A REPORT SUBMITTED IN PARTIAL FULFILMENT

OF REQUIREMENT FOR THE DEGREE OF

BACHELOR OF PHARMACY
By:

SAURABH KUMAR (3rd Yr.)

(Roll No. - 2010390500074)
Under the Guidance of
Dr. Amit Chaudhary
(Principal)

RUDRA COLLEGE OF PHARMACY MAWANA KHURD, MEERUT

Submitted to the

Dr. APJ ABDUL KALAM TECHNICAL UNIVERSITY.

LUCKNOW
2023-2024
 DECLARATION

I Saurabh Kumar , hereby declare that work presented in the

industrial training report entitled in INDUSTRIAL TRAINING
P ERFORMED AT JANYA BIOCARE PVT. LTD. DIST-
HARIDWAR (U.K.) 247661
It si an authentic record of work carried out by
me during 01.02.2023 to 17.03.2023 at Janya Biocare
Pvt. Ltd. , under the guidance of DR. APJ Abdul Kalam
Technical University, Lucknow. Is being submitted for
partial fulfilment of the requirement for the award of bachelor
degree in B.Pharm. This is not been submitted anywhere else
for the award of any other degree/diploma.

Date-
P lace- Meerut.(UP)
Submitted By- Saurabh Kumar

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3
 ACKNOWLEGMENT

It is a matter of pleasure and happiness to make and submit

this industrial tra ining report during course of the completion
of this industrial work. Many of the persons have offered their
valuable and enormous support.
I’m thankful to all my teachers of Rudra College of
Pharmacy, Mawana Khurd Meerut For their blessings and
encouragement.
I would like to express my special thanks and gratitude to
JANYA BIOCARE PVT. LTD. and Mr. AVDESH KUMAR
Deore for providing all the essential facilities which were
required for this training.
Finally, I express my regards to my beloved parents who
inspired me throughout my studies and completion of this
training.

SAURABH KUMAR
Third Year B. Pharm
(Sem-6th)

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 INDEX

SR. NAME OF CONTENT

NO.
1 Introduction

2 Vision, Mission and Values

3 List of Products

4 Layout

5 Tablet and Orals Introduction

6 Details about Tablet and Oral

Liquids
7 Quality Control Section

8 Equipments

9 Conclusion

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 INTRODUCTION

Location- JANYA BIOCARE PVT. LTD.

KHASRA NO 169 TANSHIPUR
ROORKEE Dist.- HARIDWAR
Uttarkhand - 247661 India.

Site Capabilities-

Manufacturing Facility- Vitamins & Minerals Premixes

P rocessing, Primary Packing, Secondary P acking, and
Sachet filling machine
General Tablets Granulation Area, Three Compression
cubicles and three packing lines
State of art Quality laboratory-
Qualified and competent staff
Separate Wet and Instrument Lab
Class 100,000 Microbiology Setup
Labs are well equipped with latest infrastructure.
USFDA, WHO-GMP, ISO 9001, 14001,
22000,HACCP,SQF,Etc certifications.

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Salient Features-
Total Land Area- 35 Acres
Total construction area- 24,500m2
Four separate manufacturing facilities-

General Tablets
Oral liquids, Sugar coated Tablets, and Vitamins&
Minerals Premixes for Human Nutrition Health
Vitamins and minerals premixes for Animal
Nutrition Health
Herbal Plant

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 VISION, MISSION & VALUES

Vision-
Piramal Pharma Solutions are the leading healthcare
professionals with a top ranking position in (IND 12 th).
Piramal Pharma Solutions are leading manufacturer in
Vitamins and Minerals Premixes and Exporter of the
same.

Mission-
We Shall ensure the Quality, reliability, and innovation
thereby enhancing the sustainability and values for all
stakeholders.

