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Assura Pharma Training Institute's Syllabus

Assura Pharma Training covers following points, and will updated time to time. Both Distance and Regular course covers following points.

  • Introduction

    • About us
    • Current scenario of pharmaceutical industry        
    • Types of pharmaceutical companies
    • Top 10 companies in India
    • Market of Pharmaceutical sector in India
  • Department's function & manufacturing process

    • Roll of all departments like HR, Purchase, Store, Production, QA, Regulatory and Safety.
    • Stages of tablet manufacturing like Dispensing, Blending, Granulation, Lubrication, Compression, Coating etc.
    • BMR & BPR preparation
    • Responsibilities of Production Department
    • Qualification & Validation of all equipments.
    • Guidelines for Pharma Packing Operations
    • Definitions used in pharmaceuticals
  • Quality Assurance

    • Established Manufacturing Control.
    • Audit compliance to the quality system..
    • Establish procedure and specification.
    • Ensure investigation of non-conformance
    • Quality cost analysis
    • Routine GMP audits
  • Quality Control

    • What is Quality Control ?
    • Functions of all sections like Raw material, packing material, finished product, stability, microbiology & Non-routine.
    • Maintaing of Good Laboratory Pracitces
    • Job Profile of QC personel's
    • Documentation
    • Safety
  • Non-complience, Softwares & Backup

    • Documentation for Non compliance like Incidents, OOS, OOT, Deviation, Change Control, etc.
    • (DQ, IQ, OQ, PQ) Qualification of instruments
    • Back up of various insturments
    • Various softwares used in instruments
  • Instrumentation, Calibration & Techniques

    • Weighing, sampling, dilutions, sample preparation, titrations used in QC.
    • Principle & functions of various instruments like HPLC, UV, IR, GC, pH Meter, KF Autotriator
    • Calibrations of all instruments
    • Maintaining of laboratory log book & e-records
    • Usage of working standards & their qualification
    • Pharmacopeia Standards.
  • F & D, Method Validation in R & D

    • Formulation Development
    • Terms used like Specificity, Linearity, Range, Accuracy Percision, Limit of Detection & Limit of Quantification.
    • Documentation in Laboratory Notebook.
    • Study to be conducted in R & D
  • Various Audits in pharma company

    • What is 21 CFR ?
    • Various pharma guidelines.
    • Requirements of audits like USFDA, MHRA, TGA, WHO, etc.
  • CV Preparation & Interview Skill Development

    • CV Preparation by experts
    • Interview preparation by skilled persons
    • Certification by "Assura Pharma Training Program".
    • Placement assistance provided by "ASSURA".
  • Performance Test

    • Every week Evaluation test
    • Prepartaion of Aptitude test
    • Final Performance test.