JAI NARAIN VYAS UNIVERSITY, JODHPUR (RAJ.)
INDUSTRIALTRAINING REPORT
SUBMITTED TO: SUBMITTED BY:
MR. ASHWIN SINGH CHOUHAN LAKSHY RAWAL
ASSISTANT PROFESSOR B. PHARM. VII SEM (2024-25)
DEPARTMENT OF PHARMACOLOGY 22BPC22027
INTRODUCTION
• Ananta Medicare aims to protect and preserve the most important human
values - good health and quality of life.
• “Endless care about your health” is the main priority of Ananta Medicare.
• It manufacture all forms of drug delivery systems like, solid orals (tablets,
capsules, dry suspensions), liquid orals (syrups, suspensions), and injectable.
2
Products that Company Manufactures:
• Tablets: Artikon,Anantavati, Sildenafil, etc.
• Capsules: Glibofit, Florium, etc.
• Oral Liquids: Alteykaananta syrup, etc.
• Dry Powder Injection: Ceftriaxone, Cefepime, Ceftazidime, etc.
3
DEPARTMENTS
Admin Quality Control
Quality
Assurance
Production Warehouse
4
WORKING OF PRODUCTION UNIT
Dispensing
of raw
materials
De-
cartoning
Washing
Tunnel 5
Filling
Sealing
External
Vial
Washing
Visual
Inspection
Labelling
Packaging
6
TABLETS
● Pharmaceutical solid unit dosage form of medicament or medicaments with or
without suitable excipients and prepared either by molding or by compression.
● Active substances and excipients, usually in powder form.
● Pressed or compacted from a powder into a solid dose. 7
TABLETS MANUFACTURING PROCESS
Dispensing
Granulation
Compression
Coating
Packaging
8
CAPSULE
● Capsules are a solid dosage form in which the drug substance is enclosed in a
water-soluble shell or an envelope.
● Acapsule shell is made from gelatin.
9
LIQUID PREPARATION
Liquid preparations for oral use are usually solutions, emulsions or
suspensions containing one or more active ingredients in a suitable vehicle;
they may in some cases consist simply of a liquid active ingredient used as
such.
In liquid processing unit two types of liquid dosage form are manufactured. This
are :
● Syrup
● Suspension
10
RESEARCH & DEVELOPMENT DEPARTMENT
● New product formulation
● Reformulation
● Reprocess
● Troubleshooting
● Preparation of BPR for a new product
● Development of existing product
11
QUALITYASSURANCE (Q.A.)
● Quality assurance (Q.A.) is the sum total of organized arrangements made
with the object of ensuring that product will be of the quality required by
their intended use.
● Quality assurance is the systematic monitoring and evaluation of the various
aspects of a project, service or facility to maximize the probability that
minimum standards of quality are not being attained by the production
process.
● QA cannot absolutely guarantee the production of quality products.
12
ROLE OF QUALITYASSURANCE IN INDUSTRY
1. Temperature check
2. Humidity checking
3. In-process testing
4. SOP designing
5. Maintain record
6. Stability testing
7. Internal audit.
8. Handling of market complains
9. Market return
10. Dispensing checking
11. Line clearance
12. Validation
13. Dispatch testing
14. Self inspection
13
IN-PROCESS TEST FOR TABLETS
Q.C. perform following test for in-process testing of tablets
1. Appearance(color, size, shape)
2. Weight Variation
3. Disintegration
4. Hardness
5. Thickness
6. Dissolution time
7. Friability test
8. Average weight 14
IN-PROCESS TEST FOR CAPSULE
1. Physical appearance
2. Disintegration test
3. Average weight
4. Weight variation
15
QUALITY CONTROL DEPARTMENT
● QC is the part of GMP concerned with -
A. Sampling,
B. Specifications,
C. Testing
● Which ensure that the necessary and relevant tests are actually carried out.
● The materials are neither released for use nor products are used for sale &
supply until their quality has been satisfactory.
16
IN PROCESS QUALITY CONTROL TESTS
Leak Test
Clarity Test
Weight Variation
17
DOCUMENTATION
MFR
BMR
BPR
18
RESPONSIBILITIES OF QUALITY CONTROL
IN PHARMACEUTICALINDUSTRY
The main responsibilities of quality control in pharmaceutical industry include:
A. Efficacy
B. Safety
C. Quality
D. Compliance
19
INSTRUMENTS USED IN QUALITY CONTROL
AREA
● Karl Fischer titrator
● Polarimeter
● HPLC
● UV-visible spectrophotometer
● Tablet hardness & diameter tester
● IR spectrophotometer
● Dissolution tester
● Ph meter
● Disintegration tester
● Sonicator
● Magnetic stirrer
● Atomic absorption spectroscopy
● Analytical electronic balance
20
HPLC: HIGH PRESSURE LIQUID
CHROMATOGRAPHY
21
UV VISIBLE SPECTROSCOPY
22
MACHINES USED IN QC DEPARTMENT
23
WAREHOUSE DEPARTMENT
● Warehouse is the place where the bulk raw materials, packaging materials as
well as finished products are kept at their optimum storage condition.
● Raw materials and packaging material are tested as they enter the
warehouse and they transferred to the manufacturing department by
requisitions.
● The storage department of ANANTA Medicare limited includes the
following sections:
1. Raw materials store
2. Packing material store and
3. Finished product store
24
GENERALLY, THREE TYPES OF LABELS ARE
USED IN WAREHOUSE
25
CONCLUSION
● The pharmaceutical industry is the branch of the chemical industry that
develops, manufactures, and sells drugs.
● Defining illness is not its mission. Generally, the medications produced by
drug companies target diseases that have been defined previously by the
medical profession.
● It is also essential that these products are safe, effective, and of good quality,
and are prescribed and used rationally.
