Product - Pharma Egg

Mar152023 by KBS.No Comments

SOP for Metformin Hydrochloride and Sitagliptin Phosphate Tablet Testing by UV and HPLC Method

Sitagliptin + Metformin HCl Tablet is a combination medication used to treat type 2 diabetes. Testing for this medication typically involves a combination of preclinical and clinical studies to evaluate its safety, efficacy, and pharmacokinetics. Preclinical studies involve testing the medication in animal models to determine its toxicity, pharmacokinetics, and pharmacodynamics. These studies help researchers identify any potential safety concerns and determine appropriate dosages for humans' SOP for Metformin Hydrochloride and Sitagliptin Phosphate Tablet Testing by UV and HPLC Method. Clinical studies involve testing the medication in human subjects to evaluate its safety and efficacy. These studies are typically conducted in several phases, starting with small studies on unhealthy...

Mar32023 by KBS.No Comments

SOP for Diclofenac Sodium SR 100mg Tablet Tested UV and HPLC Methods

Testing Methods, General Topics, Product, SOPs

SOP for Diclofenac Sodium SR 100mg Tablet Tested UV and HPLC Methods to determine its purity and quality. Both UV and HPLC methods are widely used in pharmaceutical laboratories to test the quality and purity of diclofenac sodium tablets. These methods are highly accurate and reliable and are used to ensure that the tablets meet the required quality standards. PURPOSE: To describe the procedure for analysis at in-process and finished stage of Diclofenac Sodium SR 100mg Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of Diclofenac Sodium SR 100mg Tablet and will cover In process testing activities on a physical, chemical & instrumental basis. RESPONSIBILITY: QC Analyst is responsible for physical / chemical testing and preparing standard analytic...

Mar32023 by KBS.No Comments

SOP for Vonoprazan 10 mg Tablet Testing Procedure

Testing Methods, General Topics, Product, SOPs

Vonoprazan Fumarate is a medication used to treat gastroesophageal reflux disease (GERD) and other gastrointestinal disorders. The SOP for Vonoprazan 10 mg Tablet Testing Procedure should follow the appropriate regulatory guidelines and be validated to ensure the accuracy, precision, and reliability of the results. PURPOSE: To describe the procedure for analysis at in-process and finished stage of Vonoprazan 10 mg Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of Vonoprazan 10 mg Tablet and will cover In process testing activities on a physical, chemical & instrumental basis. RESPONSIBILITY: QC Analyst is responsible for physical / chemical testing and preparing standard analytical procedure. It is the responsibility of QC Manager to assist an...

Mar22023 by KBS.No Comments

Trimetazidine Hydrochloride MR 35mg Tablet Testing Procedure SOP

Testing Methods, General Topics, Product, SOPs

Trimetazidine Hydrochloride MR 35 mg Tablet assay testing is a process to determine the potency of the active ingredient in the medication. This Trimetazidine Hydrochloride MR 35mg Tablet Testing Procedure SOP ensures that the medication contains the correct amount of the active ingredient, trimetazidine hydrochloride, which is necessary for it to be effective. PURPOSE: To describe the procedure for analysis at in-process and finished stage of Trimetazidine Hydrochloride MR 35 mg Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of Trimetazidine Hydrochloride MR 35 mg Tablet and will cover In process testing activities on a physical, chemical & instrumental basis. RESPONSIBILITY: QC Analyst is responsible for physical / chemical testing and prepar...

Mar22023 by KBS.No Comments

SOP for Testing Itopride 50mg Tablet by UV spectroscopy

Testing Methods, General Topics, Product, SOPs

UV (Ultraviolet) testing is a commonly used technique in the pharmaceutical industry to determine the purity and concentration of a drug substance or a drug product. SOP for Testing Itopride 50mg Tablet by UV spectroscopy is based on the measurement of the absorption of UV light by a compound in a solution. PURPOSE: To describe the procedure for analysis at in-process and finished stage of Itopride 50 mg Tablet. SCOPE: This SAP gives a detailed outline for the finished product analysis of Itopride 50 mg Tablet and will cover In process testing activities on a physical, chemical & instrumental basis. RESPONSIBILITY: QC Analyst is responsible for physical / chemical testing and preparing standard analytical procedure. It is the responsibility of QC Manager to assist and ensure Tes...

