02:24

P-14 Synthesis of Ethosuximide || medicinal chemistry 1 || B Pharma 4th semester

01:01

P-13 Synthesis of phenytoin || medicinal chemistry 1 || B Pharma 4th semester

02:06

P-12 Synthesis of chloropramazene hydrochloride|| medicinal chemistry 1 || B Pharma 4th semester

01:31

P-11 Synthesis of Barbital || medicinal chemistry 1 || B Pharma 4th semester

01:37

P-10 Synthesis of Diazepam || medicinal chemistry 1 || B Pharma 4th semester

01:52

P-9 Synthesis of procyclidine hydrochloride || medicinal chemistry 1 || B Pharma 4th semester

40:13

MEDICINAL CHEMISTRY I || ALL 22 SYNTHESIS REACTION || B.PHARM 5TH SEMESTER

02:34

P-8 Synthesis of Dicyclomome hydrochloride || medicinal chemistry 1 || B Pharma 4th semester

00:54

P-7 Synthesis of Ipratropium bromide || medicinal chemistry 1 || B Pharma 4th semester

01:15

P-6 Synthesis of Neostigmine || medicinal chemistry 1 || B Pharma 4th semester

02:51

P- 5 Synthesis of Carbachol || medicinal chemistry 1 || B Pharma 4th semester

08:05

How to write D Pharma Exam Copy // copy presentation in exam // BTE

02:26

P- 4 Synthesis of Propranolol || medicinal chemistry 1 || B Pharma 4th semester

02:05

P - 3 Synthesis of Tolazolin || medicinal chemistry 1 || B Pharma 4th semester

02:17

P- 2 Synthesis of Salbutamol || medicinal chemistry 1 || B Pharma 4th semester

01:27

P-1 Synthesis of Phenylephrine || medicinal chemistry 1 || B Pharma 4th semester

03:33

regulatory authority of new drug approval part 25

04:50

CDSCO central drug standard control organisation part 24

05:17

ISO 9000 part 23

03:14

NABL part 21

01:49

six Sigma level part 19

02:55

quality by design part 18

09:33

new drug application part 17

01:53

FDA food drug administration part 16

03:41

clinical research part 15

06:06

type of investment new drug application part 14

02:57

non clinical drugs drugs drugs development part 13

02:49

regulatory affairs part 12

09:48

quality risk management 11

01:32

confidential agreement part 10

05:15

technology transfer protocol Part 9

06:12

who guidelines for technology transfer part 8

02:42

technology transfer part 7

12:31

SUPAC scale up post approval change part 6

03:40

plateform technology part 5

07:15

consideration for solid dosage form part 4

12:46

good manufacturing consideration part 3

02:35

purpose of pilot plant technique part 2

01:24

affinity chromatography part 23

02:51

gel chromatography part 22

06:56

Sythesis of chloramphenicol

06:58

ion exchange chromatography part 21

01:09

eddy diffusion part 20

04:30

HPLC High performance liquid chromatography part 19

11:19

electrophoresis part 18

06:35

total quality management part 20

04:07

gas chromatography part 17

01:34

paper chromatography part 16

08:10

thin layer chromatography part 15

02:29

normal and reverse chromatography part 14

03:53

chromatography part 13

01:44

nephelometry part 12

05:23

atomic absorption theory part 11

03:20

fundamentals mode of vibration part 8

09:07

infrared spectroscopy scopy part 7

03:52

out of specifications part 22

03:53

pilot plant technique part 1

07:01

Flourimetry / flourescense and phosphorescence part 6

01:04

Quenching part 5

08:40

UV visible spectroscopy scopy part 4