedure: Grind the Naproxen Sodium sample into a fine powder in a mortar and pack the capillary tube with sample by tapping on a hard surface so as to form a...
Paracetamol Raw Material Testing By UV Method

Paracetamol Raw Material Testing By UV Method

Testing Methods, Raw Material, SOPs
Paracetamol Raw Material Testing By UV Method specification & analysis prescribes the requirements with UV Spectrophotometer spectrum and Alternate Method of Analysis on HPLC System and Other Testing procedures. Paracetamol Raw Material Testing By UV and Purpose This raw material specification & analysis prescribes the requirements for Paracetamol raw material Testing UV and HPLC Method. Characters Spread about 1.0 of sample on a clean, dry watch glass and observe the appearance, determination it should be white, crystalline powder. Solubility Sparingly soluble in water, freely soluble in alcohol, very slightly soluble in methylene chloride. Identification Melting point:- 168 °C to 172 °C Procedure: Paracetamol Raw Material Testing By UV Method, Grind the Paracetamol s...
Ranitidine HCl Testing UV and HPLC Method

Ranitidine HCl Testing UV and HPLC Method

Testing Methods, Raw Material, SOPs
Ranitidine HCl Testing UV and HPLC Method Raw Material specification & analysis prescribes the requirements with UV Spectrophotometer spectrum and Alternate Method of Analysis on HPLC System and Other Testing procedures. Ranitidine HCl Testing UV and HPLC Method and Purpose This raw material specification & analysis prescribes the requirements for Ranitidine HCl raw material Testing UV and HPLC Method. Characters Ranitidine HCl Testing UV and HPLC Method is spread about 1.0 of sample on a clean, dry watch glass and observe the appearance, it should be white to pale yellow, crystalline, practically odorless powder. Is sensitive to light and moisture. Melts at about 140º, with decomposition. Solubility Ranitidine HCl Very soluble in water; sparingly soluble in alcohol. Melt...
Dextromethorphan Hydrobromide Raw Material Testing

Dextromethorphan Hydrobromide Raw Material Testing

Testing Methods, Raw Material
Dextromethorphan Hydrobromide Raw Material Testing specification & analysis prescribes the requirements with IR spectrum and Alternate Method of Analysis on UV System and Other Testing procedures. Dextromethorphan Hydrobromide Raw Material Testing PURPOSE This raw material specification & analysis prescribes the requirements Dextromethorphan Hydrobromide Raw Material Testing which is used in Syrup & Tablet. 1.0 PURPOSE This raw material specification & analysis prescribes the requirements for Dextromethorphan Hydrobromide which is one of the components of Syrup & Tablet. 2.0 SCOPE It is applicable in Material Department, Product Development and Quality Assurance Department to confirm its physical and chemical specifications. 3.0 REFERENCES USP/BP 4.0 DE...