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APPLE FORMULATIONS PVT. LTD., AN ISO 9001:2008 & GMP CERTIFIED COMPANY (MANUFACTURER & EXPORTER)

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GENERAL DESCRIPTION OF ACTIVITIES

Manager ĘC Quality Control heads the quality control unit.
Quality control is responsible for physical, chemical and microbiological testing (wherever applicable) of starting materials, packaging materials, semi-finished (In-process/ bulk) products and finished products, environment, services and utilities.
Quality Control is also for carrying out the In-process Quality Control checks.


QUALITY CONTROL PROCEDURES:

To maintain & implement quality system in QC dept. Sampling & analyzing the raw materials, in-process/ bulk products, finished and packaging materials.
Calibration of inspection, measuring & test equipment & maintaining their records.
To maintain good laboratory practices.
Immediate investigation on customer complaints & queries.
Development of analytical methods for new raw materials & intermediates.
Checking of the calibration status of all the measuring & testing equipments.
Issuing/ checking test certificates for receipt, in process & final product stages.
Controlling & maintaining of all labels system.
Sending samples of finished products to customers.
To perform analytical validation & maintain records.


QUARANTINE AND RELEASE OF FINISHED PRODUCTS:

The finished goods are stored in work in progress areas.
The finished goods are sampled as per the approved sampling plans and they are tested using approved analytical methods against the approved release specifications.
The batch is released only by the authorized person after review of all analytical records, review of batch documentation, review of IPQC performance of the batch and review of production conditions, yield re-conciliation and final verification of conformance to the Product License requirements.