The Ultimate Resource for Pharmaceutical SOPs and Best Practices
SOP for SIP (Sterilize-in-Place) System Standard Operating Procedure for SIP System 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the SIP (Sterilize-in-Place) system in the pharmaceutical manufacturing of otic dosage forms to ensure effective and consistent sterilization of equipment. 2) Scope This SOP applies…
SOP for CIP (Clean-in-Place) System Standard Operating Procedure for CIP System 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the CIP (Clean-in-Place) system in the pharmaceutical manufacturing of otic dosage forms to ensure effective and consistent cleaning of equipment. 2) Scope This SOP applies…
SOP for Cleanroom Monitoring System Standard Operating Procedure for Cleanroom Monitoring System 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the cleanroom monitoring system in the pharmaceutical manufacturing of otic dosage forms to ensure controlled and compliant cleanroom conditions. 2) Scope This SOP applies…
SOP for HVAC System Standard Operating Procedure for HVAC System in Pharmaceutical Manufacturing 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the HVAC (Heating, Ventilation, and Air Conditioning) system in the pharmaceutical manufacturing of otic dosage forms to ensure controlled environmental conditions. 2) Scope…
SOP for Aseptic Filling Isolator Standard Operating Procedure for Using Aseptic Filling Isolator 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the aseptic filling isolator in the pharmaceutical manufacturing of otic dosage forms to ensure aseptic conditions during the filling process. 2) Scope This…
SOP for Sterility Test Isolator Standard Operating Procedure for Using Sterility Test Isolator 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the sterility test isolator in the pharmaceutical manufacturing of otic dosage forms to ensure aseptic conditions during sterility testing. 2) Scope This SOP…
SOP for Nitrogen Purging System Standard Operating Procedure for Using Nitrogen Purging System 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the nitrogen purging system in the pharmaceutical manufacturing of otic dosage forms to ensure the removal of oxygen and prevent oxidation of sensitive…
SOP for In-Process Checkweigher Standard Operating Procedure for Using In-Process Checkweigher 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the in-process checkweigher in the pharmaceutical manufacturing of otic dosage forms to ensure accurate weight measurement during the manufacturing process. 2) Scope This SOP applies…
SOP for Glove Box Standard Operating Procedure for Using Glove Box 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the glove box in the pharmaceutical manufacturing of otic dosage forms to ensure containment and protection of sensitive materials from external contaminants. 2) Scope This…
SOP for Cryogenic Mill Standard Operating Procedure for Using Cryogenic Mill 1) Purpose The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the cryogenic mill in the pharmaceutical manufacturing of otic dosage forms to ensure efficient size reduction of materials at ultra-low temperatures. 2) Scope This SOP…