Standard Operating Procedure for Technology Transfer in Gels Production
1) Purpose
The purpose of this SOP is to establish procedures for the systematic transfer of technology related to gels production from the development or existing site to another manufacturing site, ensuring consistency, quality, and compliance throughout the transfer process.
2) Scope
This SOP applies to all personnel involved in the pharmaceutical manufacturing facility’s technology transfer department, including Formulation Scientists, Production Engineers, Quality Assurance (QA), Regulatory Affairs, and Production personnel responsible for technology transfer activities.
3) Responsibilities
Formulation Scientists: Provide technical expertise and documentation related to the formulation and process.
Production Engineers: Implement equipment and process changes at the receiving site.
Quality Assurance (QA): Ensure compliance with SOPs and regulatory requirements throughout the transfer process.
Regulatory Affairs: Coordinate regulatory submissions and compliance activities associated with technology transfer.
Production Personnel: Execute procedures and protocols related to technology transfer at both sending and receiving sites.
4) Procedure
4.1 Planning and Preparation
4.1.1 Initiate technology transfer process by identifying sending and receiving sites, and establishing project timelines and milestones.
4.1.2 Formulate a Technology Transfer Plan outlining objectives, roles and responsibilities, and timelines for each phase of transfer.
4.2 Documentation and Knowledge Transfer
4.2.1 Compile comprehensive documentation including master batch records, manufacturing instructions, specifications, and validation protocols.
4.2.2 Conduct training sessions for personnel at the receiving site on procedures, equipment operation, and quality standards.
4.3 Trial Batches and Process Validation
4.3.1 Initiate trial batches at the receiving site to validate equipment, processes, and product quality.
4.3.2 Perform process validation studies according to approved protocols and regulatory requirements.
4.4 Performance Qualification and Regulatory Compliance
4.4.1 Execute performance qualification (PQ) studies to demonstrate that the production process at the receiving site consistently produces gel products meeting predefined specifications.
4.4.2 Ensure compliance with regulatory submissions, approvals, and notifications related to the technology transfer.
4.5 Continuous Monitoring and Optimization
4.5.1 Monitor production processes post-transfer to identify opportunities for optimization and improvement.
4.5.2 Implement corrective actions and continuous improvement initiatives as needed to enhance process efficiency and product quality.
4.6 Completion and Documentation
4.6.1 Complete technology transfer process by formalizing acceptance criteria and documentation of successful transfer.
4.6.2 Archive all transfer-related documents and maintain them in accordance with regulatory and company guidelines.
5) Abbreviations, if any
SOP: Standard Operating Procedure
PQ: Performance Qualification
6) Documents, if any
– Technology Transfer Plan
– Master Batch Records
– Manufacturing Instructions
– Validation Protocols and Reports
7) Reference, if any
– FDA Guidance for Industry: Technology Transfer Considerations for Pharmaceutical Products
– ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
– Company-specific technology transfer procedures and guidelines
8) SOP Version
Version 1.0
