This document outlines the syllabus and regulations for a Bachelor of Pharmacy (B. Pharm) course over eight semesters. It details the duration, medium of instruction, attendance requirements, and coursework for each semester. The courses cover subjects like human anatomy, pharmaceutical analysis, pharmaceutics, chemistry, and communication skills. Evaluation includes continuous internal assessment, sessional exams, and end semester exams. Marks are awarded based on attendance, assignments, tests, and practical work. Students must obtain a minimum of 50% marks to pass each course, and letter grades are assigned to indicate student performance and conversion to percentages.
Best Career Options after 12th Science in Indiastudy tok
Best career options after 12th Science biology- MBBS, BDS,BHMS,BAMS,BMLT,BPT, B Pharm, B.Sc. nursing, Science Math - Engineering ,BArch, pilot, Defense, merchant navy
Competition Gurukul is the brain Child of IIT Delhi & NSIT Aluminums to help the Students for preparing the competitive exams in the innovation way by classroom coaching & online Mode.
www.competitiongurukul.in
Call: 9015596280, 9313565406
B.Pharmacy-Syllabus containg details of b pharmasandeep526001
as per syllabus of b.pharma .: Pharmaceutical jurisprudence extends to international regulations and trade agreements governing the global pharmaceutical industry. International organizations like the World Health Organization (WHO) and agreements such as the World Trade Organization’s Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) set standards and guidelines for pharmaceutical regulations, trade, and intellectual property protection.
THE ROLE OF PHARMACOGNOSY IN TRADITIONAL SYSTEM OF MEDICINEDrugs of natural origin continue to be important for the treatment of many diseases worldwide.
Pharmacognosy a long-established pharmaceutical science, has played a diverse role in the discovery characterisation production and standardisation of these drugs.
herbal drugs play an important role as allopathic system drugs and also drugs of the traditional system of medicine
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
Ayurvedic medicine Ayurveda for short is one of the world's oldest holistic whole-body healing systems.
It was developed more than 3000 years ago in India.
It's based on the belief that health and wellness depend on a delicate balance between the mind body and spirit.
Its main goal is to promote good health not fight disease But treatments may be geared toward specific health problems.
The different dosage forms available under Ayurveda system are followingLIQUID DOSAGE FORMS
SOLID DOSAGE FORMS.
SEMI- SOLID DOSAGE
Ayurveda believe every person is made of five basic elements found in the universe space, air, fire, water, and earth.
These combine in the human body to form three life forces or energies, called doshas.
They control how your body works.
They are Vata dosha (space and air)
Pitta dosha (fire and water)
Kapha dosha (water and earth).
Vata DoshaThose who practice Ayurveda believe this is the most powerful of all three doshas.
It controls very basic body functions like how cells divide.
It also controls your mind, breathing, blood flow, heart function and ability to get rid of waste through your intestines.
If vata dosha is your main life force, you're thought to be more likely to develop conditions like anxiety, asthma, heart disease, skin problems, and rheumatoid arthritis.
Pitta DoshaThis energy controls your digestion, metabolism (how well you break down foods), and certain hormones that are linked to your appetite.
Things that can disrupt it are eating sour or spicy foods and spending too much time in the sun.
If it's your main life force, you're thought to be more likely to have disease, heart disease, high blood pressure, and infections.
Kapha DoshaThis life force controls muscle growth, body strength and stability, weight, and your immune system.
You can disrupt it by sleeping during the day, eating too many sweet foods, and eating or drinking things that contain too much salt or water.
If it's your main life energy, practitioners believe you may develop asthma and other breathing disorders, cancer, diabetes, nausea after eating, and obesity.
Ayurvedic TreatmentAn Ayurvedic practitioner will create a treatment plan specifically designed for you.
He'll take
FLAVONOIDSFLAVONOIDSClass of plant secondary metabolites
Word Flavonoids derived from the Latin word Flavus= yellow
Group of polyphenolic compounds which are found in fruits, flowers, seeds & vegetable
Structure of flavonoids The flavonoids are possessing 15 carbon atoms and two benzene rings joined by a linear three-carbon chain the skeleton can be represented as the C6 - C3 - C6 system.
The three-carbon (-C3-) may be included through an oxygen bond between the two phenyl rings into
1- A five-membered heterocyclic ring (furan) as in aurones.
