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VAL MANUAL- 013 Cleaning and Cleaning Validation of API Plant and Equipment

USD 7.00

VAL MANUAL- 001 The Preparation of Validation Master Plan

USD 6.00

VAL MANUAL- 010 Batch Homogeneity Demonstration of Active Pharmaceutical Ingredient Preparation

USD 6.00

VAL MANUAL- 044 Documenting IQ, OQ, PQ Protocol Test Results for Equipment, Facility and Computer

USD 6.00

VAL MANUAL- 011 Documentation Models for Continuous Quality Verification

USD 6.00

VAL MANUAL- 036 Information Technology Infrastructure Qualification

USD 6.00

VAL MANUAL- 006 Evaluation of Changes for Potential Impact on Process Validation

USD 6.00

VAL MANUAL- 025 Periodic Review Process of Validated Equipment and Computer Systems in Pharmaceutical Industry

USD 6.00

VAL MANUAL- 054 Procedure for Identification and Sampling of Swab and Visual Inspection Locations for Medicinal Products and API Equipment

USD 6.00

VAL MANUAL- 016 Sterilization Process Validation

USD 7.00

VAL MANUAL- 008 In-Process and Bulk Drug Product Holding Times

USD 6.00

VAL MANUAL- 004 Evaluating Non-Cleaned Equipment Hold Times for Cleaning Validation Medicinal Products

USD 6.00

VAL MANUAL- 020 Process Validation Sampling Practices for Non-Sterile Liquid and Semi Solid Drug Products

USD 6.00

VAL MANUAL- 019 Cleaning and Cleaning Validation For Formulated Products

USD 6.00

VAL MANUAL- 022 Process Validation Sampling for Non-Sterile Solid Dose Drug Products

USD 6.00

VAL MANUAL- 005 Process Validation of Bulk Drug (API and Intermediate)

USD 6.00

VAL MANUAL- 023 Performance Qualification versus Process Validation

USD 4.00

VAL MANUAL- 050 Systems Validation

USD 6.00

VAL MANUAL- 041 Clean Pure Steam System Commissioning and Qualification Approaches & Sampling Plans

USD 7.00

VAL MANUAL- 017 Matrices and Bracketing of Medicinal Products in Process Validation

USD 6.00

VAL MANUAL- 048 Purified Water and Water for Injection System Commissioning and Qualification Sampling Plans

USD 6.00

VAL MANUAL- 045 Access by Regulatory Authorities and Auditors to Electronic Records

USD 6.00

VAL MANUAL- 058 Documentation and Records for Cleaning Activities and Evaluation

USD 6.00

VAL MANUAL- 059 Identifying Critical Process Parameters for Manufacturing of Medicinal Products

USD 7.00

VAL MANUAL- 021 Principle and Precedures of Analytical Test Method Validation for GMP Regulated Industry

USD 7.00

VAL MANUAL- 028 The validation of facilities and system

USD 7.00

VAL MANUAL- 009 Process Validation for Formulated Products

USD 6.00

VAL MANUAL- 002 Clean Equipment Hold Times Establishment and Practices

USD 6.00

VAL MANUAL- 038 Validation Considerations for Transportation of Biopharmaceutical Materials

USD 6.00

VAL MANUAL- 049 Quality Considerations for Direct Impact Compressed Air and Nitrogen Systems

USD 6.00

VAL MANUAL- 018 Potential Critical Packaging Process Parameters and Validation Practices

USD 6.00

VAL MANUAL- 043 Cycle Validation for Freeze Drying

USD 6.00

VAL MANUAL- 024 General Outline of Analytical Procedure Validation

USD 4.00

VAL MANUAL- 040 Management of Change in Computerised System

USD 7.00

VAL MANUAL- 030 Identification and Investigation of Test Deviations During Validation

USD 6.00

VAL MANUAL- 031 Validation Activities during Technology Transfers

USD 6.00

VAL MANUAL- 039 System Level Impact Assessment for Information Systems

USD 7.00

VAL MANUAL- 027 Potential Critical Parameters for ProcessIinvolves in Formulating Solid Oral Dosage Forms

USD 6.00

VAL MANUAL- 053 Calculations of Residue Limits for Medicinal Product for Equipment Cleaning During Cleaning Validation

USD 7.00

VAL MANUAL- 007 Swab and Visual Inspection Sampling Locations Guidance for Process Equipment

USD 4.00

VAL MANUAL- 056 Rinsate and Swab Sampling Procedure in Test Method Development and Validation

USD 6.00

VAL MANUAL- 037 How to Investigate Unknown Chromatographic Peaks during Cleaning Validation Activity

USD 4.00

VAL MANUAL- 033 Validation Documentation

USD 6.00

VAL MANUAL- 014 Guidance on Selection Criteria of Dose and Toxicity Data

USD 6.00

VAL MANUAL- 047 Packaging Process Documentation Transfer for Drug Products

USD 5.00

VAL MANUAL- 042 Component Level Impact Assessment for Information System Application

USD 7.00

VAL MANUAL- 015 Inspection Attributes in Packaging Validation of Non-Sterile Drug Products

USD 6.00

VAL MANUAL- 055 How to Group Product and Equipment and Select the Worst Case Product in Cleaning Validation

USD 6.00

VAL MANUAL- 057 Method of Visual Inspection and Quantitation in Cleaning Validation

USD 6.00

VAL MANUAL- 060 Process Validation Approaches for Formulated Medicinal Products and Medical Devices

USD 6.00

VAL MANUAL- 035 Non-Sterile API Manufacturing Area Environmental Control

USD 5.00

VAL MANUAL- 026 Critical Parameters for Process Involves in Formulating Semi-Solid Dosage Forms

USD 5.00

VAL MANUAL- 032 Validation Considerations for Re-work and Re-process of API

USD 6.00

VAL MANUAL- 051 Implementation of Process Analytical Technology

USD 5.00

VAL MANUAL- 052 Validation of Process Analytical Technology System

USD 6.00

VAL MANUAL- 012 Documentation to Foster Continuous Quality Verification

USD 6.00

VAL MANUAL- 046 Material of Construction Documentation

USD 6.00

VAL MANUAL- 029 Examples and Approaches of Solvent Recovery Validation

USD 6.00

VAL MANUAL- 003 Equivalency Comparison of Medicinal Product Validation Batch Data to Reference Batches

USD 6.00

VAL MANUAL- 034 Demonstration and Calculation of Equivalence Criteria of Impurities for API Process Validation

USD 6.00

VAL MANUAL- 062 Use of Process Analytical Technology in Process Validation

USD 6.00

VAL MANUAL- 061 Cleaning Validation and Verification of Equipments Used for Manufacturing Active Pharmaceutical Ingredients

USD 7.00
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