SOP for Resuming Aseptic Area after Maintenance Activities : Pharmaceutical Guidelines

Editable Pharmaceutical Documents in MS-Word Format

View

8

SOP for Resuming Aseptic Area after Maintenance Activities

Standard operating procedure to resume activities in the sterile manufacturing area after maintenance work.

1.0 OBJECTIVE

To lay down a procedure for resuming aseptic area after maintenance activities.

2.0 SCOPE

This procedure applies to sterile manufacturing facilities.

3.0 RESPONSIBILITY

Chemist/ Executive

4.0 ACCOUNTABILITY

Asst. Manager

5.0 PROCEDURE

The maintenance activities include:

5.1 Preventive maintenance

5.1.1 Schedule the planned preventive maintenance preferably for the last working shift of the week or a holiday.
5.1.2 Issue a maintenance requisition elaborating the availability of the machine.
5.1.3 During the planned preventive maintenance do not keep components in or near the area where the preventive maintenance will be carried out.
5.1.4 Ensure that the trained maintenance personnel is aware of the aseptic operations and requirements.
5.1.5 The maintenance personnel going into the aseptic area will follow the SOP of the sterile area.
5.1.6 Take care to prevent the spillage of oil, grease or any other material from falling onto the ground. (This can be prevented by placing a sanitized polythene sheet at the area of work.)
5.1.7 After the completion of the job remove the poly sheet and discard the same out of the sterile area across a hatch.
5.1.8 After removal of the sheet from the pass box, disinfect the pass box area with the solution prepared for the day.
5.1.9 Cleaning and disinfection of the area which had been under maintenance will be carried out.

5.2 Breakdown maintenance

5.2.1 With well planned preventive maintenance, the breakdown maintenance usually involves minor adjustments or alterations to ensure that process and quality parameters are within limits. However, if the breakdown is of significant nature, case the aseptic operations and follow the below-mentioned procedures.
5.2.2 Ensure the removal of product and sterilized containers from the workplace.
5.2.3 Carry out the required maintenance activities.
5.2.4 Follow steps 5.1.5 to 5.1.9
5.2.5 Take dummy trials and ensure that the product parameters of the equipment are met.
5.2.6 After taking the dummy trial, the whole related area must be clean and disinfected with scheduled disinfectant solution.
5.2.7 Spray 70% filtered (sterilized) IPA solution in area.

6.0 ABBREVIATIONS

6.1 SOP: Standard Operating Procedure
6.2 IPA: Isopropyl Alcohol
Get ready to use editable documents in MS-Word FormatView List





Ankur Choudhary is India's first professional pharmaceutical blogger, author and founder of Pharmaceutical Guidelines, a widely-read pharmaceutical blog since 2008. Sign-up for the free email updates for your daily dose of pharmaceutical tips.
.moc.enilediugamrahp@ofni :liamENeed Help: Ask Question


Click Here

No comments: Read Comment Policy ▼

Post a Comment


Popular Categories

QA SOPs QC SOPs Micro SOPs HVAC Production SOPs Stores SOPs Checklists Maintenance SOPs HPLC Sterile GLP Validation Protocols Water System GDP Regulatory Maintenance Calibration Warning Letters

Follow Pharmaguideline


DOCUMENTS

PHARMACEUTICAL DOCUMENTS




Editable Pharmaceutical Documents in MS-Word Format. Ready to use SOPs, Protocols, Master Plans, Manuals and more...

View


adsbypg

Discussion - Latest Topics

Show All ❭❭Pharmaguideline Forum



GET APP FOR NEWS UPDATES

Pharmaceutical Updates




✔ Worldwide Regulatory Updates
✔ Pharmaceutical News Updates
✔ Interview Questions and Answers
✔ All Guidelines in One Place

Install


Recent Posts