2- A six-membered heterocyclic ring (pyran) to give flavonoids which constitute the largest group. The flavonoid aglycone consists of a benzene ring (A) condensed with a six-membered ring (C) pyran ring, which at 2nd position adds a phenyl ring (B) as a substituent. C6-C3-C6 structure.
Crystalline solids sharp MP.
Solubility in H2O & alcohol (Flavonoid glycoside)
Non-glycosidic flavonoid: Aglycon part-sol in organic solvents
3. Color: Flavonones Flavanol Isoflavones- Colorless
Flavonols Flavones Yellow Chalchones aurones Orange
Anthocyanidine acid Red
In basic: Blue
4. Flavanols: optically active
15 C skeleton 2 benzene linked by heterocyclic pyran ring
Being phenolic dissolves in alkalies → Yellow sol +HCl → colorless
Glycosidic linkage located at 3 or 7 C
Flavanones, Flaonoes are unstable compounds on oxidation → Chalcones, leucocyanidines
Flavonoid + FeCl3→ green/ purple/ red-brown color
CLASSIFICATION OF FLAVONOIDSDepending on the carbon of the C ring on which the B ring is attached and the degree of unsaturation and oxidation of the C ring.
B ring is linked in position 3 of the ring C are called isoavones
B ring is linked in position 4, neoavonoids.
The B ring is linked in position 2 and further subdivided on the basis of the structural features of the C ring.
These subgroups are avones, avonols, avanones, avanonols, avanols or catechins and anthocyanins.
Finally avonoids with open C rings are called chalcones.
Flavones (2-phenylchromen-4-one)
Have a double bond between positions 2 and 3 and a ketone in position 4 of the C ring. ex:- Apigenin, Luteolin
2. Flavonols (3-hydroxy-2-phenylchromen-4-one)
Have a hydroxyl group in position 3 of the C ring, which may also be glycosylated. Ex: Kaempferol, Rutin, Myricetin, Quercetin.
. Flavanones/ dihydroavones (2,3-dihydro-2-phenylchromen-4- one
Have C ring saturated; the double bond between positions 2 and 3 is saturated, ex: Hesperetin, Hespereidin, Naringenin
Subclassified: furanoavanones, prenylated avanones, pyranoavanones or benzylated avanones
4. Flavanonols (dihydroavonols)/ 3-hydroxy-2,3-dihydro-2-phenyl chromen-4-one
Are 3-hydroxy derivatives of avanones; ex:Taxifolin, Silymarin
1. Shinoda test to dry powder or extract add 5 ml95% ethanol few drops of conc HCI and 0.5 g magnesium turnings Pink colour observed.
2. To a small quantity of residue add lead acetate solution. The yellow-coloured precipitate is formed. The addition of an
Best Career Options after 12th Science in Indiastudy tok
Best career options after 12th Science biology- MBBS, BDS,BHMS,BAMS,BMLT,BPT, B Pharm, B.Sc. nursing, Science Math - Engineering ,BArch, pilot, Defense, merchant navy
Competition Gurukul is the brain Child of IIT Delhi & NSIT Aluminums to help the Students for preparing the competitive exams in the innovation way by classroom coaching & online Mode.
www.competitiongurukul.in
Call: 9015596280, 9313565406
B.Pharmacy-Syllabus containg details of b pharmasandeep526001
as per syllabus of b.pharma .: Pharmaceutical jurisprudence extends to international regulations and trade agreements governing the global pharmaceutical industry. International organizations like the World Health Organization (WHO) and agreements such as the World Trade Organization’s Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS) set standards and guidelines for pharmaceutical regulations, trade, and intellectual property protection.
THE ROLE OF PHARMACOGNOSY IN TRADITIONAL SYSTEM OF MEDICINEDrugs of natural origin continue to be important for the treatment of many diseases worldwide.
Pharmacognosy a long-established pharmaceutical science, has played a diverse role in the discovery characterisation production and standardisation of these drugs.
herbal drugs play an important role as allopathic system drugs and also drugs of the traditional system of medicine
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
AYURVEDA- INDIAN SYSTEM OF MEDICINE
CHINESE MEDICINE
UNANI SYSTEM OF MEDICINE
SIDDHA SYSTEM OF MEDICINE
HOMEOPATHY
Ayurvedic medicine Ayurveda for short is one of the world's oldest holistic whole-body healing systems.
It was developed more than 3000 years ago in India.
It's based on the belief that health and wellness depend on a delicate balance between the mind body and spirit.
