- SOP on Receipt of Raw Materials and Packaging Materials
- Qualification of Water System
- In-Process Checks During Blister Packaging
- Quality Audit: Introduction, Types and Procedure
- Product Recall: Introduction, Classification and Recall Strategy
- In-Process control & Inspection for the Small Volume Injectable (SVPs)
- Product Recall: Introduction, Classification and Recall Strategy
- Introduction to Water for Pharmaceutical Purpose
- Corrective and Preventive Actions…Basic approach
- Site Master File (SMF)
- Process FMECA in Pharmaceutical Manufacturing
- Hold Time Study …..current approach
- SOP on Quality Risk Management
- SOP on Failure Mode and Effect Analysis and Root cause Analysis
- Environmental Control - Air Handling Air Conditioning and Refrigeration
- Pharmaceutical Interview - Frequently Asked Questions
- Introduction to Pharmaceutical Clean Room
- Validation of HVAC System
- U.S. Food & Drug Administration - Complaints : Investigation & Review - 2017
- What is Calibration, Verification and Validation in pharmaceuticals?
- “Life cycle Approach to Process Validation” - Current Regulatory perspective & It’s Benefits
- Testing of Primary Packaging Materials
- Blinding and Re-labeling of Clinical Trial Samples for Clinical Trial purpose
- Concept of URS, DQ, IQ, OQ, PQ
- Sampling of Inprocess Materials and Finished Products
- Presentation on Hold Time Study (OSD)
- Presentation On SOP of SOP
- Presentation On Document and Data Control
- Change Control
- Untouched area of Data Integrity in Pharmaceutical Industry
- Online Test
- DCGI Makes LSSDC Certification Compulsory For All Pharma Manufacturing Jobs From 2018
- TSE & BSE Risk and Regulation in Pharmaceuticals
- SOP on Alarms
- SOP on Issuance, Preparation, Storage, Usage and Disposal of Disinfectant Solution
- SOP on Pest & Rodent Control
- SOP on Handling of Non-Conformances
- Protocol for Validation of Sterilization Process using Steam Sterilizer (Bung Processor)
- SOP on Electronic Data Backup Management System
- SOP for Management of Equipment
- SOP on Repackaging / Re-labeling of Finished Goods
- Review, Storage, Retrieve and Disposal of Executed Batch Documents
- Sop on Rejection and Destruction Policy of Drug Products and its Components
- Corrective and Preventive Action (CAPA)
- Difference Between Calibration and Validation
- URS (User Requirement Specification) Sterile API Facility
- SOP For House Keeping Personnel Movement in Manufacturing Facility
- SOP On Facility Designing and Qualification
- Bowl Fill Seal (BFS) Technology in pharmaceutical for sterile Preparation
- SOP on Status Labeling System and Its Control
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