Approval Block. Prepared by: Signature Date Evan Parnell 18 JUN Reviewed by: Signature Date. Approved by: Signature Date

Similar documents
Approval Block. Prepared by: Signature Date. Evan Parnell 18 JUN Reviewed by: Signature Date. Brian Flynn 18 JUN 2014

Approval Block. Prepared by: Signature Date. Margaret Crouse 18 JUN Reviewed by: Signature Date. Brian Flynn 18 JUN 2014

MICROBIOLOGICAL BEST LABORATORY PRACTICES USP <1117>

MODULE 2D ENVIRONMENTAL MICROBIOLOGICAL LABORATORY ACCREDITATION PROGRAM (EMLAP) ADDITIONAL REQUIREMENTS

Streamline your microbial detection workflow with the Milliflex platform.

MODULE 2D ENVIRONMENTAL MICROBIOLOGICAL LABORATORY ACCREDITATION PROGRAM (EMLAP) ADDITIONAL REQUIREMENTS

IACUC Standard Operating Procedure SOP : Isolation of Hazardous Chemicals/Agents in Use in Rodents

Sterile Compounding elearning Course Curriculum 28 lessons with 33 hours of CE. Fundamentals of Sterile Compounding (8 lessons/8 hours CE)

Streamline your microbial detection workflow with the Milliflex platform.

Environmental Monitoring of Aseptic Processing Areas - 1

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

Environmental Monitoring of Aseptic Processing Areas - 2

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

Sterile Compounding elearning Course Curriculum 28 lessons with 33 hours of CE. Fundamentals of Sterile Compounding (8 lessons/8 hours CE)

UNIVERSITY OF NEVADA LAS VEGAS BSL-2 LABORATORY STANDARD OPERATING PROCEDURES (SOPS)

Biosafety Training. WVU Shared Research Facilities 2012

STANDARD OPERATING PROCEDURE PROCEDURE NO: GLP 101 MOD: 2 nd Issue Page: 1 of 6 Procedure Type: General Laboratory Procedure

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

The ABCs and Challenges of GMP The American Experience

Animal Facility Biosafety Level 3 Checklist (date: April 16, 1998)

Microbiology Testing: USP requirements for Sterile and Nonsterile Preparations Webinar Q&A

USP Chapter 823 USP 32 (old) vs. USP 35 (new)

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

Lab Biosafety Self-Audit Form (Applies to all microbial work.)

TECHNICAL LEAFLET. MEDI-MEDIA-FILL KIT SUPPLY PACKAGE (Code: MR-25/S)

ENHANCED CONTAINMENT CL2 + (Level 3 practices in a Level 2 lab)

Course Competencies Template Form 112

Supplementary Training Modules on Good Manufacturing Practice. Validation. WHO Technical Report Series, No. 937, Annex 4.

Overview of a sterility assurance program for PET drugs

ENVIRONMENTAL HEALTH & SAFETY

Overview of Inspection Issues with Legacy Products. Barbara Breithaupt Consumer Safety Officer

MICROBIOLOGICAL ANALYSIS OF FOOD & FOOD PRODUCTS

Delaware State University

Review Validation of aseptic processes for pharmaceuticals

GUIDE TO INSPECTIONS OF MICROBIOLOGICAL PHARMACEUTICAL QUALITY CONTROL LABORATORIES

At Your ServIce. Microbiology Services. The life science business of Merck operates as MilliporeSigma in the U.S. and Canada.

Documenta tion and Records

How to Handle Excursions in Environmental Monitoring (EM) and Personnel Monitoring (PM) in an Aseptic Processing Plant

STANDARD OPERATING PROCEDURES

Contents. Contents (13) 1 Production (23)

Course Competencies Template Form 112

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

Establishing Laboratory Facilities to Tackle the Challenge of MDR & XDR TB in the Kingdom of Lesotho

Introduction and Background

Milliflex Rapid Microbiology Detection System

THE UNIVERSITY OF NEWCASTLE- DISCIPLINE OF MEDICAL BIOCHEMISTRY. STANDARD OPERATING PROCEDURE PROCEDURE NO: GLP 086 MOD: 1st Issue Page: 1 of 5

Dr. D. S. Rathore Rajasthan Pharmacy College

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

STANDARD OPERATING PROCEDURE #712 USE OF AZOXYMETHANE IN RODENTS

Webinar. The New EU-GMP Annex 1 draft Dupont. GOP-Innovations your Partner for Practical Training and e-learning. 8 June 2018

4.5 Compounding Compounding in Licensed Pharmacies.

Incremental GMPs. Presented by: Karen S. Ginsbury For: IFF October 31, Nov 02, PCI Pharmaceutical Consulting Israel Ltd.