Its main goal is to promote good health not fight disease But treatments may be geared toward specific health problems.
The different dosage forms available under Ayurveda system are followingLIQUID DOSAGE FORMS
SOLID DOSAGE FORMS.
SEMI- SOLID DOSAGE
Ayurveda believe every person is made of five basic elements found in the universe space, air, fire, water, and earth.
These combine in the human body to form three life forces or energies, called doshas.
They control how your body works.
They are Vata dosha (space and air)
Pitta dosha (fire and water)
Kapha dosha (water and earth).
Vata DoshaThose who practice Ayurveda believe this is the most powerful of all three doshas.
It controls very basic body functions like how cells divide.
It also controls your mind, breathing, blood flow, heart function and ability to get rid of waste through your intestines.
If vata dosha is your main life force, you're thought to be more likely to develop conditions like anxiety, asthma, heart disease, skin problems, and rheumatoid arthritis.
Pitta DoshaThis energy controls your digestion, metabolism (how well you break down foods), and certain hormones that are linked to your appetite.
Things that can disrupt it are eating sour or spicy foods and spending too much time in the sun.
If it's your main life force, you're thought to be more likely to have disease, heart disease, high blood pressure, and infections.
Kapha DoshaThis life force controls muscle growth, body strength and stability, weight, and your immune system.
You can disrupt it by sleeping during the day, eating too many sweet foods, and eating or drinking things that contain too much salt or water.
If it's your main life energy, practitioners believe you may develop asthma and other breathing disorders, cancer, diabetes, nausea after eating, and obesity.
Ayurvedic TreatmentAn Ayurvedic practitioner will create a treatment plan specifically designed for you.
He'll take
FLAVONOIDSFLAVONOIDSClass of plant secondary metabolites
Word Flavonoids derived from the Latin word Flavus= yellow
Group of polyphenolic compounds which are found in fruits, flowers, seeds & vegetable
Structure of flavonoids The flavonoids are possessing 15 carbon atoms and two benzene rings joined by a linear three-carbon chain the skeleton can be represented as the C6 - C3 - C6 system.
The three-carbon (-C3-) may be included through an oxygen bond between the two phenyl rings into
1- A five-membered heterocyclic ring (furan) as in aurones.
2- A six-membered heterocyclic ring (pyran) to give flavonoids which constitute the largest group. The flavonoid aglycone consists of a benzene ring (A) condensed with a six-membered ring (C) pyran ring, which at 2nd position adds a phenyl ring (B) as a substituent. C6-C3-C6 structure.
Crystalline solids sharp MP.
Solubility in H2O & alcohol (Flavonoid glycoside)
Non-glycosidic flavonoid: Aglycon part-sol in organic solvents
3. Color: Flavonones Flavanol Isoflavones- Colorless
Flavonols Flavones Yellow Chalchones aurones Orange
Anthocyanidine acid Red
In basic: Blue
4. Flavanols: optically active
15 C skeleton 2 benzene linked by heterocyclic pyran ring
Being phenolic dissolves in alkalies → Yellow sol +HCl → colorless
Glycosidic linkage located at 3 or 7 C
Flavanones, Flaonoes are unstable compounds on oxidation → Chalcones, leucocyanidines
Flavonoid + FeCl3→ green/ purple/ red-brown color
CLASSIFICATION OF FLAVONOIDSDepending on the carbon of the C ring on which the B ring is attached and the degree of unsaturation and oxidation of the C ring.
B ring is linked in position 3 of the ring C are called isoavones
B ring is linked in position 4, neoavonoids.
The B ring is linked in position 2 and further subdivided on the basis of the structural features of the C ring.
These subgroups are avones, avonols, avanones, avanonols, avanols or catechins and anthocyanins.
Finally avonoids with open C rings are called chalcones.
Flavones (2-phenylchromen-4-one)
Have a double bond between positions 2 and 3 and a ketone in position 4 of the C ring. ex:- Apigenin, Luteolin
2. Flavonols (3-hydroxy-2-phenylchromen-4-one)
Have a hydroxyl group in position 3 of the C ring, which may also be glycosylated. Ex: Kaempferol, Rutin, Myricetin, Quercetin.
