Tuesday, June 06, 2006

BRIEF OUTLINE OF THE FACILITIES WE HAVE

1. Tablet , Capsule ,Liquid Orals Production Area
Separate production area for Tablet , Capsule & Liquid Orals. Facilities , advanced equipments are installed to conform with the WHO c GMP norms .The production area provides appropriate personnel and material flow.


2. Ware Housing- Separate Areas With Following Departments
(A) Receipt Bay
(B) Quarantine & Rejection area
(C) Raw material store for Beta and Non Beta lactum materials
(D) Dispensing area with dust control system
(E) Packing material store adjoining the label library
(F) Engineering and Miscellaneous items stores.
(G) Finished goods store with Recall room


3. Quality Assurance -Department Comprises Of
(A) Central Quality Control Laboratory with Instruments , Chemical In process
Quality Control ,Microbiological testing facility
(B) Documentation.
(C) Control samples and Stability.
(D) Validation Analysis
(E) Internal Quality Audits
(F) Culture disposal pit.


4. Documentation And Record System
Each Batch is processed under controlled series of In Process Checks which are recorded in the batch production records as per the Master formula Records . On completion of any batch the samples are checked by Quality Control Lab and released for finished goods transfer. All necessary details are recorded in batch production. The Batch is transferred to Finished Goods store for further distribution.


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