SOPs for Elixers V 2.0

To define the environmental controls and conditions required during the dispensing of raw materials for elixir manufacturing to ensure product integrity, avoid contamination, and maintain regulatory compliance.
Click to read the full article.

To define the procedure for proper and compliant labeling of raw materials at the time of dispensing for elixir manufacturing. This ensures traceability, prevents mix-ups, and supports GMP documentation practices.
Click to read the full article.

To lay down the procedure for accurate and GMP-compliant dispensing of raw materials used in the manufacturing of elixirs to ensure correct quantities, avoid contamination, and maintain traceability.
Click to read the full article.

To describe the procedure for the controlled issuance of approved raw materials from the warehouse to the dispensing and manufacturing areas for the preparation of elixirs, ensuring traceability and compliance with GMP requirements.
Click to read the full article.

To define the procedure for proper storage of raw materials including APIs, excipients, and solvents used in elixir manufacturing to maintain their quality, identity, strength, and purity throughout the storage duration.
Click to read the full article.

To lay down a procedure for the sampling of raw materials received for the manufacturing of elixirs, ensuring that the samples represent the entire consignment and are suitable for quality evaluation before approval for use.
Click to read the full article.

To define the procedure for the receipt and initial verification of raw materials intended for elixir manufacturing, ensuring that all materials received meet the specified quality standards and regulatory requirements before they are accepted into the warehouse or production.
Click to read the full article.