Pharmaceutical Microbiology Manual
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ORA.007 Pharmaceutical Microbiology Manual
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O FFICE OF R EGULATORY A FFAIRS Office of Regulatory Science Document Number: ORA.007 Revision #: 02 Revised: 25 Aug 2020 Title: Pharmaceutical Microbiology Manual Page 63 of 92 For the most current and official copy, check QMiS. u. Soybean Casein Digest Broth (with neutralizers) v. Neutralizers (i.e. lecithin, tween, etc...) B. Sampling Preparation 1. Don appropriate personal protective equipment (PPE) as follows: Note: All ORS full gowning and procedures should be performed prior to conducting the collection. The firm’s procedures/guidelines should be adhered to when entering classified area; however, it is the expectation that the microbiologists entering the classified area, in order to perform sampling, will don sterile garments. If there is a dispute regarding the PPE to be donned for aseptic sampling, ORS Headquarters should be contacted prior to commencing gowning. a. Nonsterile Hair net and beard cover (if needed) b. Sterile mask c. Shoe covers (non-sterile) d. Sterile Gloves e. Sterile Disposable Coverall f. Sterile Hood g. Sterile Goggles h. Sterile Boot Covers 2. Sampling Equipment Controls a. Aseptic Technique Control: Place one (1) sterile Dacron or cotton swab into sterile water and place back into its sterile transport media solution. Place this negative control into a sterile Whirl- pak® bag. Note: This control may not be needed if the sponges and/or swabs are received pre-moistened. There is no surface contact for this control. b. Swab/Sponge Sterility Control: Place an intact unused swab (or sponge) unit into a sterile Whirl-pak® bag. c. RODAC/Hycheck Sterility Control: Place an unused RODAC plate and/or Hycheck plate within a sterile Whirl-pak® bag. d. Whirl-pak® bag Sterility Control: Include one unopened Whirl- pak® bag as a closed control. |
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