sop for in process controls during granulation compression coating inspection

  sop for in process controls during granulation compression coating inspection   1.0 OBJECTIVE:    The objective of this SOP is: 1.1 To describe the procedure for monitoring the Quality of Tablets during granulation, compression, coating, inspection operation. 2.0 RESPONSIBILITIES: 2.1 Quality Assurance Officer / Executive shall be: 2.1.1 Responsible for assuring the quality of … Read more

sop for non conformance of RM PM and finished product

  sop for non conformance of RM PM and finished product 1.0. OBJECTIVE:  The objective of this SOP is: 1.1 To describe a procedure for Handling of Non Conformance (NCR) of Raw Material (RM) / Packaging Material (PM) and Finished Product (FP). 1.1.1 Raw material / finished product which conforms to Regulatory specifications but does … Read more

sop for collection storage and disposal of control samples

  sop for collection storage and disposal of control samples   1.0 OBJECTIVE:  The objective of this SOP is: 1.1 To describe the procedure for collection, storage and disposal of control samples. 2.0 RESPONSIBILITIES: 2.1 Quality Assurance Officer shall be: 2.1.1 Responsible for collection of control sample of finished products. 2.1.2 Updation of Control Sample … Read more

sop for trend analysis of finished products

  sop for trend analysis of finished products     1.0. OBJECTIVE:  The objective of this SOP is: 1.1 To describe a procedure for Trend Analysis of finished products. 2.0. RESPONSIBILITY: 2.1 Head of the Quality Control shall be: 2.1.1. Responsible for preparing the trend analysis of finished products by considering the Analytical parameters. 2.2 … Read more

sop for numbering and approval of formats

  sop for numbering and approval of formats   1.0. OBJECTIVE:  The objective of this SOP is: 1.1 To describe procedure for approval and numbering of Formats. 2.0. RESPONSIBILITY: 2.1 Head of the respective Department shall be: 2.1.1. Responsible for preparing the format as per their requirement. 2.1.2. Responsible for taking approval of Quality Assurance. … Read more

Hetero pharma walk in drive

Hetero pharma walk in drive Hetero is offering a walk in drive for various post on 6 feb 2021. Full details of the job is given below. Description of the job  Vacant post – Production Education Required for the job – B.pharma , M.pharma Experience – 02 to 06 years  Salary – No cap for … Read more

sop for rework procedure

sop for rework procedure   1.0. OBJECTIVE:  The objective of this SOP is: 1.1 To describe a procedure for Rework of dosage forms which require change of packaging components(s). 2.0. RESPONSIBILITY: 2.1 Initiating Department shall be: 2.1.1 Responsible to fill up the requisition for rework in the form 2.1.2 Responsible seeking recommendations of Head – … Read more

sop for tolerance in the schedule of calibration

  sop for tolerance in the schedule of calibration   1.0. OBJECTIVE:  The objective of this SOP is: 1.1 To describe a procedure for acceptable tolerance limit for the frequency of calibration of instruments. 2.0. RESPONSIBILITY: 2.1 Officer of Concerned Department shall be: 2.1.1 Responsible for calibration of the instrument in co-ordination with the Engineering … Read more

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