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.