FAQs

Frequently Asked Questions
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Annex 1 is a GMP document published by the European Commission and dedicated to the manufacturing of sterile product. All pharmaceutical companies that produce sterile products must comply with these regulations.

  • Section – 7.13.1
    Goggle & Face Mask
    Eye coverings & face should be worn to cover & enclose all facial skin.

  • Section – 7.13 & 7.16
    Sterile Glove
    Sterile 400mm/600 Gloves in Nitrile & Latex, double donnable, provide extra coverage of arm, no risk of gap between garment & gloves.
    Gloves compatible with alcohol & disinfectant comply with standard SOP.

  • Section – 7.11 & 7.13.1
    Disposable & Reusable Garment
    Aseptically folded to comply with aseptic donning. Reusable garment should be subjected to qualification testing.

  • Section – 7.14
    Cleanroom Socks
    Outdoor clothing (other than personal underwear) should not be brought into changing rooms leading directly to Grade B and C cleanrooms. Facility suits, covering the full length of the arms and the legs & socks covering the feet, should be worn before entry to change rooms for Grades B and C. Facility suits & socks should not present a risk of contamination to the gowning area or processes.

  • Section – 4.33 & 4.34
    Disinfectant
    Terminology of cleaning has been replaced with “cleaning and disinfection”. Disinfection studies should be validated.

  • Section – 8.43
    Biological Indicator
    Suppliers should be qualified and transportation & storage conditions should be controlled in order that BI quality is not compromised. The COA must be assessed for D-value & Z-value suitability.

Products manufactured by JUNE or Principle like MesaLabs (USA), Contec Inc. (USA), Isofield (Malaysia), Microbiologics (USA), AdvantaPure (USA), Eldon James (USA) etc. Comply to new regulatory standards & available locally.

You can download the Certificate of Analysis for June Enterprises products directly from the website. The CoA includes:

  • Microscopic, macroscopic, and phenotypic characteristics of each lot

  • Proof of traceability to the original Reference Culture

To access the certificate, follow the instructions provided on the Certificate of Analysis page.
If you have any questions regarding the results or data in the CoA, please contact the Technical Support Department.

The Statistical Analysis Certificate is also available for download through the Certificate of Analysis page. This certificate includes detailed quantitative data for each microorganism lot, such as:

  • Mean Assay Value

  • Standard Deviation

  • Coefficient of Variation

  • 95% and 99% Confidence Intervals

This document is specific to quantitative microorganism lots.
For any questions or clarification about the statistical results, please reach out to the Technical Support Department.

Always consult your local regulatory guidelines for the proper disposal of biohazardous materials. In most cases, it is acceptable to:

  • Place used or expired materials in a designated biohazard waste container

  • Arrange for disposal through a licensed biohazard waste management company

Following these steps helps ensure safe handling and compliance with environmental and safety regulations.

If you are unsure about local requirements, contact your facility’s biosafety officer or local health authority for guidance.