Pharmaceutical Guidance Complete Pharma Solution
OBJECTIVE: To design, engineer and supply the Gelatin Colour Mixer and to provide assurance that …
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4 weeks ago
Design Qualification of Gelatin Colour Mixer
OBJECTIVE: To design, engineer and supply the Gelatin Colour Mixer and to provide assurance that the…
March 9, 2021
SOP for operation of Strip Packing Machine
SOP for operation of Strip Packing Machine Standard Operating Procedure (SOP) Objective To lay down …
March 8, 2021
Installation Qualification of Gelatin Storage Vessel
PURPOSE: To describe the Installation Qualification of Gelatin Storage Vessel its accessories and to…
March 7, 2021
SOP for operation of de-dusting and polishing machine
SOP for operation of de-dusting and polishing machine Standard Operating Procedure (SOP) Objective T…
March 7, 2021
SOP on operation of Paste Kettle
SOP on operation of Paste Kettle Standard Operating Procedure (SOP) Objective To lay down the proced…
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All Post URL of Drugs formulations
All Post URL of Drugs formulations Tablets MFR of Albendazole Tablets – (drugsformulations.com) MFR of …
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List of Documents required for Store/warehouse (GMP Compliances)
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SOP to prevent the spread of COVID 19 infection at workplace
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Rejection of Packaging Materials
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Reconciliation of raw materials & packaging materials
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All Post URL of Drugs formulations
All Post URL of Drugs formulations Tablets MFR of Albendazole Tablets – (drugsformulations.com) MFR of …
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VALIDATION OF HVAC SYSTEM
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Installation Qualification of Gelatin Storage Vessel
PURPOSE: To describe the Installation Qualification of Gelatin Storage Vessel its accessories and to define …
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All Post URL of Drugs formulations
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INSTALLATION QUALIFICATION PROTOCOL FOR AIR HANDLING UNIT
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Installation qualification for purified water generation system
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Installation Qualification of Vertical Laminar Reverse Flow Containment Station
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All Post URL of Drugs formulations
All Post URL of Drugs formulations Tablets MFR of Albendazole Tablets – (drugsformulations.com) MFR of …
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List of Documents required for Store/warehouse (GMP Compliances)
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SOP to prevent the spread of COVID 19 infection at workplace
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Rejection of Packaging Materials
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Reconciliation of raw materials & packaging materials
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Receiving and storages of finished goods from production area
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Receive the materials returned from production department
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Operation of dispensing booth
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Issue of additional Raw and Packaging materials
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Issuance of Raw material and Cleaning of Dispensing Booths, Dispensing Tools & Dispensing Area
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Issuance of packaging materials and transfer of issued materials from warehouse to production area
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Handling of Raw & Packaging Materials under Re-Test due
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Handling of Obsolete Rejected and on line rejections of raw materials
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Dispensing of Solvent Liquid Materials
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Dispatch of Finished Goods
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Receiving the raw materials and packaging materials
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All Post URL of Drugs formulations
All Post URL of Drugs formulations Tablets MFR of Albendazole Tablets – (drugsformulations.com) MFR of …
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List of Essential Medicines
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PROTEINS & TYPES OF PROTEINS
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USFDA GUIDELINE FOR DRUG QUALITY SAMPLING AND TESTING (DQST)- HUMAN DRUGS
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Spoken English Guru Chart
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High-Stress Jobs may lead to Early Death: Study
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Comprehensive Data Manipulation: New FDA Warning Letter for European Medicinal Product Manufacturer
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Opportunities for Reducing Sampling and Testing of Starting Materials
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Generics: FDA´s New Guidance on Prior Approval Supplements
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FDA: Updated CDER List for 2016 Guidance Documents
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Principles of HVAC Duct Design in Pharma Industry
Principles of HVAC Duct Design in Pharma Industry How Does a Duct System Work The …
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PREVENTIVE MAINTENANCE OF PRODUCTION EQUIPMENT
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All Post URL of Drugs formulations
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DESIGN QUALIFICATION FOR PURIFIED WATER STORAGE & DISTRIBUTION SYSTEM
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SOP on Operation of Effluent Treatment Plant
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Equipment in Pharma company as per USFDA
Equipment in Pharma company as per USFDA Equipment design, size, and location (§ 211.63) in …
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Production and Process Controls in Pharma industry as per USFDA
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Definitions as per 21 CFR 210 (USFDA) in Pharma company
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Buildings and Facilities in pharma industry as per USFDA
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Guideline for Hold-Time Studies of Tablets
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Equipment in Pharma company as per USFDA
Equipment in Pharma company as per USFDA Equipment design, size, and location (§ 211.63) in …
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Production and Process Controls in Pharma industry as per USFDA
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Definitions as per 21 CFR 210 (USFDA) in Pharma company
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Buildings and Facilities in pharma industry as per USFDA
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Guideline for Hold-Time Studies of Tablets
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Design Qualification of Gelatin Colour Mixer
OBJECTIVE: To design, engineer and supply the Gelatin Colour Mixer and to provide assurance that …
Read More » -
All Post URL of Drugs formulations
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Design Qualification of Gelatin Storage Vessel
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List of Documents required for Store/warehouse (GMP Compliances)
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SOP to prevent the spread of COVID 19 infection at workplace
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Design Qualification of Gelatin Colour Mixer
OBJECTIVE: To design, engineer and supply the Gelatin Colour Mixer and to provide assurance that …
Read More » -
Installation Qualification of Gelatin Storage Vessel
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Principles of HVAC Duct Design in Pharma Industry
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Process Validation: General Principles (USFDA) in Pharma Industry
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Establishment of a Control Procedure for Technical Equipment, including related Utilities, Computerized Systems and Facilities used in the Manufacture of Pharmaceuticals
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SOP FOR STABILITY STUDY IN PHARMA INDUSTRY
SOP FOR STABILITY STUDY IN PHARMA INDUSTRY OBJECTIVE: To lay down the procedure for collection, …
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Total Organic Carbon in Water in Pharma Industry
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Effectiveness of Antimicrobial Preservatives in Pharma industry
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Document Management System in Quality Assurance Department in Pharma Industry
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Management Review
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Total Organic Carbon in Water in Pharma Industry
Total Organic Carbon in Water in Pharma Industry This method for determining total organic carbon …
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Analytical Method Validation protocol
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CLINICAL TRIAL PROTOCOL
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All Post URL of Drugs formulations
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UV LAMP EFFICACY TEST