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All Products QMS-135 USD 10 QMS-045 USD 7 QMS-005 USD 4 QMS-035 USD 7 QMS-015 USD 7 QMS-090 USD 8 QMS-095 USD 6 QMS-080 USD 8 QMS-055 USD 7 QMS-010 USD 7 QMS-050 USD 6 QMS-115 USD 7 QMS-085 USD 6 QMS-120 USD 6 QMS-030 USD 7 QMS-025 USD 7 QMS-020 USD 4 QMS-060 USD 7 QMS-075 USD 5 QMS-125 USD 8 QMS-110 USD 7 QMS-105 USD 7 QMS-065 USD 7 QMS-100 USD 5 QMS-070 USD 3 QMS-130 USD 5

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QMS-135 Quality Risk Management Techniques

QMS-045 Vendor Selection and Evaluation Procedure

QMS-005 How to Write Standard Operating Procedure

QMS-035 Pharmaceutical Deviation Report System

QMS-015 GMP Quality Documentation Management and Change Control

QMS-090 Evaluation of Batch Documentation and Release for Sale

QMS-095 GMP Training Procedure

QMS-080 GMP Audit Procedures

QMS-055 Pharmaceutical Product Complaint Procedure

QMS-010 All Documents - Classification, Definition and Approval Matrix

QMS-050 Vendor Certification Procedure

QMS-115 Criteria for Sourcing of Raw Materials, Packaging Components & Imported Finished Goods

QMS-085 Example of Checklist for Batch Documentation

QMS-120 Quality Concern Investigation Process

QMS-030 Preparation, Maintenance and Change Control of Master Documents

QMS-025 GMP Quality Documentation - Control, Tracking and Distribution

QMS-020 Documentation Rule for GMP Documents

QMS-060 Annual Product Review

QMS-075 Procedure for Product Identification and Traceability

QMS-125 Change Management System

QMS-110 Management and Control of Contract Work

QMS-105 House Keeping Audit Procedure

QMS-065 Manufacturing Rework Procedure

QMS-100 How to Write GMP Training Materials

QMS-070 Responsibility of Authorized Person

QMS-130 Cross Functional Investigation

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