Skip to content
  • About Us
  • Contact Us
  • Research
  • Copyright Policy and Terms of Use
  • Disclaimer
  • Privacy
Pharma Beginners
  • About Us
  • Contact Us
  • Research
  • Copyright Policy and Terms of Use
  • Disclaimer
  • Privacy
Search this website
Menu Close
  • About Us
  • Contact Us
  • Research
  • Copyright Policy and Terms of Use
  • Disclaimer
  • Privacy
  • About Us
  • Contact Us
  • Research
  • Copyright Policy and Terms of Use
  • Disclaimer
  • Privacy

Equipment Usage Logbook – Procedure & Format

cGMP, GLP, QA Sop, QC Sop, Quality Control, SOPs entry is missed, Erroneous entries, Log book Maintenance, Logbook Issuance Procedure, wrong entry1 Comment on Equipment Usage Logbook – Procedure & Format

 Standard Operating Procedure (SOP) and Format for Instrument, Equipment usage logbook used for day to day activity and recording of usage details in pharmaceuticals. Equipment Usage Logbook 1.0   PURPOSE: This purpose of this SOP is to define the procedure for issuance, handling, making entries and review of   “Instrument/ Equipment usage logbook”. 2.0   SCOPE: This procedure […]

Calibration of Glassware (Laboratory)- Procedure

Calibration, cGMP, GLP, Protocol, QA Sop, QC Sop, Quality Control, SOPs Burette Calibration, Pipette Calibration, Volumetric Flask CalibrationLeave a Comment on Calibration of Glassware (Laboratory)- Procedure

Standard Operating Procedure (SOP) and Protocol for Calibration of Laboratory Glassware (Class A)  like- Volumetric flask, Pipette calibration, Burette calibration used in Quality Control Laboratory for analysis purpose. Glassware Calibration Procedure 1.0   Purpose: The purpose of this SOP is to describe the procedure for calibration of laboratory glassware. 2.0   Scope: This SOP is applicable for […]

Reference Solution – Preparation & Hold Time Study

cGMP, GLP, Protocol, QA Sop, QC Sop, Quality Control, SOPs Solution Hold Time, Solution Stability StudyLeave a Comment on Reference Solution – Preparation & Hold Time Study

Standard Operating Procedure (SOP) for Preparation, Handling and Hold Time Study of Reference Solution. In analytical chemistry, a standard solution is a solution containing a precisely known concentration of an element or a substance. A known weight of solute is dissolved to make a specific volume. It is prepared using a standard substance, such as […]

Analytical Method Transfer (USP 1224) Guideline

Audit, cGMP, Checklist, Checklist / Formats, GC, GLP, HPLC, Protocol, QA Sop, QC Sop, Quality Control, SOPs, Validation Analytical Method Validation (AMV) - Flow Chart, Co-validation, Collaborative Type of Method Transfer, Direct Method Transfer, Indirect Method Transfer, Method Transfer approach, Non-Collaborative Method Transfer, Three-Way Approach, Two-Way Approach1 Comment on Analytical Method Transfer (USP 1224) Guideline

Analytical Method Transfer (also called ‘Method Transfer’): A documented process that qualifies a laboratory (i.e., the Receiving Unit) to use an analytical test procedure that originated in another laboratory (i.e., the Transferring Unit), thus ensuring that the Receiving Unit has the procedural knowledge and ability to perform the transferred analytical procedure as intended Analytical Method […]

Microscope – Operation & Calibration Procedure

Calibration, cGMP, Micro Sop, Microbiology, SOPs, Sterile Microscope Calibration, Microscopy1 Comment on Microscope – Operation & Calibration Procedure

Standard Operating Procedure (SOP) for operation & calibration of digital microscope. A microscope consists of a compound magnifying system in which the observer looks at the first (primary) image with a lens that produces an enlarged secondary (virtual) image. Microscope – Operation & Calibration 1.0   Purpose: To lay down the procedure for operation and calibration […]

Environmental Monitoring Guide – Non Sterile Facility

Calibration, cGMP, Micro Sop, Microbiology, QA Sop, SOPs, Sterile, Validation EM Media PreparationLeave a Comment on Environmental Monitoring Guide – Non Sterile Facility