. Flavanones/ dihydroavones (2,3-dihydro-2-phenylchromen-4- one
Have C ring saturated; the double bond between positions 2 and 3 is saturated, ex: Hesperetin, Hespereidin, Naringenin
Subclassified: furanoavanones, prenylated avanones, pyranoavanones or benzylated avanones
4. Flavanonols (dihydroavonols)/ 3-hydroxy-2,3-dihydro-2-phenyl chromen-4-one
Are 3-hydroxy derivatives of avanones; ex:Taxifolin, Silymarin
1. Shinoda test to dry powder or extract add 5 ml95% ethanol few drops of conc HCI and 0.5 g magnesium turnings Pink colour observed.
2. To a small quantity of residue add lead acetate solution. The yellow-coloured precipitate is formed. The addition of an
Volatile Oils
The odorous volatile principles of plant and animal sources are known as volatile oils.
They evaporate when exposed to air at ordinary room temperature so also called as ethereal oils.
They represent the essence or active constituents of plant so called as essential oils.
Properties
1. Soluble in alcohol, ether, and lipid solvents and insoluble in water.
2. Generally lighter than water.
3. They have characteristic odour and high refractive index
4. Optically active compounds.
5. They are secreted in special structures such as ducts, cells, trichomes and Lysigenous glands.
6. Commonly found in dicot plant families such as Umbelliferae, Labiatae, Zingiberaceae etc and present in entire plant or any part of plant.
Types of volatile oils- On the basis of chemical nature
1. Aldehyde volatile oil- Cinnamon, Lemon peel
2. Alcohol V. O.- Cardamom, Coriander
3. Ester VO- Mustard
4. Hydrocarbon VO- Turpentine
5. Ketone VO- Camphor, Musk
6. Phenolic VO- Clove
Chemical tests.A thin section of drug treated with alcoholic solution of Sudan-III- gives red colour.
2. A thin section of drug treated with a drop of tincture alkane- gives red colour.
Introduction: Number of medicinal plants containing organic constituents in conjugation with a sugar moiety
It can be l or 2 such compounds are called as glycosides.
They exert therapeutically significant effects on humans and animals Traditionally used in modern medicine because of their cardiotonic, purgative, analgesic, anti-arrhythmic, and demulcent action.
Definition:-Glycosides are defined as organic compounds from plants and animal sources which on enzymatic hydrolysis give one or more sugar moieties along with a non-sugar moiety.
Sugar moiety is called glycon and non-sugar moiety is called a-glycon.
Classification Of GLYCOSIDES
BASED ON THE CHEMICAL NATURE OF NON-SUGAR MOIETY
BASED ON THE NATURE OF SUGAR MOIETY
BASED ON LINKAGE BETWEEN GLYCON AND AGLYCON PORTION.
BASED ON THE THERAPEUTIC NATURE OF GLYCOSIDE
BASED ON THE CHEMICAL NATURE OF NON SUGAR MOIETY
a) Anthraquinone glycoside anthraquinone moiety as aglycon. Ex: senna
b) Sterol or cardiac glycoside: aglycon portion is a steroid molecule. Ex: digitalis molecule
e) Saponine glycoside
e) Isothiocynate glycoside Ex: black mustard.
d) Cyanogentic glycoside Ex: white cherry bark
f) Flavonoid glycoside Ex: Ruta graveolens, citrus bio
g) Coumarin glycoside or Furano coumarine glycoside:- Ex: celery fruit cost
h) Aldehyde glycoside Ex: vanilla pods
i) Phenol glycoside Ex salcive
J) Steroidal glycoside
k) Glucosidal bitter or miscellaneous glycoside Ex salix species
Glucoside: sugar portion is glucose
Rhamnoside: sugar portion is rhamnose
Pentoside sugar portion is pentose
Fructoside sugar portion is fructose
Arabinoside sugar portion is arabinose
O-glycosides: Sugar molecule is combined with phenol or –OH group of aglycon, for example, higher plants: senna, rhubarb, Amygdaline, Salicin, cardiac glycosides, anthraquinone glycosides like sennosides etc.