26
THANK YOU
27

Pharmaceutical Industrial Training report ppt

  • 1.
    JAI NARAIN VYASUNIVERSITY, JODHPUR (RAJ.) INDUSTRIALTRAINING REPORT SUBMITTED TO: SUBMITTED BY: MR. ASHWIN SINGH CHOUHAN LAKSHY RAWAL ASSISTANT PROFESSOR B. PHARM. VII SEM (2024-25) DEPARTMENT OF PHARMACOLOGY 22BPC22027
  • 2.
    INTRODUCTION • Ananta Medicareaims to protect and preserve the most important human values - good health and quality of life. • “Endless care about your health” is the main priority of Ananta Medicare. • It manufacture all forms of drug delivery systems like, solid orals (tablets, capsules, dry suspensions), liquid orals (syrups, suspensions), and injectable. 2
  • 3.
    Products that CompanyManufactures: • Tablets: Artikon,Anantavati, Sildenafil, etc. • Capsules: Glibofit, Florium, etc. • Oral Liquids: Alteykaananta syrup, etc. • Dry Powder Injection: Ceftriaxone, Cefepime, Ceftazidime, etc. 3
  • 4.
  • 5.
    WORKING OF PRODUCTIONUNIT Dispensing of raw materials De- cartoning Washing Tunnel 5
  • 6.
  • 7.
    TABLETS ● Pharmaceutical solidunit dosage form of medicament or medicaments with or without suitable excipients and prepared either by molding or by compression. ● Active substances and excipients, usually in powder form. ● Pressed or compacted from a powder into a solid dose. 7
  • 8.
  • 9.
    CAPSULE ● Capsules area solid dosage form in which the drug substance is enclosed in a water-soluble shell or an envelope. ● Acapsule shell is made from gelatin. 9
  • 10.
    LIQUID PREPARATION Liquid preparationsfor oral use are usually solutions, emulsions or suspensions containing one or more active ingredients in a suitable vehicle; they may in some cases consist simply of a liquid active ingredient used as such. In liquid processing unit two types of liquid dosage form are manufactured. This are : ● Syrup ● Suspension 10
  • 11.
    RESEARCH & DEVELOPMENTDEPARTMENT ● New product formulation ● Reformulation ● Reprocess ● Troubleshooting ● Preparation of BPR for a new product ● Development of existing product 11
  • 12.
    QUALITYASSURANCE (Q.A.) ● Qualityassurance (Q.A.) is the sum total of organized arrangements made with the object of ensuring that product will be of the quality required by their intended use. ● Quality assurance is the systematic monitoring and evaluation of the various aspects of a project, service or facility to maximize the probability that minimum standards of quality are not being attained by the production process. ● QA cannot absolutely guarantee the production of quality products. 12
  • 13.
    ROLE OF QUALITYASSURANCEIN INDUSTRY 1. Temperature check 2. Humidity checking 3. In-process testing 4. SOP designing 5. Maintain record 6. Stability testing 7. Internal audit. 8. Handling of market complains 9. Market return 10. Dispensing checking 11. Line clearance 12. Validation 13. Dispatch testing 14. Self inspection 13
  • 14.
    IN-PROCESS TEST FORTABLETS Q.C. perform following test for in-process testing of tablets 1. Appearance(color, size, shape) 2. Weight Variation 3. Disintegration 4. Hardness 5. Thickness 6. Dissolution time 7. Friability test 8. Average weight 14
  • 15.
    IN-PROCESS TEST FORCAPSULE 1. Physical appearance 2. Disintegration test 3. Average weight 4. Weight variation 15
  • 16.
    QUALITY CONTROL DEPARTMENT ●QC is the part of GMP concerned with - A. Sampling, B. Specifications, C. Testing ● Which ensure that the necessary and relevant tests are actually carried out. ● The materials are neither released for use nor products are used for sale & supply until their quality has been satisfactory. 16
  • 17.
    IN PROCESS QUALITYCONTROL TESTS Leak Test Clarity Test Weight Variation 17
  • 18.
  • 19.
    RESPONSIBILITIES OF QUALITYCONTROL IN PHARMACEUTICALINDUSTRY The main responsibilities of quality control in pharmaceutical industry include: A. Efficacy B. Safety C. Quality D. Compliance 19
  • 20.
    INSTRUMENTS USED INQUALITY CONTROL AREA ● Karl Fischer titrator ● Polarimeter ● HPLC ● UV-visible spectrophotometer ● Tablet hardness & diameter tester ● IR spectrophotometer ● Dissolution tester ● Ph meter ● Disintegration tester ● Sonicator ● Magnetic stirrer ● Atomic absorption spectroscopy ● Analytical electronic balance 20
  • 21.
    HPLC: HIGH PRESSURELIQUID CHROMATOGRAPHY 21
  • 22.
  • 23.
    MACHINES USED INQC DEPARTMENT 23
  • 24.
    WAREHOUSE DEPARTMENT ● Warehouseis the place where the bulk raw materials, packaging materials as well as finished products are kept at their optimum storage condition. ● Raw materials and packaging material are tested as they enter the warehouse and they transferred to the manufacturing department by requisitions. ● The storage department of ANANTA Medicare limited includes the following sections: 1. Raw materials store 2. Packing material store and 3. Finished product store 24
  • 25.
    GENERALLY, THREE TYPESOF LABELS ARE USED IN WAREHOUSE 25
  • 26.
    CONCLUSION ● The pharmaceuticalindustry is the branch of the chemical industry that develops, manufactures, and sells drugs. ● Defining illness is not its mission. Generally, the medications produced by drug companies target diseases that have been defined previously by the medical profession. ● It is also essential that these products are safe, effective, and of good quality, and are prescribed and used rationally. 26
  • 27.