Guideline (SOP) for risk based Environmental Monitoring (EM) in Non Sterile drug manufacturing facility. Regulatory standards for non-sterile product manufacture and environmental control have not been consistently established, however, EU GMP requires inhalants to be manufactured in an ISO 8 environment and compendia, such as USP <1111> Microbiological Examination of Nonsterile Products. Procedure for Environmental […]

Environmental Monitoring (EM) – New Approach Guide

cGMP, Micro Sop, Microbiology, QA Sop, QC Sop, SOPs, Sterile, Validation Contamination Recovery Rates, Cut-off Value Approach, EM Media Preparation for Sterile, Neutralizing agents, Non-Parametric Tolerance, Non-Viable Particulates, Normal Distribution Approach, sampling surfaces for microbial, Sanitization Procedure, Viable Particulates from EU Annex 1, YEASTS AND MOLDS SURVEYS2 Comments on Environmental Monitoring (EM) – New Approach Guide

This Guideline applies to routine Environmental Monitoring (EM) activities in classified manufacturing areas for viable and non-viable particulates, aseptic area personnel gown and glove samples, and for utility systems supplying those areas, such as compressed air, process gases, clean steam and water systems ENVIRONMENTAL MONITORING (EM) PROGRAM 1.0   OBJECTIVE : This Global Quality Standard (GQS) […]

User Requirement Specification (URS) Handling SOP

Calibration, cGMP, Checklist, Doc, GLP, Maintenance Sops, Production, Protocol, QA Sop, QC Sop, Quality Control, SOPs, Stores Sops computerized software system, PLCs URS, URS Format, URS Register1 Comment on User Requirement Specification (URS) Handling SOP

Standard Operating Procedure (SOP) for Handling of User Requirement Specification (URS) for a computerized system or Instrument / Equipment. User Requirement Specification (URS) is a document that informs the software vendor / software on the users expectations from the software User Requirement Specification (URS) 1.0   PURPOSE: The purpose of this SOP is to establish procedure […]

Analytical Method Validation (AMV) Procedure / Guide

Calibration, cGMP, GLP, Microbiology, QA Sop, QC Sop, Quality Control, SOPs, Validation Accuracy, AMV, Filter paper selection study, Forced degradation, Intermediate Precision, Limit of detection (LOD), Limit of Quantitation (LOQ), Linearity, Mass Balance determination, Method precision, Range, recovery, Repeatability, Robustness, Solution Stability, Specificity, System precision, System suitability test1 Comment on Analytical Method Validation (AMV) Procedure / Guide

Standard Operating Procedure (SOP) and Guideline for Validation of Analytical Method (AMV). The objective of validation of an analytical Method (AMV) is to demonstrate that it is suitable for its intended purpose. Procedure for Analytical Method Validation (AMV) 1.0   Objective : To lay down procedure for validation of Analytical Method (AMV) to be followed in […]

Swab Test analysis of Equipment / Instrument – SOP

cGMP, Microbiology, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs, Validation Auto coater swab, FBD swab, Multi mill swab, RMG swab, Sifter swab, Swab Compression Machine, Swab on Equipment, Swab Sampling Point Location1 Comment on Swab Test analysis of Equipment / Instrument – SOP

Standard Operating Procedure (SOP & Guideline) for swab test analysis. Swab test analysis is being done to avoid chances of cross contamination from one product to another. By this method we assure that the machine / equipment is free from active ingredients of previous product. Procedure for Swab Test Analysis 1.0   Objective : To lay […]

Sampling of Packaging Materials – Procedure

cGMP, Checklist, Checklist / Formats, GLP, QC Sop, Quality Control, SOPs, Stores Sops Primary Packing Material, Sampling of PPM, Secondary Packaging Material1 Comment on Sampling of Packaging Materials – Procedure

Standard Operating Procedure (SOP) for sampling of packaging materials (i.e. Aluminum Foil Printed & Plain / Aluminum Foil Forming / PVC / PVDC / HDPE Bottle / Glass Bottle/ Cap Child Resistant /Cap Non Child Resistant / PP Cap / Catch Box / Catron / Label etc. Procedure for Sampling of Packaging Materials 1.0   Objective […]

Roller Compactor Machine – Operation & Cleaning

cGMP, Production, Production Sop, QA Sop, SOPs Compactor Machine, Roll CompactorLeave a Comment on Roller Compactor Machine – Operation & Cleaning

