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SOP of Handling of Rework Residues from Batch Process
Following stated defects can be considered for storage and addition as rework in a batch leftover granules, chipping / capping defects, lamination, tablets with variations in physical parameters like weight, hardness, thickness, friability or edge broken tablets at the time of compression, coating and inspection. Residue after compression, blister, encapsulation & PFS is also being considered as rework.
SOP
SOP of Procedure for Training in Pharmaceuticals
Employee training at the place of work while he or she is doing the actual job. It is a one-on-one training or in small group preferably of 5 to 7 located at the job site, where someone who knows how to do a task shows another how to perform it. On-the-job training takes place in a normal working situation, using the actual tools, equipment, documents or materials that trainees will use when fully trained.
SOP
SOP for Pharmaceuticals Water Handling System
This SOP is applicable for the Production Area of abc Pharmaceuticals Limited.
Three types of water used in Manufacturing area.
1. Potable Water
2. Hot Water
3. Purified Water
SOP
SOP for Good Documentation Practice
1. Purpose:
To define the common practice to be followed for data entry in all GMP / GLP records.
2. Scope:
This procedure is applicable to all GMP / GLP records filled manually at Pharmaceutical Limited. This SOP is a general guideline and will be superseded whenever any specific requirements are mentioned in other SOP or approved documents.
SOP