pharmablog.in

Mr. Shaikh is the professional pharmaceuticals blogger, founder and author of pharmablog.

ICH Guidelines

The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) is an organization that develops guidelines and standards to ensure the global harmonization of the development, registration, and post-approval phases of pharmaceutical products. ICH brings together regulatory authorities and the pharmaceutical industry to create consensus on various aspects of drug development.

ICH Guidelines Read More »

SCHEDULE L-1 (GLP)

Schedule L1 Drugs and Cosmetics Act | Schedule L in Pharma | Schedule L1 Guidelines | GOOD LABORATORY PRACTICES AND REQUIREMENTS OF PREMISES AND EQUIPMENTS General Requirements: Premises: Personnel: Equipments: Chemicals and Reagents: Good house keeping and safety: Maintenance, calibration, and validation of equipments: Reference materials: Microbiological Cultures: Quality system: Internal quality system audits: Management

SCHEDULE L-1 (GLP) Read More »

Calibration of Gas Chromatography SOP

SOP for Calibration of Gas Chromatography in Pharmaceutical Industry | SOP of Gas Chromatography | GC Calibration | 1.0 OBJECTIVE : 2.0 SCOPE : 3.0 RESPONSIBILITY : 4.0 ACCOUNTABILITY: 5.0 PROCEDURE : 5.1 SAFETY AND PRECAUTIONS: 5.2 PRELIMINARY CHECK BEFORE STARTING THE INSTRUMENT: 5.3 GENERAL SETUP: 5.4 CALIBRATION: 5.4.1 GAS FLOW RATE CALIBRATION: Parameter Set

Calibration of Gas Chromatography SOP Read More »

Analyst Qualification Criteria

Pharmaceutical Industry Analyst Qualification Criteria | Analyst Qualification for Quality Control Laboratory | Group Sr. No. Analytical Technique Qualification Procedure Acceptance Criteria A   PHYSICAL PARAMETERS (Non-complex Analytical Techniques)  1 Description / Characteristics To be performed on routine sample with Qualified Analyst (single analysis) Individual results must comply with the specifications  2 Solubility  3 Appearance

Analyst Qualification Criteria Read More »

Residue on ignition / Sulfated ash

Sulphated ash procedure as per BP / IP | Residue on ignition procedure as per USP | Sulfated ash test method | Sulfated ash formula | The Residue on Ignition/Sulfated Ash test uses a procedure to measure the amount of residual substance not volatilized from a sample when the sample is ignited in the presence of sulfuric acid

Residue on ignition / Sulfated ash Read More »

Loss on drying

Why loss on drying is performed in pharmaceuticals | Loss on drying procedure | Loss on drying (LOD) is a common test method used in various industries, including food, pharmaceuticals, and manufacturing, to determine the moisture content of a material. The loss on drying test is performed in pharmaceuticals to measure the amount of water and volatile

Loss on drying Read More »