Values-

Knowledge- Expertise and Innovation

Action- Entrepreneurship and Integrity
Care- Trusteeship and Humiluty
Impact- Performance and Resilience

The values that guide our culture are embodied in our

purpose-
“Doing Well and Doing Good ”

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 LIST OF PRODUCTS

1.Bactrim Syrup

2. Becozym C Forte

3. Paraxin Suspension

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4. Basiton C forte with Biotin Tablet

5. Bayers Tonic

6. Vitamin C Chewable

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7. Saridon Tablets

8. Benadon Tablets

9. Phosformin Tonic

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Layout

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Layout Of Orals Manufacturing Section

13
Layout Of Tablet Manufacturing
Section

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 Tablet and Oral Liquids

Tablets: Tablets is a pharmaceutical dosage form.

Tablets may be defined as the solid unit dosage form of
medicaments with or without diluents and prepared by
molding or compression. It comprises of active
substances and excipients. Usually in prepared powder
form, Pressed, or compacted from a powder into a solid
state. The excipients can include diluents, binders,
granulating , lubricating ,to ensure the efficient tableting.
Sweetners to give the flavor, disintegrants to promote the
break of tablet in stomach, and so on. The polymer
coating is done to make the tablet swallow easily.

The compressed tablet is most popular dosage form used

today. About two third of all prescriptions are dispensed
as solid dosage forms, and half of these are compressed
tablets. A tablet can be formulated to deliver an accurate
dosage to specific site. It is usually taken orally but can
be administered sublingually, buccally, rectally, or
intravaginally.

Advantages of Tablets:

1. Cost is lowest of all oral solid dosage forms

2. Lighter and compact.

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3. Easiest and cheapest to package and strip.
4. Sustained released product is possible by enteric
coating.
5. They are unit dosage forms and offer the greatest
capabilities of all oral dosage form for greatest dose
precision and the least content variability.
Disadvantages of Tablets:
1. Difficult to swallow in case of childrens and unconsious
patients.
2. Some drugs resist compression into dense compacts,
owing to amorphous nature, low density character .

Orals Liquids: Oral liquids are the homogeneous

liquid preparations, usually contains a solution, an
emulsion or a suspension or one or more active ingredients
in a suitable liquid base. They are prepared for oral
administration rather as such or after dilution. They may
contain other substances such as suitable dispersing,
solubilizing, wetting, emulsifying, stabilizing, and
antimicrobial substances for preservation.
They may also contain suitable sweetening agents,
flavoring agents and permitted colored agents. If sodium
saccharin or potassium saccharin is used for sweetening,
then its concentration in pediatric preparations should not
be more than 5 mg per kg of body weight

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Types of Oral Liquids:
1. Syrup
2. Oral Suspension
3. Oral Solution
4. Oral Drops
5. Oral Emulsion
6. Mixture
7. Linctus
8. Elixir

Advantages of Oral Liquids:

1. Immediate available for absorption.
2. Easy administration
3. Bitter drugs can be given by this route

Disadvantages of Oral Liquids:

1. Less stable compare to solid dosage forms.
2. They are bulky and difficult for store and transport.
3. Incompa tibility is more.

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 DETAILS OF TABLET AND ORAL
LIQUODS

Tablet Manufacturing:
Manufacturing of the tableting blend:

In the tablet pressing process, the main guideline is to ensure

that the appropriate amount of the active ingredient is in each
tablet. Hence all the ingredients should be mix well. If the
sufficiently homogeneous mixture of the components cannot
be obtained with simple blending processes, the ingredients
must be granulated prior to compression to assure an even
distribution of the active compound in the final tablet. Two
basic techniques are used to granulate the powders for
granulation into the ta blets. Wet granulation and Dry
granulation. Powders that can be mixed welled do not require
granulation and can be compressed into tablets through direct
compression.

1. Wet granulation

Introduction:

The most widely used process of agglomeration in a

pharmaceutical industry is wet granulation. Wet
granulation process simply involve the wet mass of the
powder blend with a granulating liquid. Wetting size and

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 drying are important steps in involved in the wet
granulation.

