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The quality management system is established with an understanding that "product qualities as well as performance quality "are crucial in the long term survival of the organization.
The quality management system stresses upon the following key aspects:
The products are produced so that they conform to the 'product specifications'. This is achieved through utilization of validation system for process and equipments.
 The operating systems are designed to have minimum variation on account of people, materials ,machines and equipments through trained qualified Personnel, procurement of raw/packing materials through critically selected vendors, standard operating procedures & standard test procedures. The apecification for all products are done as per prescribed pharmacopial norms and standards. Machines and equipments only there products are reached they are quality assurance department for distribution/sale that conforms to the specifications prescribed lay the concerned department.
Samples are accepted based an systematic plan that prescribe how to sample raw materials / finished products ,that plays a major role to bring the product up to the desired quality level. Thus 'a sampling plan' specifies the number of samples to be collected.
 Appreciation through performance appraisals and increment and other facilities are provided to personnel from time to time. Periodical programmes are undertaken to motivate personnel that improves quality and productivity such training programmes are also undertaken so as to ensure continuous improvement in skills, knowledge and other important ingredients.
'Quality audits are performed at regular intervals by a self inspection team comprising of representatives from "Quality Assurance'', Production, maintenance and personnel department, this ensures that the standard operating procedures ( SOPs) are being followed by all the trained staff accordingly and give suggestions on any modifications and revisions in the same . Other aspects like environmental monitoring, quality of product, sanitation are taken on priority.
- Separate β-lactum production Block.
- Tab. & caps. Production block.
- Ware housing separate blocks.
- Advance control with microbiological testing facilities & Quality assurance department.
- Engineering services.
- Ventilation and Air Handling system.
- Document & record system as per their respective standard operative procedures.
- Calibration & validation system procedures.
- Beautiful elevation with green and fragrance garden
Product list :
Following packs variations are available:
Tablet section - Blister, strip & bulk pack
Capsules section - Blister, strip & bulk pack
β-lactum Section - Blister, strip,Dry syrup & Bulk pack
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