SOP for Assigning of Numbers for Qualification Documents, Protocols and Reports

SOP for Assigning of Numbers for Qualification Documents, Protocols and Reports Objective : To lay down a procedure for assigning of number for qualification documents, protocols and reports. Scope : This Standard Operating Procedure is applicable for assigning of number for various qualification documents, protocols (validation protocols, various study protocols like stability studies, etc.) and the reports … Read more

SOP for Assigning Master Formula Card Number, Master Formula Number and Packaging Formula Number to the Drug Products

SOP for Assigning Master Formula Card Number, Master Formula Number and Packaging Formula Number to the Drug Products Objective : To lay down a procedure for assigning number to Master Formula Card, Master Formula and Packaging Formula of a Drug Product. Scope :  This Standard Operating Procedure is applicable for assigning Master Formula Card Number, Master … Read more

SOP for Assigning of Identification Numbers to Equipments, Sub-Equipments and In-process SS Items

SOP for Assigning of Identification Numbers to Equipments, Sub-Equipments and In-process SS Items Objective : To lay down a procedure for Assigning of Identification Numbers to Equipments, Sub-Equipments and In-process SS items in various departments. Scope : This Standard Operating Procedure is applicable to various departments of formulation plant. Responsibility : Head of departments or his / … Read more

SOP for Control of Stamps in Quality Assurance Department

SOP for Control of Stamps in Quality Assurance Department Objective : To lay down a procedure for Control of Stamps in Quality Assurance department. Scope :  This standard operating procedure is applicable to formulation plant. Responsibility : Officer/Executive QA shall be responsible for implementation of procedure as per this SOP. Head QA/ designee shall be responsible … Read more

SOP for Preparation of Validation and Qualification protocols

SOP for Preparation of Validation and Qualification protocols Objective : To lay down a procedure for Preparation of Validation and Qualification protocols applicable to all aspects of manufacturing processes, equipments, control systems (including computer hardware and software), utilities, facility, temperature mapping, Shipping and any significant changes to the above mentioned elements which may affect the … Read more

SOP for Access control system numbering and usage

SOP for Access control system numbering and usage Objective : To lay down a procedure for assigning of identification numbers to access control system and usage of the system. Scope : This Standard Operating Procedure is applicable to various departments of formulation plant. Responsibility : Head-User department shall be responsible for sending the request to QA department … Read more

SOP for Code to Code Transfer of Materials and Additional Testing of Materials / Products

SOP for Code to Code Transfer of Materials and Additional Testing of Materials / Products Objective : To lay down a procedure for code transfer of same material from one code to another and to carry out additional testing of APIs, Excipients and Drug Products to comply with other specifications or Pharmacopoeia. Scope : This standard operating … Read more

SOP FOR ELECTRONIC DATA BACKUP MANAGEMENT SYSTEM

SOP FOR ELECTRONIC DATA BACKUP MANAGEMENT SYSTEM Objective : To lay down a procedure for electronic data backup management system. Scope : This standard operating procedure is applicable at IT department. Responsibility : IT personnel shall be responsible for taking the backup. IT personnel shall be responsible for retrieving the tapes form other location. Officer/Executive IT shall … Read more

SOP for Procedure for Operation of SAP system in Quality Assurance Department

SOP for Procedure for Operation of SAP system in Quality Assurance Department Objective : To lay down a procedure for Operation of SAP system for in Quality Assurance Department. Scope : This SOP is applicable for production of the formulation plant. Responsibility : Head-QA/ Designee shall be responsible for releasing the Finished Goods as per this SOP. … Read more

SOP for Recording of Specimen Signatures

SOP for Recording of Specimen Signatures Objective : To lay down a procedure for recording specimen signatures of all employees. Scope : This procedure is applicable for formulation plant. Responsibility : Head HRD or his/ her designee shall be responsible for recording specimen signatures before induction training is imparted to all newly recruited employees. HODs of … Read more