Microbiological Methods

PHCT 401 Aseptic Processes & Techniques

Laboratory Close-Out Guidelines

Biological contamination events in isolators: What lessons can be learned?

STANDARDS FOR COMPOUNDING PHARMACIES

Actero Salmonella Enrichment Media Product Information

Microbiology Research Associates

USP <797> Compliance Common Challenges and Potential Solutions

Miltenyi Biotec CryMACS Freezing Bag Validation

DUQUESNE UNIVERSITY. Biosafety Guidelines

DUQUESNE UNIVERSITY. Biosafety Guidelines

SterilAmp II Geobacillus stearothermophilus

compounding area based on environmental sampling and cleaning product type. Antiseptics and determine the appropriate use of each.

Allergy Laboratories, Inc. 10/4/13

Inspection Checklist - Animal Pathogen Containment Level 2 Facilities

Julie Roberts. Audit hot Topics and Regulatory Requirements

Examination Content Certified Biological Safety Professional. ABSA International 2018

General European OMCL Network (GEON) QUALITY MANAGEMENT DOCUMENT

Culturing microorganisms may be hazardous

Supersedes Division Name Revision No. 0 Export Division Page No. 1 of 9

UNDER SECRETARY FOR HEALTH S INFORMATION LETTER MICROBIOLOGICAL ASSESSMENT OF PHARMACEUTICAL CLEANROOMS

When Quality Matters. Microbial Air Samplers: Selection Criteria in Biopharma Manufacturing. Celebrating Over 50 Years In Business!

Aseptic Techniques. A. Objectives. B. Before coming to lab

Section 6.6 BSL3 & ABSL3 Biocontainment

FDA s Guidance for Industry

PERFORMANCE QUALIFICATION PROTOCOL HVAC SYSTEM

Media Fill A Process Simution. Presented By Shikha Chauhan

Recent FDA Inspection Findings and Trends

BIO & PHARMA ANALYTICAL TECHNIQUES

Atlantic Technical Systems, Inc. 415 Headquarters Drive # 2 Millersville, MD USA Office: (410) Fax: (410)

White Paper. Risk Management in Environmental Monitoring: Should you be spotting it sooner?

Community Pharmacy Opening/Renovation Audit

Autoclave Use Procedures

Overview of Generic PET Applications. Sema Basaran, Ph.D. The 34 th Annual High Country Nuclear Medicine Conference.

QUALITY UPDATE Q1 2018

Good Laboratory Practice Facilities: Building and Equipment Hedwig Beernaert

LAB. Interpretation Guide. Lactic Acid Bacteria Count Plate

Tests to Support Sterility Claim. Imtiaz Ahmed

Application of Quality Risk Management Tools for Cell Therapy Manufacturing

Compounding Pharmacies and the Contract Testing Lab

New York State Department of Health - Wadsworth Center Laboratory of Environmental Biology NYS ELAP Laboratory ID 10765

Actero Salmonella/STEC Enrichment Media Product Information

Media Fill Evaluations in Cellular Therapy Product Manufacturing: Three Possible Approaches. Doug Padley Mayo Clinic

Tissue Culture Sterilization and Contamination

GUIDANCE NOTES ON ANALYTICAL METHOD VALIDATION

Post Sterilization Lab Contamination

Receiving and Storage of Cytotoxic Substances

Lessons from Pharmaceutical Laboratory related FDA Warning Letters

Transcription:

ATS-ATP-5856 Page: 1 of 5 Approval Block Prepared by: Signature Date Evan Parnell 18 JUN 2014 Reviewed by: Signature Date Brian Flynn 18 JUN 2014 Approved by: Signature Date Kristal Jewell 18 JUN 2014 Historical Reference Section: Section Name Section Number (i.e., 5.2.1) Revision Affected Explanation of Change References 3.0 A Added references Quality Control 10.0 A Added section Approval Block N/A A Added Approval Block 1. Purpose This document provides instruction for air and contact viable sample incubation and analysis for USP <1116> compliant Water For Injection (WFI) systems. 2. Scope This procedure shall be followed by personnel performing viable sample analysis. Additional testing and or deviation from this SOP shall be agreed upon prior to the start of testing.

