A PROJECT
ON
INDUSTRIAL TRAINING REPORT
DEPARTMENT OF PHARMACY
Dr. Bhimrao Ambedkar University
Khandari, Agra- 282002
Session 2018-19
Under Guidance of
Mrs. POOJA SHARMA
(Assistant Professor)
Presented by:
KISHAN PATEL
Final Year( VIII Semester)
(Roll No. …………………..
INTRODUCTION
Pharmaceutical Industry
Swiss Garnier is a global pharmaceutical manufacturer specializing in
development and production of innovative pharmaceutical formulations.
Incorporated in 2006 as a contract manufacturing company, today the
company has a turnover of over 350 crores INR.
Swiss Garnier is committed to customer satisfaction, employee
empowerment and environmental care.
Swiss Garnier Bio Tech, 21,
Industrial Area, Mehatpur Distt.
Una (H.P)
FSSAI Licence No.: 10914012000061
Drug Lic. No. FORM 25 : NNZ/2016/109
FORM 28 : BNZ/2016/109
Webside: www.swissgarniarer.com
DEPARTMENTS OF INDUSTRY
 Warehouse
- Raw Material Store
- Quarantine Area
- Finish Good Store
 Production Department
 Quality Control Department
 Quality Assurance Department
 F&D Department
 Maintenance Department
 Marketing Department
Tablet Section
Tablets are unit solid dosage form of medicament or
medicaments with or without suitable diluents.
Steps involved in the Tablet Manufacturing:
 Dispensing of Raw Material
 Granulation
 Multi-mill (for size reduction)
 Sifting/Sieving
 Blending (to ensure a homogeneous mixture)
 Compression
Various Parameters for Tablets
 D.T (disintegration time)
 Friability
= Initial weight – final weight × 100
Initial weight
 Hardness
 Thickness
 Weight variation
Acc. To I.P. and B.P. :- 0-80mg±10%
<80-250±7.5%
<250±5%
QUALITY CONTROL
DEPARTMENT
Raw material inspection
↓
Raw Material
↓
Receipt
↓
Verification
↓
Sampling
↓
Under Test
↓
Q.C Testing
↓
Approved Rejected
↓ ↓
For manufacturing Return to supplier/ Distributer
Quality Assurance (Q.A.)
Role of Quality Assurance in industry:
 Temperature check
 Humidity checking
 Stability testing
 Maintain record
 Dispatch testing
 Handling of market complains
 Dispensing checking
 In-process testing
 SOP designing
 Workers training
 Validation
 Self-inspection/ internal audit
DISCUSSION
 Swiss Garnier Bio Tech Pharmaceutical enhanced understanding
of Academic knowledge and skills.
 It indeed polished my knowledge and experience confined only
to books and theoretical learning majorly.
 Application of these theories and lectures delivered in classrooms
differ a little from the specifically set format.
Not only pharmacists in production areas but even workers helped
me to understand important procedures regarding the production.
The entire journey of training allowed me to identify my strengths
and weaknesses, and use both of them to the best advantage of my
career.
Industrial training report

Industrial training report

  • 1.
    A PROJECT ON INDUSTRIAL TRAININGREPORT DEPARTMENT OF PHARMACY Dr. Bhimrao Ambedkar University Khandari, Agra- 282002 Session 2018-19 Under Guidance of Mrs. POOJA SHARMA (Assistant Professor) Presented by: KISHAN PATEL Final Year( VIII Semester) (Roll No. …………………..
  • 2.
    INTRODUCTION Pharmaceutical Industry Swiss Garnieris a global pharmaceutical manufacturer specializing in development and production of innovative pharmaceutical formulations. Incorporated in 2006 as a contract manufacturing company, today the company has a turnover of over 350 crores INR. Swiss Garnier is committed to customer satisfaction, employee empowerment and environmental care. Swiss Garnier Bio Tech, 21, Industrial Area, Mehatpur Distt. Una (H.P) FSSAI Licence No.: 10914012000061 Drug Lic. No. FORM 25 : NNZ/2016/109 FORM 28 : BNZ/2016/109 Webside: www.swissgarniarer.com
  • 3.
    DEPARTMENTS OF INDUSTRY Warehouse - Raw Material Store - Quarantine Area - Finish Good Store  Production Department  Quality Control Department  Quality Assurance Department  F&D Department  Maintenance Department  Marketing Department
  • 4.
    Tablet Section Tablets areunit solid dosage form of medicament or medicaments with or without suitable diluents. Steps involved in the Tablet Manufacturing:  Dispensing of Raw Material  Granulation  Multi-mill (for size reduction)  Sifting/Sieving  Blending (to ensure a homogeneous mixture)  Compression
  • 5.
    Various Parameters forTablets  D.T (disintegration time)  Friability = Initial weight – final weight × 100 Initial weight  Hardness  Thickness  Weight variation Acc. To I.P. and B.P. :- 0-80mg±10% <80-250±7.5% <250±5%
  • 6.
    QUALITY CONTROL DEPARTMENT Raw materialinspection ↓ Raw Material ↓ Receipt ↓ Verification ↓ Sampling ↓ Under Test ↓ Q.C Testing ↓ Approved Rejected ↓ ↓ For manufacturing Return to supplier/ Distributer
  • 7.
    Quality Assurance (Q.A.) Roleof Quality Assurance in industry:  Temperature check  Humidity checking  Stability testing  Maintain record  Dispatch testing  Handling of market complains  Dispensing checking  In-process testing  SOP designing  Workers training  Validation  Self-inspection/ internal audit
  • 8.
    DISCUSSION  Swiss GarnierBio Tech Pharmaceutical enhanced understanding of Academic knowledge and skills.  It indeed polished my knowledge and experience confined only to books and theoretical learning majorly.  Application of these theories and lectures delivered in classrooms differ a little from the specifically set format. Not only pharmacists in production areas but even workers helped me to understand important procedures regarding the production. The entire journey of training allowed me to identify my strengths and weaknesses, and use both of them to the best advantage of my career.