Process:

1. Mixing of the drugs and excipients.

2. Preparation of the binder solution
3. Mixing of the binder solution with powder solution to
form wet mass.
4. Drying of the moist granules.
5. Mixing of the screened granules with disintegrant,
lubricant and glidant.

The wet granulation technique has some

limitations.

2. Dry granulation:

Introduction:

In dry granulation process the powder mixture is

compressed without the use of solvent and heat. It is the
least desirable of all method of granulation. The two
basic procedures are to form compact of material by
compression and then mill to the c ompact to obtain a
granules. Two methods are used for dry granulation. The
most widely used method is slugging where the powder

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is recompressed and the resulting tablet or slug are
milled to yield the granules. The other method is to
precompress the powder with the powder with pressure
rolls using a machine such as Chilosonator.

Roller compaction:

The roller compaction of powder by means of pressure

roll can also be accompanied by machine called
Chilosonator. Unlike tablet machine the chilosonator
turns out a compacted mass in a steady continuous flow.
The powder is fed down between the powder into the
compaction zone like slugs. The aggregates are milled or
screened out for the production into granules.

Processing Steps:

1. Selection of raw materials

2. Weighing
3. Size Reduction
4. Mixing (Precompression or slugging)
5. Screening
6. Lubrication
7. Compression
This method has also some advantages and
disadvantages too.

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3. Direct compression:

This method is used when a group of ingredients can be

blended and placed in a tablet press to make tablet
without any of the ingredients having to be changed. This
is not very common because many tablets have active
pharmaceutical ingredients which will not allow for
direct compression due to their concentration or
excipients used in formulations are not conductive to
direct compression. Granulation is the process of
collecting particle s together by creating bonds between
them.
This method is utilize simple operation it requires mixed
all the ingredients then go for the direct compression
using compressor machine. This method used when the
small dose of drug is directly used with diluent.

Manufacturing of Tablet:

First the powder is filled into the die from above. The
mass of powder is determined by the position of the
lower punch in the die, the cross section area of the die,
and the powder density. At this stage adjustment to the
tablet weight are normally made by repositioning the
lower punch. After the die filling upper punch is lowered
into the die and the powder is uniaxially compressed to a
porosity of between 5 and 20%. The compression can
takes place in one or two stages and for commercial
production occurs very fast. Finally the upper punch is
pulled up and out of the die and the tablet is ejected from
the die by lifting the lower punch until its upper surface

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 is flush with the top face of the die. Ths process is
repeated for each ta blet.

Common problems encounter in during tablet

manufacturing operati on include:
Fluctuations in tablet weight, usually caused by uneven
powder flow into the die due to poor powder flow
properties.
Fluctuations in dosage of the active pharmaceutical
ingredient, caused by uneven distribution of the API in
the tableting blend.
Sticking, mottling ,orange pill effect ,capping,
lamination, etc., are the problems were encounter in the
tablet manufacturing.

Tablet Coating:
An application of coating material to the exterior of tablet
with the intension of conferring benefit and properties to the
dosage form over uncoated variety.

Objective:
To mask color, odor and taste of drug.
To provide physical and chemical protection to drug.
To control release of drug from the tablet.
To provide physical elegance.

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Types of Tablet Coating
Sugar coating
Film c oating
P ress coating.

The materials used for coating may largely comprise

sucrose, water soluble film coating polymers or
substances which are soluble in intestinal secretions
but not in those of the stomach. This types of coating
can be applied by the pan or fluid bed processe s. The
compression coating technique is suitable for sugar
and enteric coa tings but not for film. The tablet
coating contains use of polymer , coloring agent, etc.

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 Orals Liquids

Steps for manufacturing of oral liquids;

1. P lanning of Material Requirement

2. Liquid Preparation
3. Filling
4. Labeling
5. Packaging
6. Sales of Drug Products

The above mentioned steps are usually involved in the

manufacturing of the oral liquids formulations in
stepwise manner. Each step has its unique role in the
process of manufacturing of the pharmaceutical oral
liquid dosage form.
The most important step in the manufacturing is the
planning of material require ment it usually done by the
quality peoples. By the proper planning one can set the
benchmark for the manufacturing. Liquid preparation is
another step which is play important role. Here the 75%
of work is done of the manufacturing of oral liquid.
Then filling and labeling are also done with the help of
labor assign to the same purpose.
After labeling packing is done to ensures the products
used for the mankind. Lastly the most important phase of
the oral liquid manufacturing is get performed called
sales of the drug products.