Standard Operating Procedure (SOP) for cleaning and operation of Alexander werk GmbH (Germany) make Roller compactor machine. Roller Compactor Machine 1.0   Purpose : The purpose of this SOP is to lay down the cleaning and operation procedure for Roller Compactor. 2.0   Scope : This SOP  is applicable for cleaning and operation of Roller compactor WP […]

Volumetric Solution – Preparation and Standardization

cGMP, GLP, QC Sop, Quality Control, SOPs 0.1M Sodium Thiosulphate, 1M Sodium Hydroxide, Ceric Ammonium Sulphate solution, Disodium Edetate solution, Iodine solution, Perchloric Acid solutionLeave a Comment on Volumetric Solution – Preparation and Standardization

Standard Operating Procedure (SOP) and Guideline for Preparation and Standardization of Volumetric Solution(s) used during analysis of Raw material and drug product at pharmaceutical quality control department. Preparation & Standardization of Volumetric Solution(s) 1.0   Objective : The purpose of this SOP is to describe a procedure for Preparation & Standardization of Volumetric solution. 2.0   Scope […]

Steam Sterilizer – Qualification & Validation Procedure

Calibration, cGMP, Micro Sop, Microbiology, QA Sop, SOPs, Sterile, Validation Autoclave validation Procedure, Biological Challenge Test, Bowie-Dick Test, D Value, Heat Distribution Studies, Heat labile physical indicator, Heat Penetration StudyLeave a Comment on Steam Sterilizer – Qualification & Validation Procedure

Standard Operating Procedure (SOP) for procedure for Validation / Qualification of Steam Sterilizer used in microbiology laboratories. Validation of Steam Sterilizer 1.0   Purpose: To lay down the procedure for Validation of Steam Sterilizers. 2.0   Scope: This Standard Operating Procedure is applicable at microbiology section of Quality Control department. 3.0   References & Annexures: References: Health Technical […]

BOD Incubator – Cleaning, Calibration, Operation

Calibration, Micro Sop, Microbiology, QA Sop, SOPs, Validation BOD Validation, Cleaning of BOD, Incubator Validation, Temperature MappingLeave a Comment on BOD Incubator – Cleaning, Calibration, Operation

Standard Operating Procedure (SOP) for Operation, Cleaning and Calibration of Newtronic make BOD Incubator used in microbiology department for analytical activity. BOD Incubator 1.0   Purpose: To lay down the procedure for Operating, Calibration and Cleaning of BOD Incubators Model No.: NEC134 RTSSI. 2.0   Scope: This Standard Operating Procedure is applicable at Microbiology section of Quality […]

« Previous 1 2 3 4 5 6 7 8 … 18 Next »

Regulatory Audit : Preparation & Handling

August 2, 2021 August 2, 2021 pharmabeginers Audit, cGMP, Checklist, Checklist / Formats, Doc, GLP, Health & Safety (EHS), IT SOP, Maintenance Sops, Micro Sop, Microbiology, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs, Stores Sops Audit Observation, Observation Compliance, Plant Audit, QC AuditLeave a Comment on Regulatory Audit : Preparation & Handling

Standard Operating Procedure (SOP) / Guideline for Preparation and Handling of Regulatory Audit (FDA Inspection) in Pharmaceutical Drug Manufacturing Plant. Handling of Regulatory Audit (FDA Inspection) 1.0   PURPOSE The purpose of this Standard Operating Procedure (SOP) is to describe the procedure for Handling the Regulatory Audit. 2.0   SCOPE This SOP shall be used as such […]

Local Area Network (LAN) Qualification Guideline

June 25, 2021 June 25, 2021 pharmabeginers Audit, cGMP, Checklist / Formats, IT SOP, Maintenance Sops, QA Sop, QC Sop, SOPs, Validation data integrity, IT Policy, LAN DQ, LAN IQ, LAN OQ, LAN PQ, LAN QualificationLeave a Comment on Local Area Network (LAN) Qualification Guideline

Standard Operating Procedure (SOP) for Local Area Network (IT Network / LAN) qualification procedure, Protocol, and related documentation. Procedure for qualification of IT network equipment’s for the fulfillment of availability of hardware as per requirement, guidance for re-qualification and to provide the procedure for numbering of network equipment. Qualification of Local Area Network (LAN) 1.0  […]

