sop for vendor approval of raw materials

sop for vendor approval of raw materials 1.0 OBJECTIVE: :  1.1 The objective of this SOP is: 1.1.1. To describe a procedure to assess the vendors who can manufacture and supply materials of consistent quality and quantity and at right time 2.0 RESPONSIBILITY: 2.1 The Head – Quality Assurance shall be: 2.1.1. Responsible for auditing … Read more

sop for handling of non conformance incidence

sop for handling of non conformance incidence   1.0. OBJECTIVE:  The objective of this SOP is: 1.1 This procedure defines the responsibilities and authority for handling and investigating non-conformance (NC), for taking appropriate corrective and preventive actions to prevent recurrence of the same. 2.0. RESPONSIBILITY: 2.1 Any employee of the organization shall be: 2.1.1 Responsible … Read more

sop for self inspection and internal audit for quality

  sop for self inspection and internal audit for quality     1.0 OBJECTIVE:   The objective of this SOP is: 1.1 To laid down the procedure to conduct self-inspection (Internal Audit) in order to monitor the implementation and compliance with Good Manufacturing Practices (GMP), Principles and to propose necessary corrective measures. 2.0 RESPONSIBILITY: 2.1 The … Read more

sop for area and equipment clearance procedure

sop for area and equipment clearance procedure   OBJECTIVE:  1.0 To describe the procedure for checking of equipment and area before giving line clearance during manufacturing and packaging operation. 2.0 RESPONSIBILITIES: 2.1 Quality Assurance – Officer/ Executive shall be: 2.1.1 Responsible for assuring the equipment and area for free from remnant of previous batch / … Read more

sop for quarantined release for warehouse

1.0 OBJECTIVE:  The objective of this SOP is: 1.1 To describe a procedure for allowing transfer of Finished Goods under “Quarantined status” to our godown. 2.0 RESPONSIBILITY: 2.1 The Head – Warehouse shall be: 2.1.1 Responsible for raising the request for Quarantined Release. 2.2 Quality Assurance Officer shall be: 2.2.1 Responsible for verification and reconciliation … Read more

sop for maintenance of equipment log book

1.0 OBJECTIVE  1.1 To describe a procedure for maintenance of equipment logbook. 2.0 SCOPE 2.1 This procedure is applicable to all equipment used in production sections . 3.0 RESPONSIBILITY 3.1 Concern Officer/Executive shall enter the operation and cleaning details in equipment log book. 3.2 Concern Officer/Executive shall execute this SOP. 4.0 ACCOUNTABILITY 4.1 Department Head … Read more

sop for qualification of outsource testing facility

1.0 OBJECTIVE  1.1 To describe a procedure for Qualification of Outsource Testing Facility. 2.0 SCOPE 2.1 This procedure is applicable to testing the outsource qualification 3.0 RESPONSIBILITY 3.1 Executive – Quality Assurance Department. 4.0 ACCOUNTABILITY 4.1 Head – Quality Assurance. 5.0 PROCEDURE 5.1 Selection criteria 5.1.1 Outsource testing facility should have approved by any regulatory … Read more

sampling testing and release of packaging material

1.0 OBJECTIVE: 1.1 To lay down the procedure for sampling, release and rejection of Packaging material 2.0 SCOPE: 2.1 This procedure is applicable for sampling, release and rejection of Packaging material 3.0 RESPONSIBILITY: 3.1 Executive/Officer/Chemist : Quality Control Department 4.0 ACCOUNTABILITY: 4.1 Head-QC (or) his designee/deputy 5.0 REFERENCE(S): 5.1 In-House 6.0 ENVIRONMENT, HEALTH AND SAFETY … Read more

packaging material corrugated box standard testing procedure

PROCEDURE: 1.0 Description: Take 1 corrugated box from each container sampled and check visually the corrugated box as per specification and record the observations. Check the colour of the box as per specification. Check for the no. of ply and check whether box is properly closed or not. 2.0 Pasting: Check the pasting of the … Read more

Analytical Method Validation Procedure

1.0 OBJECTIVE  1.1 To lay down the detailed procedure for the Validation of Analytical Methods / Procedures. 2.0 SCOPE 2.1 This Procedure is applicable for the Validation of Analytical Methods being executed using Chromatographic Systems (For Assay, Related Substances, Residual Solvents, Chromatographic Purity, and Content Uniformity etc.), Rate, Particle Size, Viscosity etc. in the Quality … Read more

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