Glycone –O H+HO − aglycone → Glycone −O− Aglycone + H2O
2. N-glycosides: Sugar molecule is combined with N of the –NH (amino group) of aglycon, for example, nucleosides
Glycone –OH+H N − aglycone → Glycone− N − Aglycone + H2O
3. S-glycosides: Sugar molecule is combined with the S or SH (thiol group) of aglycon, Isothiocyanate glycosides: for example, Sinigrin from black mustard
Glycone –OH+H S − aglycone → Glycone− S − Aglycone + H2O
4. C-glycosides: Sugar molecule is directly attached to the C—atom of aglycon, for example, Anthraquinone glycosides like Aloin, Barbaloin, Cascaroside and Flavone glycosides, etc. Cochineal colouring matter- carminic acid
Glycone –OH+H C − aglycone → Glycone− C − Aglycone + H2O
Chemical Tests for Anthraquinone Glycosides.
a) Borntrager’s test.
b) Modified Borntrager’s test.
Chemical Tests for Saponin Glycosides
a) Haemolysis test.
b) Foam test
Chemical Tests for Steroid & Triterpenoid Glycoside .
a) Liebermann Burchard test
b) Salkowaski test
c) Antimony trichloride test
d) Zimmermann test
Chemical Tests For Cardiac Glycoside
a) Keller-kiliani test
b) Legal test
c) Baljet test
ALKALOIDS
Alkaloids are a class of naturally occurring organic compounds that mostly contain basic nitrogen atoms.
This group also includes some related compounds with neutral and even weakly acidic properties.
Alkaloids are derived from plant sources they are basic they contain one or more nitrogen atoms (usually in a heterocyclic ring) and they usually have a marked physiological action.
Function of alkaloids
they may function as stimulants or regulators in activities like growth, metabolism and reproduction.
They may act as reservoirs for protein synthesis
Properties of alkaloids
Alkaloids are colourless, crystalline, non-volatile, solids, a few such as coniine and nicotine are liquids and a few even coloured, viz. berberine is yellow.
the alkaloids are bitter in taste and have pronounced physiological activity
Classification of alkaloids
a. Taxonomic classification- On the basis of taxonomic profile of the drug. For ex. Solanaceous alkaloids.
b. Biogenetic classification- On the basis of amino acid precursor. For ex. Phenylalanine, Tyrosine alkaloids
c. Pharmacological classification- On the basis therapeutic activity of the alkaloid For ex. Morphine as analgesic, Quinine as antimalarial.
d. Chemical classification- On the basis of basic chemical structure of alkaloid. It is of further three types-
1. True alkaloid- The alkaloids which have all basic properties of alkaloids, derived from amino acid and contain Nitrogen in heterocyclic ring. Ex. Atropine, Morphine.
2. Proto alkaloid- The alkaloid in which nitrogen atom is not present in the ring, but it is present outside the ring I form of amino group, so also called amino alkaloids or biological amines. Ex. Ephedrine.
3. Pseudo alkaloids- Actually these are not alkaloids. These are not derived from amino acid and not give basic identification tests of alkaloids. These are Steroidal (Solanine), Terpenoidal (Diterpene alkaloid) and Purine alkaloid (Caffeine).
chemical classification of alkaloids
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Instructions for Submissions thorugh G- Classroom.pptxJheel Barad
This presentation provides a briefing on how to upload submissions and documents in Google Classroom. It was prepared as part of an orientation for new Sainik School in-service teacher trainees. As a training officer, my goal is to ensure that you are comfortable and proficient with this essential tool for managing assignments and fostering student engagement.
Model Attribute Check Company Auto PropertyCeline George
In Odoo, the multi-company feature allows you to manage multiple companies within a single Odoo database instance. Each company can have its own configurations while still sharing common resources such as products, customers, and suppliers.
Students, digital devices and success - Andreas Schleicher - 27 May 2024..pptxEduSkills OECD
Andreas Schleicher presents at the OECD webinar ‘Digital devices in schools: detrimental distraction or secret to success?’ on 27 May 2024. The presentation was based on findings from PISA 2022 results and the webinar helped launch the PISA in Focus ‘Managing screen time: How to protect and equip students against distraction’ https://www.oecd-ilibrary.org/education/managing-screen-time_7c225af4-en and the OECD Education Policy Perspective ‘Students, digital devices and success’ can be found here - https://oe.cd/il/5yV
We all have good and bad thoughts from time to time and situation to situation. We are bombarded daily with spiraling thoughts(both negative and positive) creating all-consuming feel , making us difficult to manage with associated suffering. Good thoughts are like our Mob Signal (Positive thought) amidst noise(negative thought) in the atmosphere. Negative thoughts like noise outweigh positive thoughts. These thoughts often create unwanted confusion, trouble, stress and frustration in our mind as well as chaos in our physical world. Negative thoughts are also known as “distorted thinking”.