Out of Specification Result in Microbiology – Guideline

June 5, 2021 June 5, 2021 Janki Singh cGMP, Micro Sop, Microbiology, SOPs Micro OOS, Microbiology OOS, Test Result1 Comment on Out of Specification Result in Microbiology – Guideline

Standard Operating Procedure (SOP) for Handling of Out of Specification (OOS) Test Result in Microbiological Analysis. OOS results include all test results that fall outside of the specification or acceptance criteria established in drug applications, drug master files, official compendia, or by the manufacturer. Handling of (Microbiology) Out-of-Specification (OOS) Results 1.0   Purpose The objective of […]

Validation Master Plan (VMP) Preparation Guideline

May 28, 2021 May 28, 2021 pharmabeginers cGMP, Maintenance Sops, Micro Sop, Microbiology, Production, Production Sop, QA Sop, SOPs, Validation AMV, PV, VMP-CV2 Comments on Validation Master Plan (VMP) Preparation Guideline

Standard Operating Procedure & Guideline for preparation and control of Validation Master Plan (VMP) for Instrument, Equipment, Facility in the pharmaceutical drug manufacturing plant. SOP for Validation Master Plan (VMP) 1.0   PURPOSE The purpose of this SOP is to lay down the procedure of preparation and control of the Validation Master Plan (VMP). 2.0   SCOPE […]

Technical Agreement – Preparation & Handling

May 5, 2021 May 5, 2021 pharmabeginers Audit, cGMP, Health & Safety (EHS), Maintenance Sops, Micro Sop, Microbiology, Production, Production Sop, QA Sop, QC Sop, SOPs, Stores Sops Agreement, Contract Lab, Contract PermissionLeave a Comment on Technical Agreement – Preparation & Handling

Standard Operating Procedure for preparation and handling of different types of Technical Agreement. Agreement undertook by written and legally binding on two parties (Contract giver and contract acceptor). Technical Agreement 1.0   PURPOSE: The purpose of this SOP (Standard Operating Procedure) is to describe the procedure for the preparation and handling of all technical agreement (s). […]

Infrastructure Qualification Procedure – Quality IT

April 12, 2021 April 9, 2021 pharmabeginers Audit, Calibration, cGMP, GLP, QA Sop, QC Sop, Quality Control, SOPs, Validation Computer system validationLeave a Comment on Infrastructure Qualification Procedure – Quality IT

Standard Operating Procedure (SOP) for IT Infrastructure Qualification of Computer System used in cGxP environment at the pharmaceutical company. Computer System – IT Infrastructure Qualification 1.0   Objective  This Procedure defines the procedure for qualifying and maintaining the qualified status (Qualification) of Computerized Systems (CS) Infrastructure to ensure that Computerized Systems that use that infrastructure and […]

Placebo Medicine Batch – Procedure for Handling

April 7, 2021 April 7, 2021 pharmabeginers cGMP, GLP, Production, Production Sop, QC Sop, Quality Control, SOPs Placebo ProductLeave a Comment on Placebo Medicine Batch – Procedure for Handling

A placebo batch of a product is processed as per regular formulation of that product except for the active ingredient or A dosage form that is identical to the drug product except that the drug substance is absent or replaced by an inert ingredient or a mixture of the drug product excipients quantitatively equivalent to […]

Audit Checklist – Department wise in Pharmaceuticals

March 17, 2021 March 17, 2021 pharmabeginers cGMP, Checklist, Checklist / Formats, Environment, Health & Safety (EHS), Micro Sop, Microbiology, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs, Stores Sops Inspection ChecklistLeave a Comment on Audit Checklist – Department wise in Pharmaceuticals

Audit Checklist (s) for different department/section/area like – Engineering / maintenance, HVAC Area, Purified water system, Quality Control, Warehouse, Granulation, Compression, Coating, Packing / Packaging, Personal and administration (HR), Microbiology and Quality Assurance area etc. to check the effectiveness  of the implemented systems. Checklist for Routine Inspection /Audit 1.0   Audit checklist for Engineering area Sr. […]

Rejection Handling Procedure (API/Drug Product)

February 27, 2021 March 1, 2021 pharmabeginers cGMP, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs Rejected APILeave a Comment on Rejection Handling Procedure (API/Drug Product)

Standard Operating Procedure (SOP) for Handling of Interim/On-line Rejection during manufacturing and packing of drug substances or drug product. Handling of Interim/On-line Rejection 1.0   Purpose : To define procedure for Handling of Interim/On-line Rejections during manufacturing and packing of drug substances. 2.0   Scope : This SOP is applicable for Handling of Interim/On-line Rejections during manufacturing […]

