SOP FOR PERSONNEL ENTRY AND EXIT PROCEDURE IN PRODUCTION OBJECTIVE: To lay down the Procedure for Entry and Exit Procedure for Staff, Visitors, worker in Secondary Change Room of Production Area. SCOPE: This procedure is applicable for Entry and Exit procedure for Staff, Visitors, worker. RESPONSIBILITY: It is the responsibility of operator and production supervisors to follow the … Read more
SOP FOR PROCEDURE FOR ENTRY AND EXIT TO THE WAREHOUSE OBJECTIVE: To lay down the procedure for entry and exit to the warehouse. SCOPE: This procedure is applicable to Opening and closing of warehouse RESPONSIBILITIES: It is the responsibility of store assistant to follow the procedure as prescribed in this SOP during entry and exit to the warehouse. … Read more
SOP FOR MANUFACTURING OPERATION START UP AND SHUT DOWN IN THE AREA OBJECTIVE: To lay down the procedure for Manufacturing Operation start up and close down the activity. SCOPE: This procedure is applicable for activities to be carried out before start up and after close down the Activity.. RESPONSIBILITY: It is the responsibility of operator and production supervisors … Read more
SOP FOR OPENING AND CLOSING OF PRODUCTION DEPARTMENT OBJECTIVE: To lay down the procedure for opening and closing of Production Department. SCOPE: This procedure is applicable to opening and closing of Production Department RESPONSIBILITY: It is the responsibility of production chemist/officer to follow the procedure prescribed in this SOP for opening and closing of Production Department. It … Read more
SOP FOR OPERATION AND CLEANING DRY SYRUP FILLING MACHINE OBJECTIVE: To lay down the procedure for operation and cleaning of dry syrup filling machine. SCOPE: This procedure is applicable for operation and cleaning of dry syrup filling machine RESPONSIBILITY: It is the responsibility of operator and production supervisors to follow the procedure as prescribed in this SOP during … Read more
SITE MASTER FILE Site Master File that is useful to the regulatory authority in planning and conducting GMP inspections. The Site Master File is prepared by the pharmaceutical manufacturer and should contain specific information about the quality management policies and activities of the site, the production and/or quality control of pharmaceutical manufacturing operations carried out … Read more
QUALITY MANUAL QUALITY MANUAL describes one comprehensive model for an effective pharmaceutical quality system that is based on the quality concepts, includes applicable Good Manufacturing Practice (GMP) regulations and complements serves as the Validation Road map, setting the course, justifying the strategy, outlining the preliminary test and acceptance criteria, and documenting the necessary programs that … Read more
DQ (DESIGN QUALIFICATION) DOCUMENT FOR AHU- 4000 CFM / 150 mm wg – SP To prepare detailed specifications (Design data) for HVAC System and its major components, to Ensure that the User Requirement Specifications, as described in RDS are achieved. To design the system in conjunction with the design data in order to provide basis for … Read more
ENVIRONMENTAL FAILURE (STEPS TO BE TAKEN IN CASE) PURPOSE: To lay down a procedure for steps to be taken in case of environmental failure. SCOPE: This SOP is applicable for steps to be taken in case of environmental failure in Dry Powder Injection section. RESPONSIBILITY: Preparation of SOPs: Officer/ Executive of Production Departments Checking and … Read more
SOP ON CAPA (CORRECTIVE ACTION AND PREVENTIVE ACTION) PURPOSE: To lay down the standard operating procedure for Corrective Action and Preventative Action (CAPA) is a system of quality procedures required to eliminate the causes of an existing nonconformity and to prevent recurrence of nonconforming product, processes, and other quality problems. SCOPE: This SOP is applicable … Read more