1. Introduction B- Pharm course
• Mr Nandakishor B Deshmukh.
Assistant Professor
Department Of Pharmaceutics
Shraddha Institute Of Pharmacy, Kondala Zambre,
Washim.
1
29-06-2023
2. Pharmacy Council of India New Delhi
Rules
• Syllabus for the Bachelor of Pharmacy (B. Pharm) Course.
• [Framed under Regulation 6, 7 & 8 of the Bachelor of
Pharmacy (B. Pharm) course regulations 2014
2
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3. CHAPTER- I: REGULATIONS .
Duration of the program : The course of study for B.Pharm shall
extend over a period of eight semesters (four academic years) and
six semesters (three academic years) for lateral entry students.
Medium of instruction and examinations: Medium of
instruction and examination shall be in English.
Attendance And Progress : A candidate is required to put in at
least 80% attendance in individual courses considering theory and
practical separately.
Academic work: A regular record of attendance both in Theory
and Practical shall be maintained by the teaching staff of
respective courses.
3
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4. Table-I: Course of study for semester I
Course code Name of the course No. of
hours
Tuto
rial
Credit
points
BP101T Human Anatomy and Physiology I–Theory 3 1 4
BP102T Pharmaceutical Analysis I – Theory 3 1 4
BP103T Pharmaceutics I – Theory 3 1 4
BP104T Pharmaceutical Inorganic Chemistry –
Theory
3 1 4
BP105T Communication skills – Theory * 2 - 2
BP106RBT
BP106RMT
Remedial Biology/
Remedial Mathematics – Theory*
2 - 2
BP107P Human Anatomy and Physiology –
Practical
4 - 2
BP108P Pharmaceutical Analysis I – Practical 4 - 2
BP109P Pharmaceutics I – Practical 4 - 2
BP110P Pharmaceutical Inorganic Chemistry –
Practical
4 - 2
BP111P Communication skills – Practical* 2 - 1
BP112RBP Remedial Biology – Practical* 2 - 1
Total 32/34$/36# 4 27/29$/30#
4
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5. #Applicable ONLY for the students who have studied
Mathematics / Physics / Chemistry at HSC and appearing
for Remedial Biology (RB)course.
$Applicable ONLY for the students who have studied
Physics / Chemistry / Botany / Zoology at HSC and
appearing for Remedial Mathematics (RM)course.
* Non University Examination (NUE)
5
29-06-2023
6. Table-II: Course of study for semester II
Course
Code
Name of the course No. of
hours
Tutorial Credit
points
BP201T Human Anatomy and Physiology II – Theory 3 1 4
BP202T Pharmaceutical Organic Chemistry I – Theory 3 1 4
BP203T Biochemistry – Theory 3 1 4
BP204T Pathophysiology – Theory 3 1 4
BP205T Computer Applications in Pharmacy – Theory * 3 - 3
BP206T Environmental sciences – Theory * 3 - 3
BP207P Human Anatomy and Physiology II –Practical 4 - 2
BP208P Pharmaceutical Organic Chemistry I– Practical 4 - 2
BP209P Biochemistry – Practical 4 - 2
BP210P Computer Applications in Pharmacy – Practical* 2 - 1
Total 32 4 29
6
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7. Tables-III: Schemes for internal assessments and end semester examinations semester wise
Course code
Name of the course
Internal Assessment End Semester Exams Total
Marks
ContinuousMode SessionalExams Total Marks Duration
Marks Duration
BP101T Human Anatomy andPhysiology
I– Theory
10 15 1 Hr 25 75 3 Hrs 100
BP102T Pharmaceutical Analysis I –
Theory
10 15 1 Hr 25 75 3 Hrs 100
BP103T Pharmaceutics I – Theory 10 15 1 Hr 25 75 3 Hrs 100
BP104T Pharmaceutical InorganicChemistry –
Theory
10 15 1 Hr 25 75 3 Hrs 100
BP105T Communication skills –
Theory *
5 10 1 Hr 15 35 1.5 Hrs 50
BP106RBT
BP106RMT
Remedial Biology/ Mathematics – Theory* 5 10 1 Hr 15 35 1.5 Hrs 50
BP107P Human Anatomy and Physiology– Practical 5 10 4 Hrs 15 35 4 Hrs 50
BP108P Pharmaceutical Analysis I –
Practical
5 10 4 Hrs 15 35 4 Hrs 50
BP109P Pharmaceutics I – Practical 5 10 4 Hrs 15 35 4 Hrs 50
BP110P Pharmaceutical InorganicChemistry –
Practical
5 10 4 Hrs 15 35 4 Hrs 50
BP111P Communication skills –
Practical*
5 5 2 Hrs 10 15 2 Hrs 25
BP112RBP RemedialBiology –
Practical*
5 5 2 Hrs 10 15 2 Hrs 25
Total 70/75$/80# 115/125$/130#
23/24$/26# Hrs 185/200$/210#
490/525$/
540#
31.5/33$/35#
Hrs
675/725$/
750#
7
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8. 1.Internal assessment: Continuous mode
The marks allocated for Continuous mode of Internal Assessment shall beawarded as per the scheme given below.