Gram’s Staining Procedure of Microorganisms

February 20, 2021 February 13, 2021 pharmabeginers cGMP, Environment, GLP, Health & Safety (EHS), Micro Sop, Microbiology, QC Sop, Quality Control, SOPs, Sterile Lacto Phenol Staining, Spore StainingLeave a Comment on Gram’s Staining Procedure of Microorganisms

Standard Operating Procedure (SOP) for Gram’s Staining of Microorganisms. Gram stain or Gram staining, also called Gram’s method, is a method of staining used to distinguish and classify bacterial species into two large groups: gram-positive bacteria and gram-negative bacteria. The name comes from the Danish bacteriologist Hans Christian Gram, who developed the technique Procedure for […]

Incident Handling and Investigation Procedure – EHS

February 17, 2021 February 13, 2021 pharmabeginers cGMP, Environment, Health & Safety (EHS), Production, QA Sop, QC Sop, SOPs, Stores Sops Accident, Dangerous Occurrences, Environmental Incidents, Fatal Incident, Fire Incidents, First Aid Incident, Incident, Near Miss, Occupational IllnessLeave a Comment on Incident Handling and Investigation Procedure – EHS

Standard Operating Procedure (SOP) for Handling, Investigation, Classification and Reporting of Incident by Environmental,  Health and Safety (EHS) department in pharmaceuticals. Incident Investigation, Classification and Reporting (EHS) 1.0   PURPOSE: To laydown a procedure to describe the incident, its classification, the requirement of investigation and its reporting procedure by Environment, Health and Safety Department (EHS). The […]

Programmable Logic Controller (PLC) Qualification

February 10, 2021 February 9, 2021 pharmabeginers Calibration, cGMP, Checklist, Maintenance Sops, Production, Production Sop, Protocol, QA Sop, Validation HDMI, PLC Calibration, PLC Validation1 Comment on Programmable Logic Controller (PLC) Qualification

Protocol and Procedure for Installation Qualification of Programmable Logic Controller (PLC) connected with Manufacturing Equipment. Installation Qualification of Programmable Logic Controller (PLC) 1.0   Objective : The objective of this protocol to provide the written guidelines for execution of the installation qualification of Programmable Logic Controller (PLC) based HMI System for ________ Define the installation qualification […]

« Previous 1 2 3 4 5 6 7 8 … 23 Next »

Regulatory Audit : Preparation & Handling

August 2, 2021 August 2, 2021 pharmabeginers Audit, cGMP, Checklist, Checklist / Formats, Doc, GLP, Health & Safety (EHS), IT SOP, Maintenance Sops, Micro Sop, Microbiology, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs, Stores Sops Audit Observation, Observation Compliance, Plant Audit, QC AuditLeave a Comment on Regulatory Audit : Preparation & Handling

Standard Operating Procedure (SOP) / Guideline for Preparation and Handling of Regulatory Audit (FDA Inspection) in Pharmaceutical Drug Manufacturing Plant. Handling of Regulatory Audit (FDA Inspection) 1.0   PURPOSE The purpose of this Standard Operating Procedure (SOP) is to describe the procedure for Handling the Regulatory Audit. 2.0   SCOPE This SOP shall be used as such […]

Local Area Network (LAN) Qualification Guideline

June 25, 2021 June 25, 2021 pharmabeginers Audit, cGMP, Checklist / Formats, IT SOP, Maintenance Sops, QA Sop, QC Sop, SOPs, Validation data integrity, IT Policy, LAN DQ, LAN IQ, LAN OQ, LAN PQ, LAN QualificationLeave a Comment on Local Area Network (LAN) Qualification Guideline

Standard Operating Procedure (SOP) for Local Area Network (IT Network / LAN) qualification procedure, Protocol, and related documentation. Procedure for qualification of IT network equipment’s for the fulfillment of availability of hardware as per requirement, guidance for re-qualification and to provide the procedure for numbering of network equipment. Qualification of Local Area Network (LAN) 1.0  […]

Out of Specification Result in Microbiology – Guideline

June 5, 2021 June 5, 2021 Janki Singh cGMP, Micro Sop, Microbiology, SOPs Micro OOS, Microbiology OOS, Test Result1 Comment on Out of Specification Result in Microbiology – Guideline

