All Posts - Pharma Egg

Jan132022 by KBS.No Comments

Pharmaceuticals Quality Control Lab Servies

For Maintain the Quality and Development of Drugs, Pharmaceuticals Quality Control Lab Services are performed. Here are some of them given below. Analytical Testing Services Method Development / Validation Bioanalytical Testing Assay Development Clinical Trials Services Raw Material Testing Services Packaging Testing Contract Pharma Services CRO Services / Outsourcing

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...

Jan112022 by KBS.No Comments

Olanzapine 5mg Tablet Standard Analytical Procedure

Testing Methods, Product

Olanzapine 5mg tablet belongs to a category of medication known as ordinary antipsychotics. It works with the aid of using assisting to repair the stability of positive herbal materials withinside the brain. Talk to the medical doctor approximately the dangers and blessings of treatment (particularly whilst utilized by teenagers). See additionally Precautions section. Olanzapine 5mg Tablet Standard Analytical Procedure deals with the testing method of olanzapine tablet-like general test physical test dissolution disintegration etc. Now we move to our SAP Olanzapine 5mg Tablet Standard Analytical Procedure REFRENCE: UNITED STATES PHARMACOPOEIA APPROVAL BLOCK Written By: Quality Control Analyst Signature/Date Reviewed By: Quality Control Manager Signature/Date...

Jan82022 by KBS.No Comments

Amlodipine Besylate Raw Material (API) SAP

Raw Material, Testing Methods

Amlodipine Besylate Raw Material (API) is the best-prescribed Raw Material (API) for cardiovascular ailment main hazard element for high blood pressure. First mentioned low fee ultraviolet-seen method for the dedication and quantitation of medicine in prescription drugs and organic fluids. Chromatographic strategies have an utility with appreciate to hint evaluation. Different sorts of chromatography together with excessive-overall performance liquid chromatography, excessive overall performance skinny layer chromatography have maximum common packages withinside the subject of pharmaceutical in addition to biomedical analyses. Amlodipine Besylate Raw Material (API) Chromatography mixed with mass spectrophotometry has the capacity to acquire molecular ion. Amlodipine Besylate Raw Mater...

Jan42022 by KBS.No Comments

Calibration SOPs for UV Spectrophotometer

SOPs

Calibration is one of the most frequently used techniques in pharmaceutical analysis. This involves measuring the amount of ultraviolet radiation or seen absorbed by a substance in the solution. The calibration instrument measures the ratio, or function ratio, from the intensity of two light beams in Qualitative UV analysis, organic compounds can be identified using spectrophotometers, if there are recorded data available, and quantitative spectrophotometric analysis is used to ensure the quantity of molecular species that absorb radiation. Calibration of spectrophotometric techniques are simple, fast, quite specific and applies to small quantities of compounds. Fundamental law that regulates calibration spectrophotometrically analysis PURPOSE: To describe the Calibration procedure for...

Jan42022 by KBS.No Comments

Operational SOPs for UV/VIS Spectrophotometer

SOPs

UV/VIS Spectrophotometer Operational SOPs method is used to measure the pharmaceutical and non-pharmaceutical compounds that have detectable peaks in the UV-Vis region PURPOSE: To describes the operating procedure for operation of UV/VIS Spectrophotometer. SCOPE: This SOP gives detailed outline for the operation of UV/VIS Spectrophotometer and will cover operating procedure of equipment. RESPONSIBILITY: QC Analyst is responsible for operation of equipment and preparing standard operating procedure. It is the responsibility of QC Manager to assist and ensure Operating Procedure’s as per SOP and to make certain that this SOP is followed in its entirety, reviewed regularly and revised as necessary. REFERENCE: In-House Specifications MATE...

Jan42022 by KBS.No Comments

HPLC Waters Pda With Quartnary Pump – SOPs

SOPs

This SOP HPLC WATERS PDA WITH QUARTNARY PUMP most important who gives a detailed outline for the operation of HPLC 1 Waters PDA With Quartnary Pump and will cover the operating procedure, calibration and cleaning of equipment. PURPOSE: To describes the operating procedure for operation of HPLC 1 Waters PDA With Quartnary Pump. SCOPE: This SOP gives detailed outline for the operation of HPLC 1 Waters PDA With Quartnary Pump and will cover operating procedure, calibration and cleaning of equipment. RESPONSIBILITY: QC Analyst is responsible for the operation of equipment and preparing standard operating procedures. It is the responsibility of QC Manager to assist and ensure Operating Procedure as per SOP and to make certain that this SOP is ...

Jan32022 by KBS.1 Comment

Cleaning SOPs for UV Spectrophotometer

SOPs, Quality Control

In this article detail is given of Cleaning SOPs for UV Spectrophotometer, how to clean UV Spectrophotometer in Quality control Laboratory of Pharmaceuticals. OBJECTIVE To lay down the procedure for cleaning of UV/VIS Spectrophotometer. SCOPE: This shall be applicable to the UV/VIS Spectrophotometer installed in Quality Control instrument Laboratory. RESPONSIBILITY: Technical Assistant/ Helper. C Analyst. ACCOUNTABILITY: Manager-Quality Control. MATERIAL AND EQUIPMENT: UV/VIS Spectrophotometer. Clean dry cloth. Tissue paper. Dilute soap solution. Purified water. PROCEDURE: Ensure that the power supply to the instrument is switched OFF before cleaning. After completion of the testing, remove cuve...

Jan32022 by KBS.No Comments

Washing Of HPLC Column SOP

SOPs

Here is the WASHING OF HPLC COLUMN, it is very important in the laboratory, if not done can correctly affect the health of your column. Cleaning your HPLC column may be simple, but it is very important for efficiency, lifetime, and productivity instruments. The ineffective HPLC column can affect your analysis, resulting in inaccurate results, which means more time spent on the same project. The following SOP focuses only on how to clean your HPLC column through reverse flushing. It may be time to water your HPLC column when you see high back pressure, low efficiency, split peak, or the most common problem, the particulate buildup in the head of the column. Now we move to Washing Of HPLC Column SOP Objective: This method is applicable for washing of HPLC column. Sco...