ATS-ATP-5856 Page: 2 of 5 3. References 1. USP<1116> Pharmaceutical Compounding Sterile Preparations 2. ATS SOP 720.00 Rev (A) Standard Operating Procedure for the Operation of the NuAire Model NU-425-300 Labgard Class II, Type A2 Laminar Flow Biological Safety Cabinet 3. ATS SOP 700.00 Rev (A)Standard Operating Procedure for the Operation of the Model 3110 Forma Series II Water Jacket CO 2 Incubator 4. ATS SOP 705.00 Rev (A) Standard Operating Procedure for the Operation of the Dickson KT621 Remote Sensing Temperature Recorder 5. ATS SOP 715.00 Rev (A) Standard Operating Procedure for Scientific Revco Laboratory Refrigerator 6. ATS SOP 725.00 Rev (A) Standard Operating Procedure for the Operation of the UVP Colony Doc-It Imaging Station 7. ATS SOP 735.00 Rev (A) Standard Operating Procedure: Milliflex Plus Pump 8. ATS SOP for the Autoclave being used (SOPs 730 and 731) 9. ATS SOP 725.00 Rev (A) Standard Operating Procedure for the Operation of the UVP Colony Doc-It Imaging Station 10. ATS SOP 735.00 Rev (A) Standard Operating Procedure for the Milliflex Plus Pump 11. ATS SOP 820.00 Rev (A) Standard Operating Procedure: Viable Sample Workflow 12. ATS SOP 880.00 Rev (A) Standard Operating Procedure: Gowning Procedures 13. ATS SOP 900.00 Rev (A) Logbook Entries 14. ATS SOP 905.00 Rev (A) Standard Operating Procedure: Organization of plates in the incubator 15. ATS SOP 920.00 Rev (A) Standard Operating Procedure: Fungi Slide Preparation 16. ATS SOP 925.00 Rev (A) Standard Operating Procedure: Identification of Microorganisms 17. Quality Manual Section 4.11 18. MSDS for all relevant chemicals 4. Equipment and Materials 1. UVP Colony Doc-It Imaging Station or equivalent. 2. Milliflex PLUS Pump 3. Refrigerator 4. Incubators

ATS-ATP-5856 Page: 3 of 5 5. Safety 1. Wear proper attire as specified by SOP 880. 2. Refer to manufacturer s safety precautions and Material Safety Data Sheet (MSDS) for appropriate protective equipment and safe handling procedures when using chemicals. 6. Responsibility 1. It is the responsibility of the President to maintain this document and oversee these activities. 2. It is the responsibility of the individual(s) performing this task to follow this procedure. 7. Preliminary Operations 1. Collect all materials and equipment necessary to conduct the project. 2. Ensure all equipment is within calibration prior to the start of use. 8. Incubation and Analysis Procedures 1. If samples are noted during the daily refrigerator check, the Microbiologist or qualified lab personnel, gowned as per SOP 880, will remove the samples from the laboratory media refrigerator while still in the sealed storage bag. Qualified personnel are trained in the following SOPs: 700, 705, 715, 720, 800, 820, 850, 855, 856, 860, 880, 900 and 905. The refrigerator door will remain open no longer than three minutes. 2. Samples will be processed using the Milliflex Plus Pump as per SOP 735. 3. The samples will then be organized into the 30-35⁰C Incubator per SOP 905. Samples will be stacked together and not placed into racks. The incubator door will remain open no longer than three minutes during any single evolution. They will remain there for 7 or more days.

ATS-ATP-5856 Page: 4 of 5 4. Upon completion of this incubation period, samples will be removed and placed in the BSC to be analyzed for growth. 5. Document all movement and procedures on laboratory chain of custody forms and in appropriate logbooks. 5. Transfer in an aseptic manner to the second incubator at 20-25⁰C for 7 or more days. 6. Remove plates and place in the BSC for analysis and identification. All plates, regardless of growth, will be documented pictorially following SOP 725 and any growth will be analyzed following SOPs 920 and 925. 7. Complete laboratory chain of custody forms with colony counts and fill out all appropriate logbooks. 8. Samples which have completed analysis will be stored and refrigerated for two weeks after the issuance of the final report. They will then be disposed of in accordance with the SOP for the autoclave being used.

ATS-ATP-5856 Page: 5 of 5 9. Complete all appropriate paperwork. All completed paperwork will be reviewed by the Quality Manager. 10. Document all movement and procedures on laboratory chain of custody forms and in appropriate logbooks. 9. Equipment Power Failure 1. In the event of a power failure that results in the equipment (i.e. the laboratory media refrigerator or any incubator) drifting outside of operational parameters, an internal investigation will be performed, as per SOP 930.