Standard Operating Procedure (SOP) for Handling of Out of Specification (OOS) Test Result in Microbiological Analysis. OOS results include all test results that fall outside of the specification or acceptance criteria established in drug applications, drug master files, official compendia, or by the manufacturer. Handling of (Microbiology) Out-of-Specification (OOS) Results 1.0   Purpose The objective of […]

Validation Master Plan (VMP) Preparation Guideline

May 28, 2021 May 28, 2021 pharmabeginers cGMP, Maintenance Sops, Micro Sop, Microbiology, Production, Production Sop, QA Sop, SOPs, Validation AMV, PV, VMP-CV2 Comments on Validation Master Plan (VMP) Preparation Guideline

Standard Operating Procedure & Guideline for preparation and control of Validation Master Plan (VMP) for Instrument, Equipment, Facility in the pharmaceutical drug manufacturing plant. SOP for Validation Master Plan (VMP) 1.0   PURPOSE The purpose of this SOP is to lay down the procedure of preparation and control of the Validation Master Plan (VMP). 2.0   SCOPE […]

Technical Agreement – Preparation & Handling

May 5, 2021 May 5, 2021 pharmabeginers Audit, cGMP, Health & Safety (EHS), Maintenance Sops, Micro Sop, Microbiology, Production, Production Sop, QA Sop, QC Sop, SOPs, Stores Sops Agreement, Contract Lab, Contract PermissionLeave a Comment on Technical Agreement – Preparation & Handling

Standard Operating Procedure for preparation and handling of different types of Technical Agreement. Agreement undertook by written and legally binding on two parties (Contract giver and contract acceptor). Technical Agreement 1.0   PURPOSE: The purpose of this SOP (Standard Operating Procedure) is to describe the procedure for the preparation and handling of all technical agreement (s). […]

Infrastructure Qualification Procedure – Quality IT

April 12, 2021 April 9, 2021 pharmabeginers Audit, Calibration, cGMP, GLP, QA Sop, QC Sop, Quality Control, SOPs, Validation Computer system validationLeave a Comment on Infrastructure Qualification Procedure – Quality IT

Standard Operating Procedure (SOP) for IT Infrastructure Qualification of Computer System used in cGxP environment at the pharmaceutical company. Computer System – IT Infrastructure Qualification 1.0   Objective  This Procedure defines the procedure for qualifying and maintaining the qualified status (Qualification) of Computerized Systems (CS) Infrastructure to ensure that Computerized Systems that use that infrastructure and […]

Placebo Medicine Batch – Procedure for Handling

April 7, 2021 April 7, 2021 pharmabeginers cGMP, GLP, Production, Production Sop, QC Sop, Quality Control, SOPs Placebo ProductLeave a Comment on Placebo Medicine Batch – Procedure for Handling

A placebo batch of a product is processed as per regular formulation of that product except for the active ingredient or A dosage form that is identical to the drug product except that the drug substance is absent or replaced by an inert ingredient or a mixture of the drug product excipients quantitatively equivalent to […]

Audit Checklist – Department wise in Pharmaceuticals

March 17, 2021 March 17, 2021 pharmabeginers cGMP, Checklist, Checklist / Formats, Environment, Health & Safety (EHS), Micro Sop, Microbiology, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs, Stores Sops Inspection ChecklistLeave a Comment on Audit Checklist – Department wise in Pharmaceuticals

Audit Checklist (s) for different department/section/area like – Engineering / maintenance, HVAC Area, Purified water system, Quality Control, Warehouse, Granulation, Compression, Coating, Packing / Packaging, Personal and administration (HR), Microbiology and Quality Assurance area etc. to check the effectiveness  of the implemented systems. Checklist for Routine Inspection /Audit 1.0   Audit checklist for Engineering area Sr. […]

Rejection Handling Procedure (API/Drug Product)

February 27, 2021 March 1, 2021 pharmabeginers cGMP, Production, Production Sop, QA Sop, QC Sop, Quality Control, SOPs Rejected APILeave a Comment on Rejection Handling Procedure (API/Drug Product)

Standard Operating Procedure (SOP) for Handling of Interim/On-line Rejection during manufacturing and packing of drug substances or drug product. Handling of Interim/On-line Rejection 1.0   Purpose : To define procedure for Handling of Interim/On-line Rejections during manufacturing and packing of drug substances. 2.0   Scope : This SOP is applicable for Handling of Interim/On-line Rejections during manufacturing […]

