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
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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.
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Products that CompanyManufactures:
• Tablets: Artikon,Anantavati, Sildenafil, etc.
• Capsules: Glibofit, Florium, etc.
• Oral Liquids: Alteykaananta syrup, etc.
• Dry Powder Injection: Ceftriaxone, Cefepime, Ceftazidime, etc.
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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
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.
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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
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RESEARCH & DEVELOPMENTDEPARTMENT
● New product formulation
● Reformulation
● Reprocess
● Troubleshooting
● Preparation of BPR for a new product
● Development of existing product
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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.
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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
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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
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IN-PROCESS TEST FORCAPSULE
1. Physical appearance
2. Disintegration test
3. Average weight
4. Weight variation
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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.
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IN PROCESS QUALITYCONTROL TESTS
Leak Test
Clarity Test
Weight Variation
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RESPONSIBILITIES OF QUALITYCONTROL
IN PHARMACEUTICALINDUSTRY
The main responsibilities of quality control in pharmaceutical industry include:
A. Efficacy
B. Safety
C. Quality
D. Compliance
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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
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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
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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.
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