Revised SOPs for Ointments V 2.0

The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting Performance Qualification (PQ) of filling machines used in ointment manufacturing. This ensures that the machines consistently operate within specified parameters and meet quality and regulatory requirements.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting Operational Qualification (OQ) of mixing tanks in ointment manufacturing. This ensures that the mixing tanks operate consistently and reliably within specified parameters under normal operating conditions.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting Installation Qualification (IQ) of new, modified, or relocated equipment in ointment manufacturing. This ensures that all installed equipment complies with predefined specifications and regulatory requirements.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for equipment qualification in ointment manufacturing. This ensures that all equipment used in production meets predefined operational, performance, and compliance requirements before use.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for ensuring validation of all surfaces that come into contact with products, cleaning agents, and environmental conditions in ointment manufacturing. This ensures cleaning effectiveness, prevents cross-contamination, and maintains regulatory compliance.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for performing rinse sampling for cleaning validation in ointment manufacturing. This ensures that cleaning procedures effectively remove residues and comply with regulatory requirements.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for documentation of cleaning validation in ointment manufacturing. Proper documentation ensures compliance with regulatory requirements, traceability, and verification of cleaning effectiveness.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for conducting cross-contamination risk assessments in ointment manufacturing. This ensures that the risks of cross-contamination are identified, controlled, and mitigated to maintain product safety and regulatory compliance.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the process for reviewing cleaning validation data in ointment manufacturing. This ensures that cleaning procedures effectively remove residues, comply with regulatory standards, and maintain product safety.
Click to read the full article.

The purpose of this Standard Operating Procedure (SOP) is to define the validation process for cleaning detergents used in ointment manufacturing. This ensures that selected detergents effectively remove residues, do not introduce contaminants, and comply with regulatory requirements.
Click to read the full article.