Table-IV :Scheme for awarding internal assessment: Continuous mode
Theory
Criteria MaximumMarks
Attendance (Refer Table – XII) 4 2
Academic activities (Average of any 3 activities e.g. quiz, assignment,open book test, field work, group
discussion and seminar)
3 1.5
Student – Teacher interaction 3 1.5
Total 10 5
Practical
Attendance (Refer Table – XII) 2
Based on Practical Records, Regular viva voce, etc. 3
Total 5
8
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9. Table- V: Guidelines for the allotment of marks for attendance
Percentage of Attendance Theory Practical
95 – 100 4 2
90 – 94 3 1.5
85 – 89 2 1
80 – 84 1 0.5
Less than 80 0 0
9
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10. Sessional Exams
Two Sessional exams shall be conducted for each theory / practical
course as per the schedule fixed by the college(s).
The scheme of question paper for theory and practical Sessional
examinations is given below.
Sessional exam shall be conducted for 30 marks for theory and shall
be computed for 15 marks.
Similarly Sessional exam for practical shall be conducted for 40
marks and shall be computed for 10 marks
10
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11. Question paper pattern for theory Sessional examinations
Table-VI
I. Multiple Choice Questions (MCQs)OR = 10 x 1 = 10
OR
Objective Type Questions (5 x 2) = 05 x 2 = 10
(Answer all the questions)
I. LongAnswers (Answer 1 out of 2) = 1 x 10 = 10
II. Short Answers (Answer 2 out of 3) = 2 x 5 = 10
Total = 30 marks
11
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12. For subjects having Non University Examination
I. Long Answers (Answer 1 out of 2) = 1 x 10 = 10
II. Short Answers (Answer 4 out of 6) = 4 x 5 = 20
Total = 30 marks
------------------
Question paper pattern for practical sessional examinations
I. Synopsis = 10
II. Experiments = 25
III. Viva voce = 05
Total = 40 marks
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Table-VII
13. Carry forward of marks
In case a student fails to secure the minimum 50% in
any theory or practical course as specified in 12,then
he/she shall reappear for the end semester
examinationof that course.
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14. Question paper pattern for end semester theory examinations.
For 75 marks paper
Table-VIII
I. Multiple Choice Questions(MCQs)
OR
= 20 x 1 = 20
OR
Objective Type Questions (10 x 2) = 10 x 2 = 20
(Answer all the questions)
II. Long Answers (Answer 2 out of 3) = 2 x 10 = 20
III. Short Answers (Answer 7 out of 9) = 7 x 5 = 35
Total = 75 marks
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15. For 50 marks paper
Table-IX
I. Long Answers (Answer 2 out of 3)
II. Short Answers (Answer 6 outof 8)
=
=
2 x 10 = 20
6 x 5 = 30
Total = 50 marks
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For 35 marks paper
I. Long Answers (Answer 1 out of 2) = 1 x 10 =10
II. Short Answers (Answer 5 out of 7) = 5 x 5 = 25
Total = 35 marks
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Question paper pattern for end semester practical examinations
I. Synopsis = 5
II. Experiments = 25
III. Viva voce = 5
Total = 35 marks
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16. Letter grades and grade points equivalent toPercentage of marks and performances
Table-X
Percentage of
Marks Obtained
Letter Grade Grade Point Performance
90.00 – 100 O 10 Outstanding
80.00 – 89.99 A 9 Excellent
70.00 – 79.99 B 8 Good
60.00 – 69.99 C 7 Fair
50.00 – 59.99 D 6 Average
Less than 50 F 0 Fail
Absent AB 0 Fail
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