Submit Search
Upload
Summary Of Schedule Y
•
Download as PPT, PDF
•
61 likes
•
26,736 views
L
lekshmilnair
Follow
Report
Share
Report
Share
1 of 10
Download now
Recommended
SCHEDULE Y : Latest Amendment
SCHEDULE Y : Latest Amendment
Vishal Kumar Biswkarma
Regulations for drug approval in USA, E.U & India
Regulations for drug approval in USA, E.U & India
Dr. Pankaj Bablani
Schedule Y by akshdeep sharma
Schedule Y by akshdeep sharma
Akshdeep Sharma
Regulation Governing Clinical Trials In India,USA and Europe.
Regulation Governing Clinical Trials In India,USA and Europe.
KapilKumar198
Icmr dbt stem cell guidelines
Icmr dbt stem cell guidelines
Dr.Dinesh Shende
Comparison of Clinical Trial Application requirement of India, USA and Europe.
Comparison of Clinical Trial Application requirement of India, USA and Europe.
Aakashdeep Raval
Preparation of Clinical Trial Protocol of India.
Preparation of Clinical Trial Protocol of India.
Aakashdeep Raval
Regulatory authorities (US-FDA, WHO and ICH)
Regulatory authorities (US-FDA, WHO and ICH)
Sagar Savale
Recommended
SCHEDULE Y : Latest Amendment
SCHEDULE Y : Latest Amendment
Vishal Kumar Biswkarma
Regulations for drug approval in USA, E.U & India
Regulations for drug approval in USA, E.U & India
Dr. Pankaj Bablani
Schedule Y by akshdeep sharma
Schedule Y by akshdeep sharma
Akshdeep Sharma
Regulation Governing Clinical Trials In India,USA and Europe.
Regulation Governing Clinical Trials In India,USA and Europe.
KapilKumar198
Icmr dbt stem cell guidelines
Icmr dbt stem cell guidelines
Dr.Dinesh Shende
Comparison of Clinical Trial Application requirement of India, USA and Europe.
Comparison of Clinical Trial Application requirement of India, USA and Europe.
Aakashdeep Raval
Preparation of Clinical Trial Protocol of India.
Preparation of Clinical Trial Protocol of India.
Aakashdeep Raval
Regulatory authorities (US-FDA, WHO and ICH)
Regulatory authorities (US-FDA, WHO and ICH)
Sagar Savale
OVERVIEW OF DRUG REGULATORY AGENCIES IN INDIA, USA, EUROPE AND JAPAN
OVERVIEW OF DRUG REGULATORY AGENCIES IN INDIA, USA, EUROPE AND JAPAN
Arul Packiadhas
Medical device regulation US, European Union and India
Medical device regulation US, European Union and India
CSIR-URDIP, NCL Campus, Pune
Medical device regulations in india
Medical device regulations in india
Suraj Pamadi
institutional review board and independent ethics committee
institutional review board and independent ethics committee
MOHAMMAD ASIM
Quality, Safety and Legislation of Herbal Products in India
Quality, Safety and Legislation of Herbal Products in India
S S N D Balakrishna Ch
CONTRACT RESEARCH ORGANIZATION
CONTRACT RESEARCH ORGANIZATION
Raghavendra institute of pharmaceutical education and research .