Feb272023 by KBS.No Comments

SOP for Amlodipine 5mg/Valsartan 160mg/Hydrochlorothiazide 12.5mg Tablet Assay Testing

Testing Methods, General Topics, Product, SOPs

It is important to follow appropriate safety precautions when handling these drugs and to adhere to the manufacturer's instructions for the assay procedure of SOP for Amlodipine 5mg/Valsartan 160mg/Hydrochlorothiazide 12.5mg Tablet Assay Testing. PURPOSE: To describe the procedure for analysis at the in-process and finished stage of SOP for Amlodipine 5mg/Valsartan 160mg/Hydrochlorothiazide 12.5mg Tablet Assay Testing. SCOPE: This SAP gives a detailed outline for the finished product analysis of SOP for Amlodipine 5mg/Valsartan 160mg/Hydrochlorothiazide 12.5mg Tablet Assay Testing and will cover In process testing activities on physical, chemical & instrumental basis. RESPONSIBILITY: QC Analyst is responsible for physical / chemical testing and preparing standard analytical proce...

Feb272023 by KBS.No Comments

SOP for Tramadol 37.5 mg and Acetaminophen 325 mg tablet Assay Testing

Testing Methods, General Topics, Product, SOPs

Assay testing of a tramadol 37.5 mg and acetaminophen 325 mg tablet would typically involve the quantitative analysis of both active ingredients to determine their content or potency in the tablet. SOP for Tramadol 37.5 mg and Acetaminophen 325 mg tablet Assay Testing is important for ensuring the quality and consistency of the medication, as well as verifying that the tablet contains the expected amount of each active ingredient. Assay testing can be performed using a variety of analytical techniques, including high-performance liquid chromatography (HPLC), gas chromatography (GC), and spectrophotometry. The specific method used will depend on factors such as the properties of the active ingredients and the desired level of sensitivity. During the testing process, a sample of the ta...

Jan302023 by KBS.No Comments

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. ...

Jan122022 by KBS.No Comments

Diclofenac Sodium SR 100mg Tablet Standard Analytical Procedure

Testing Methods, Product

Diclofenac Sodium SR 100mg Tablet Standard Analytical Procedure Reference: United States Pharmacopoeia APPROVAL BLOCK Title Designation Signature/Date Written By: Quality Control Analyst Reviewed By: Quality Control Manager Verified By: Quality Assurance Incharge Approved By: Technical Operation Director Distribution List Sr. # Department New revision # Retrieval Revision # Signature & Date DOCUMENT REVISION CONTROL Rev. # Date Initiated By Page # Nature of Amendment Done By 1.0 PURPOSE 2.0 SCOPE 3.0 RESPONSIBILITY 4.0 REFERENCE 5.0 MATERIAL AND EQIUPMENT 6.0 PROCEDURE 7.0 RISK ANALYSIS 1.0 PURPOSE: To describes t...

Jan112022 by KBS.No Comments

Olanzapine 10mg Tablet Standard Analytical Procedure

Testing Methods, Product

If you're looking for Standard Analytical Procedure (SAP) of Olanzapine in order to use it for Pharmaceuticals then you're landed on the right page. In this blog post, we are going to share Olanzapine 10mg Tablet Standard Analytical Procedure also called SAP in short form. You can copy and paste this Olanzapine 10mg SAP in word and make it your own file. In order to remove format you can use notepad. Now we lets move to our SAP step by step. Olanzapine 10mg Tablet Standard Analytical Procedure Reference: United States Pharmacopoeia APPROVAL BLOCK Title Designation Signature/Date Written By: Quality Control Analyst Reviewed By: Quality Control Manager Verified By: Quality Assurance Incharge Approved By: Technical Operation Director D...