| 1.0 | OBJECTIVE : | ||||||
| To lay down a procedure for receiving and allotting column number for HPLC | |||||||
| and GC column. | |||||||
| 2.0 | RESPONSIBILITY : | ||||||
| 2.1 | Documentation officer shall store, issue and control the HPLC / GC columns. | ||||||
| 2.2 | Head AD / QC to ensure compliance. | ||||||
| 3.0 | PROCEDURE : | ||||||
| 3.1 | After receiving GRIR from store, the officer Analytical Development / Quality | ||||||
| Control shall check the HPLC or GC columns against the purchase requisition. | |||||||
| (specifications). | |||||||
| 3.2 | The Officer Quality Control / Analytical Development shall submit the GRIR | ||||||
| with comments to Head - Analytical Development / Quality Control. | |||||||
| 3.3 | The Head - Analytical Development / Quality Control or their designee shall | ||||||
| approve the GRIR and send it to stores with comments. | |||||||
| 3.4 | Officer - QC / AD shall raise the store indent for approved columns and submit | ||||||
| the HPLC / GC columns to Documentation Officer. | |||||||
| 3.5 | On the receipt of HPLC / GC columns the Documentation Officer shall enter the | ||||||
| details in the respective column stock card (Annexure-1) and column entry | |||||||
| format in Microsoft Excel sheets (Annexure-3) and allot the column reference | |||||||
| number and keep the HPLC / GC columns in appropriate storage area. The | |||||||
| Documentation Officer shall mention the column reference number on | |||||||
| Manufacturers certificate, column and column box (if any) and file the manufacturer | |||||||
| certificate in respective file. | |||||||
| 3.6 | Column reference number shall consists of 6 characters. | ||||||
| 3.6.1 | The first two characters denote LC for liquid chromatography or GC for gas | ||||||
| chromatography. | |||||||
| 3.6.2 | The third character 'C' denotes column. | ||||||
| 3.6.3 | The last three characters are serial numbers in sequential order, starting from 001 | ||||||
| for HPLC and GC columns separately. | |||||||
| Example : | |||||||
| The reference number for the first HPLC column received shall be numbered | |||||||
| as LCC001. | |||||||
| The reference number for the first GC column received shall be numbered | |||||||
| as GCC001. | |||||||
| 3.7 | If any new HPLC / GC columns required, Officer Analytical Development / | ||||||
| Quality Control shall raise "HPLC / GC columns request" and submit to Head - | |||||||
| Analytical Development / Quality Control (Refer Annexure - 2). | |||||||
| 3.8 | After approval, Documentation Officer will issue the new column to Officer - | ||||||
| Analytical Development / Quality Control and enter the issue details in respective | |||||||
| columns stock card (Annexure-1) and Microsoft Excel Sheet (Annexure-3). | |||||||
| 3.9 | While issuing the column, Officer-Documentation shall open "Column Usage Log" | ||||||
| (annexure -5) by entering the column details, i.e., column description, In-house | |||||||
| column ID No., Part No., and Lot No. | |||||||
| 3.10 | After receiving the column, Officer- AR&D/QC shall enter the details of Usage | ||||||
| whenever the column is used for analysis. | |||||||
| 3.11 | Once the column is expired Officer AR&D / QC shall raise the "HPLC / GC | ||||||
| expired column handover form" (Annexure-4) and submit to Head AR&D / QC | |||||||
| for approval along with the column and its filled usage log. | |||||||
| 3.12 | After approval Documentation Officer shall enter receipt details in Microsoft | ||||||
| Excel Sheet (Annexure-3). | |||||||
| 3.13 | Officer Documentation shall file the HPLC / GC column request and HPLC/GC | ||||||
| expired handover form in respective files. | |||||||
| 4.0 | DOCUMENTATION : | ||||||
| 4.1 | Specimen format of Columns Stock Card - Annexure 1. | ||||||
| 4.2 | Specimen format of Columns request - Annexure 2. | ||||||
| 4.3 | Specimen format of Columns control format - Annexure 3. | ||||||
| 4.4 | Specimen format of Expired Columns handover form - Annexure 4. | ||||||
| 4.5 | Specimen format of Column Usage log - Annexure 5. | ||||||