Gram’s Staining Procedure of Microorganisms

February 20, 2021 February 13, 2021 pharmabeginers cGMP, Environment, GLP, Health & Safety (EHS), Micro Sop, Microbiology, QC Sop, Quality Control, SOPs, Sterile Lacto Phenol Staining, Spore StainingLeave a Comment on Gram’s Staining Procedure of Microorganisms

Standard Operating Procedure (SOP) for Gram’s Staining of Microorganisms. Gram stain or Gram staining, also called Gram’s method, is a method of staining used to distinguish and classify bacterial species into two large groups: gram-positive bacteria and gram-negative bacteria. The name comes from the Danish bacteriologist Hans Christian Gram, who developed the technique Procedure for […]

Incident Handling and Investigation Procedure – EHS

February 17, 2021 February 13, 2021 pharmabeginers cGMP, Environment, Health & Safety (EHS), Production, QA Sop, QC Sop, SOPs, Stores Sops Accident, Dangerous Occurrences, Environmental Incidents, Fatal Incident, Fire Incidents, First Aid Incident, Incident, Near Miss, Occupational IllnessLeave a Comment on Incident Handling and Investigation Procedure – EHS

Standard Operating Procedure (SOP) for Handling, Investigation, Classification and Reporting of Incident by Environmental,  Health and Safety (EHS) department in pharmaceuticals. Incident Investigation, Classification and Reporting (EHS) 1.0   PURPOSE: To laydown a procedure to describe the incident, its classification, the requirement of investigation and its reporting procedure by Environment, Health and Safety Department (EHS). The […]

Programmable Logic Controller (PLC) Qualification

February 10, 2021 February 9, 2021 pharmabeginers Calibration, cGMP, Checklist, Maintenance Sops, Production, Production Sop, Protocol, QA Sop, Validation HDMI, PLC Calibration, PLC Validation1 Comment on Programmable Logic Controller (PLC) Qualification

Protocol and Procedure for Installation Qualification of Programmable Logic Controller (PLC) connected with Manufacturing Equipment. Installation Qualification of Programmable Logic Controller (PLC) 1.0   Objective : The objective of this protocol to provide the written guidelines for execution of the installation qualification of Programmable Logic Controller (PLC) based HMI System for ________ Define the installation qualification […]

« Previous 1 2 3 4 5 6 7 8 … 23 Next »

About the author

Ms. Janki Singh is professional pharmaceuticals blogger, Founder and Author of Pharma Beginners. She has rich experience in pharmaceutical field. Email: [email protected]

Subscribe Us

Popular Categories

Categories
Audit Blog Calibration cGMP Checklist Checklist / Formats Doc Environment GC GLP Health & Safety (EHS) HPLC IT SOP Maintenance Sops Microbiology Micro Sop Pharmacovigilance Production Production Sop Protocol QA Sop QC Sop Quality Control Research SOPs Sterile Stores Sops Uncategorized Validation

Follow Pharma Beginners

Facebook Twitter Instagram Pinterest

Recent Post

  • Vendor Evaluation Checklist (Raw Material)
    April 2, 2025/
    0 Comments
  • Batch Production Record Review Procedure
    February 20, 2025/
    0 Comments
  • Master Formula Record (MFR) & Bill of Material (BOM) – Pharma
    October 29, 2024/
    1 Comment
  • Site Acceptance Test (SAT) of Equipment
    September 5, 2024/
    0 Comments
  • Pharmaceutical CMO Selection & Qualification
    August 9, 2024/
    0 Comments
  • Lean Six Sigma Concept and Implementation
    August 5, 2024/
    0 Comments

Recent Posts

  • Vendor Evaluation Checklist (Raw Material)
  • Batch Production Record Review Procedure
  • Master Formula Record (MFR) & Bill of Material (BOM) – Pharma
  • Site Acceptance Test (SAT) of Equipment
  • Pharmaceutical CMO Selection & Qualification

Follow Us

  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab
  • Opens in a new tab

Get the Documents

To get the documents (Paid), Please contact us - [email protected] /[email protected] whatsapp - +91-9002009126
© Copyright - Pharma Beginners designed by Gosensing
error: Content is protected !!