Search Results for "drug development procedure"

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Dissolution chapter

Dissolution chapter

Introduction to Dissolution equipment's, Calibration of dissolution apparatus, Dissolution proce...

112 slides 13,695
Healthcare
ArshadKhan63
Models of Technology Transfer.pdf

Models of Technology Transfer.pdf

Transferring of details related to formulation and analytical strategies from one area to another ar...

14 slides 1,007
Science
ICH HARMONISED TRIPARTITE GUIDELINE - IMPURITIES IN NEW DRUG PRODUCTS Q3B(R2)

ICH HARMONISED TRIPARTITE GUIDELINE - IMPURITIES IN NEW DRUG PRODUCTS Q3B(R2)

Guidance for registration applications on the content and qualification of impurities in new drug pr...

18 slides 461
Design
EPDB - Exploratory Product Development Breif

EPDB - Exploratory Product Development Breif

DOCUMENT A DOCUMENT is a piece of written, printed, or electronic matter that provides information o...

16 slides 2,390
Technology
VanshikaGupta948537
Thin_layer_chromatography zoology pg student

Thin_layer_chromatography zoology pg student

Slide 1: Title Slide Title: Thin Layer Chromatography (TLC) in Zoology Subtitle: An Overview for Pos...

14 slides 33
Education
supravatdora456
Drug development process.

Drug development process.

DRUG DEVELOPMENT PROCESS. DETAILED DESCRIPTION OF DRUG DEVELOPMENT PROCESS. DRUG DEVELOPMENT. PHASES...

55 slides 112,437
Healthcare
Q2R1.pptx

Q2R1.pptx

ICH Q2R1 guideline of analytical method development and validation

26 slides 567
Design
ICH Q6A Specifications by Chandra Mohan

ICH Q6A Specifications by Chandra Mohan

Setting of specification limits as per ICH Q6A

61 slides 9,265
Design
Ich guidelines

Ich guidelines

ICH guidelines with Q2R1 explained in detail

19 slides 762
Design
SurbhiSharma196
impurities of new drug products based on ICH guidelines(Q3BR2)

impurities of new drug products based on ICH guidelines(Q3BR2)

IMPURITIES IN NEW DRUG PRODUCTS BASED ON ICH GUIDELINES Q3BR2. Brief note on impurities present in n...

12 slides 1,619
Design
ICH [ Q ] Guidelines

ICH [ Q ] Guidelines

OBJECTIVES AIM ICH ORGANISATION STRUCTURE ICH MEMBERS ICH VARIOUS GUIDELINES ICH GUIDELINES CATEGORI...

34 slides 9,042
Business
Ich Guidelines Au. Vivek Jain

Ich Guidelines Au. Vivek Jain

Ich guidelines syllabus accor. to PCI

33 slides 10,655
Design
VivekJain275
DRUG REGULATORY AFFAIRS

DRUG REGULATORY AFFAIRS

It includes information about regulatory bodies, role of drug Regulatory professional, countries wit...

26 slides 752
Technology
Ich quality guidelines

Ich quality guidelines

International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use

28 slides 9,206
Design
Developing Specification (ICH Q6 and Q3), Purchase specifications and maintenance of stores for raw materials

Developing Specification (ICH Q6 and Q3), Purchase specifications and maintenance of stores for raw materials

Purchase specifications are detailed guidelines that define the operational, physical, and chemical ...

61 slides 560
Technology
ICH Guidelines

ICH Guidelines

Pharmaceutical Quality Assurance B.Pharmacy Third Year Sem-VI As per PCI Syllabus

26 slides 1,865
Technology
PROCESS OF ICH (International Council for Harmonisation)

PROCESS OF ICH (International Council for Harmonisation)

In this slides contain a ICH guidelines process and information about the organization. https://www....

31 slides 9,198
Design
SwathyAmmu
Investigational new drug (IND)

Investigational new drug (IND)

drug development, IND, withdrawl of IND, exemption, IND review,

16 slides 16,291
Science
Industry and fda laision &

Industry and fda laision &

Pharmaceutical Regulataory Affairs

39 slides 4,970
Technology
Documentation in pharmaceutical industry, by dr. umesh kumar sharma and anu mathew

Documentation in pharmaceutical industry, by dr. umesh kumar sharma and anu mathew

DOCUMENTATION IN PHARMACEUTICAL INDUSTRY, BY Dr. UMESH KUMAR SHARMA

38 slides 9,578
Healthcare
Q3A(R2)

Q3A(R2)

IMPURITIES IN NEW DRUG SUBSTANCES

24 slides 10,423
General
ICH GUIDELINES Q S E M & REGULATORY REQUIREMENTS OF EU, MHRA, TGA & ROW COUNTRIES

ICH GUIDELINES Q S E M & REGULATORY REQUIREMENTS OF EU, MHRA, TGA & ROW COUNTRIES

ICH GUIDELINES Q S E M & REGULATORY REQUIREMENTS OF EU, MHRA, TGA & ROW COUNTRIES

24 slides 1,551
Design
RushikeshPalkar1
TECHNOLOGY TRANSFER PROCESS IN PHARMACEUTICAL INDUSTRIES ( IP-2/ UNIT 2)

TECHNOLOGY TRANSFER PROCESS IN PHARMACEUTICAL INDUSTRIES ( IP-2/ UNIT 2)

TECHNOLOGY TRANSFER PROCESS IN PHARMACEUTICAL INDUSTRIES

65 slides 6,299
Healthcare
ICH Q3B (R2):Impurities in new drug products

ICH Q3B (R2):Impurities in new drug products

in this slide a brief of ICH guidelines about impurities in new drug product is given .

18 slides 5,623
Design