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Complete IPQC Tests for Pharmaceutical Tablet Dosage Form Coupon
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[25% Off] Complete IPQC Tests for Pharmaceutical Tablet Dosage Form Course Coupon

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Duration: 3.0 hours
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IPQC Tests for Pharmaceutical Tablet Dosage, Pharmacy Education, Weight, Hardness, Desintegration, Friability, Thickness

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Description

The development of a drug product is a lengthy process involving  drug discovery, laboratory testing, animal studies, clinical trials  and regulatory registration.

To further enhance the effectiveness  and safety of the drug product after approval, many regulatory  agencies such as the United States Food and Drug Administration  (FDA) also require that the drug product be tested for its identity,  strength, quality, purity and stability before it can be released for  use. For this reason, pharmaceutical validation and process controls  are important in spite of the problems that may been countered.

Process controls include raw materials inspection, in-process  controls and target so for final product. IPQC stands for in process  quality control. These are checks that are carried out before the  manufacturing process is completed. The function of of in-process  controls is monitoring and if necessary adaption of the  manufacturing process in order to comply with the specifications.

This may include control of equipment and environment too. In-process materials should be tested for identity, strength, quality and purity as appropriate and approved or rejected by the quality control unit during the production process.

Rejected  in-process materials should be identified and controlled under a quarantine system designed to prevent their use in manufacturing


DEFINITION OF IPQC

IPQC stands for IN PROCESS QUALITY CONTROL .

These are checks that are carried out before the manufacturing process is completed. The function of of in-process controls is monitoring and if necessary adaption of the manufacturing process in order to comply with the specifications .this may include control of equipment and environment too. In-process materials should be tested for identity, strength, quality and purity as appropriate and approved or rejected by the quality control unit during the production process. Rejected  in-process materials should be identified and controlled under a quarantine system designed to prevent their use in manufacturing .Written procedure should be established and followed that describe the in-process controls and tests as specified

QUALITY CONTROL EQUIPMENTS

  • Friabilator

  • Disintegration apparatus

  • Hardness Tester

  • Vernier Caliper

Course Eligibility :

Diploma Pharmacy Students

Bachelor of Pharmacy Students

Master of pharmacy Students

Pharmaceutical industry

Pharma Professionals


Benefits of course:

  1. Learning of IPQC Tests

  2. Tablet Dosage quality control

  3. Hadling of Equipments

  4. Theory & Practical demonstration

  5. Certificate of completion

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