European Pharmaceutical Review

MARCH 11, 2024

Employing MALDI-TOF MS for microbial identification in sterile drug manufacturing Fungal contamination in pharmaceutical cleaning facilities Case study examples Mould and yeast have been reported by several previous authors in numerous pharmaceutical cleanrooms , cold rooms, and controlled areas, according to the authors.

Sterile Compounds 83

Sterile Compounds Compounding Packaging Pharmaceutical Companies 83

GMPSOP

OCTOBER 16, 2022

Table of Contents Contamination control is taken extremely seriously by the GMP facilities as it can adversely affect the quality and safety of food and drugs they produce. How to prevent cross-contamination in GMP facility? You must take numerous preventive measures to reduce or eliminate cross-contamination risks in GMP facility.

Health and Personal Care Stores 52

Health and Personal Care Stores Labelling Documentation Packaging 52

GMPSOP

MAY 17, 2024

GMP cleaning and sanitation practices in pharmaceuticals Pharmaceuticals quality assurance & validation procedures GMPSOP %title% Prev PREVIOUS POST GMP cleaning and sanitation of pharmaceutical equipment and facilities account for almost one-third of all production activities, if not more. It is impossible to sanitize a dirty surface.

Documentation 52

Documentation Packaging Pharmaceutical Manufacturing Compounding 52

GMPSOP

FEBRUARY 28, 2024

Basic cleaning and sanitation practices in Pharmaceuticals Pharmaceuticals quality assurance & validation procedures GMPSOP %title% Prev PREVIOUS POST Cleaning and sanitation of pharmaceutical equipment and facilities account for almost one-third of all production activities, if not more. It is impossible to sanitize a dirty surface.

Documentation 98

Documentation Packaging Pharmaceutical Manufacturing Compounding 98

pharmaphorum

JUNE 8, 2022

Cleanroom Managers. Implementation Strategy of Annex 1 in New or Existing Facilities. Led by: Richard Denk, Senior Consultant Aseptic Processing & Containment, Skan AG. Led by: Richard Denk, Senior Consultant Aseptic Processing & Containment, Skan AG. Leaders in Sterility Assurance. Regulatory Affairs Managers.

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GMPSOP

DECEMBER 28, 2022

These are also called cleanroom and controlled environments. The locations should provide good coverage of the whole cleanroom and associated areas such as – Changing rooms, – Air locks – Transfer hatches – Preparation areas etc. What are the cleanroom classifications and particulate limits? bioburden).

Documentation 52

Documentation Vaccines 52

GMPSOP

FEBRUARY 15, 2024

Good housekeeping practices in GMP Pharmaceuticals quality assurance & validation procedures GMPSOP %title% Prev PREVIOUS POST Good housekeeping practices include establishing cleaning procedures and schedules to ensure washrooms and toilet facilities are properly maintained. Accumulate rejected and imperfect goods in the designated area.

Documentation 52

Documentation Labelling Compounding Packaging 52