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List of the equipments used in the manufacturing:

1. Mixing and storage tank

2. Portable mixer
3. Colloid mill
4. Filter press
5. Semi automatic bottle filling machine
6. Water still
7. Labeling Machine

Formulation of Oral Liquids:

1 .Drug and range of excipients includes

a) The vehicle: purified water and oil
2. Co-solvents: Propylene glycol and glycerine
3. Surfactants: To enhance the surface activity
4. P reservatives: Used against microbial contamination
5. Sweetening agents: Glucose, saccharin, aspartame
6. Buffering agents: To regulate the pH of formulation
7. Antioxidants: BHA and BHT

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Evaluation of Oral Liquids:
1. Uniformity of content
2. Uniformity of weight and volume
3. Test for bacterial endotoxin
4. Leaker test
5. P yrogen test
6. Clarity of solution.

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 Quality Control Section

It is the essay method in substance such as drugs, packing,

material , raw material, adjuvant , containers are checked
according to the monograph as per standards given to the
pharmacopoeia.
Following are the equipments used in QC section:
1. Magnetic stirrer
2. Electronic and simple balance
3. Capsule disintegration tester
4. Dissolution test apparatus
5. pH meter
6. Autoclave
7. UV and visible spectrophotometer
8. Leaker test apparatus

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1. Autoclave: Autoclave is a device used to sterilize the
equipment and supply by subjecting them to high
pressure saturated at 121 degree Celsius for around 10-15
minutes.

Autoclave

2. pH meter : A pH meter is an electronic device used for

the measuring the pH of liquid formulation. A typical pH
meter consist of a special measuring probe connected to
an electronic meter that measure the display the pH
reading.

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 pH Meter

3. Dissolution Test Apparatus: In this apparatus the

dissolution study of tablet is carried out . A single tablet
is taken and placed in wire mesh basket connected to
variable speed motor by means of a shaft this basket is
immersed in the dissolution medium contain in 100ml;
flask. The flask is maintained a t 37+ -0.5 degree Celsius
by means of constant temp bath. Motor is adjusted to
specified speed and samples of fluid are withdrawn at
regular time interval to determine the amount of drug in
the solution.

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 Dissolution Test Apparatus

4. UV-Visible Spectrophotometer: UV Visible

spectrophotometer is used in pharmaceutical industry due
to its various applications. It is one useful in detection of
impurities, Food industry, forensic science, qualitative
and quantitative analysis are carried out with the help of
the same.

UV-Visibl e Spectrophotometer
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 CONCLUSION
In the end I am glad to tell you that training in
P IRAMAL PHARMA SOLUTIONS MAHAD DIST-
RAIGAD was an excellent and fabulous experience. During
the training I actually learned about the Pharmaceutical
company and above its working the theoretical knowledge is
worth for getting a degree, and it is accessible in the book.
We can only imagine about the thing we read, but practical
life is always different and exce llent one. During My training
period, I had seen the various instruments and apparatus in
the industry. The highly sophisticated instruments that work
precisely must be operated with intense care for optimum
use. We could acquire a lot of information regarding the
latest instruments and their working procedures.
Similarly from practical point of view a
pharmaceutical company is very difficult. During the
training session I tried to my leve l best to gain practical
knowledge as much as I can. I improved my basic classified
doubts and also understood the importance of maintaining of
quality of produc ts at Pharmaceutical company.
I was successfully able to complete my short venture of
training. Lastly I hope that my training report fulfill t he
intended requirements.
- Regards
SAURABH KUMAR
Third Year B Pharm
(Sem-6th)

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Notes

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