Schedule y
Schedule y
kumargourav40
ICH GCP
ICH GCP
Tamer Hifnawy
Medical Dictionary for Regulatory Activities (MedDRA)
Medical Dictionary for Regulatory Activities (MedDRA)
SMS MEDICAL COLLEGE
Regulatory authority of japan
Regulatory authority of japan
AadityaThole
Ich e6(r1)
Ich e6(r1)
ManishaChauhan86
Schedule y
Schedule y
pharmacologyseminars
Schedule y
Schedule y
Malla Reddy College of Pharmacy
Schedule Y
Schedule Y
Parul Institute of Pharmacy
Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator
MOHAMMEDSALEEMJM
Regulation in clinical trial, Schedule Y and recent amendments
Regulation in clinical trial, Schedule Y and recent amendments
Dr. Siddhartha Dutta
ICH GCP
ICH GCP
PAREXEL International Clinical Research
Ethical guidelines for biomedical research in human participants
Ethical guidelines for biomedical research in human participants
gangireddysaisneha
Institutional review board/Independent ethics Committee
Institutional review board/Independent ethics Committee
ChintamBaladattaSai
Clinical trial phases, requirements and regulations
Clinical trial phases, requirements and regulations
Dr. Siddhartha Dutta
Schedule Y
Schedule Y
kamalakar ambati
Schedule Y
Schedule Y
Fardan Qadeer
More Related Content
What's hot
OVERVIEW OF DRUG REGULATORY AGENCIES IN INDIA, USA, EUROPE AND JAPAN
OVERVIEW OF DRUG REGULATORY AGENCIES IN INDIA, USA, EUROPE AND JAPAN
Arul Packiadhas
Medical device regulation US, European Union and India
Medical device regulation US, European Union and India
CSIR-URDIP, NCL Campus, Pune
Medical device regulations in india
Medical device regulations in india
Suraj Pamadi
institutional review board and independent ethics committee
institutional review board and independent ethics committee
MOHAMMAD ASIM
Quality, Safety and Legislation of Herbal Products in India
Quality, Safety and Legislation of Herbal Products in India
S S N D Balakrishna Ch
CONTRACT RESEARCH ORGANIZATION
CONTRACT RESEARCH ORGANIZATION
Raghavendra institute of pharmaceutical education and research .
Schedule y
Schedule y
kumargourav40
ICH GCP
ICH GCP
Tamer Hifnawy
Medical Dictionary for Regulatory Activities (MedDRA)
Medical Dictionary for Regulatory Activities (MedDRA)
SMS MEDICAL COLLEGE
Regulatory authority of japan
Regulatory authority of japan
AadityaThole
Ich e6(r1)
Ich e6(r1)
ManishaChauhan86
Schedule y
Schedule y
pharmacologyseminars
Schedule y
Schedule y
Malla Reddy College of Pharmacy
Schedule Y
Schedule Y
Parul Institute of Pharmacy
Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator
MOHAMMEDSALEEMJM
Regulation in clinical trial, Schedule Y and recent amendments
Regulation in clinical trial, Schedule Y and recent amendments
Dr. Siddhartha Dutta
ICH GCP
ICH GCP
PAREXEL International Clinical Research
Ethical guidelines for biomedical research in human participants
Ethical guidelines for biomedical research in human participants
gangireddysaisneha
Institutional review board/Independent ethics Committee
Institutional review board/Independent ethics Committee
ChintamBaladattaSai
Clinical trial phases, requirements and regulations
Clinical trial phases, requirements and regulations
Dr. Siddhartha Dutta
What's hot
(20)
OVERVIEW OF DRUG REGULATORY AGENCIES IN INDIA, USA, EUROPE AND JAPAN
OVERVIEW OF DRUG REGULATORY AGENCIES IN INDIA, USA, EUROPE AND JAPAN
Medical device regulation US, European Union and India
Medical device regulation US, European Union and India
Medical device regulations in india
Medical device regulations in india
institutional review board and independent ethics committee
institutional review board and independent ethics committee
Quality, Safety and Legislation of Herbal Products in India
Quality, Safety and Legislation of Herbal Products in India
CONTRACT RESEARCH ORGANIZATION
CONTRACT RESEARCH ORGANIZATION
Schedule y
Schedule y
ICH GCP
ICH GCP
Medical Dictionary for Regulatory Activities (MedDRA)
Medical Dictionary for Regulatory Activities (MedDRA)
Regulatory authority of japan
Regulatory authority of japan
Ich e6(r1)
Ich e6(r1)
Schedule y
Schedule y
Schedule y
Schedule y
Schedule Y
Schedule Y
Roles and Responsibilities of sponsor, CRO, and investigator
Roles and Responsibilities of sponsor, CRO, and investigator
Regulation in clinical trial, Schedule Y and recent amendments
Regulation in clinical trial, Schedule Y and recent amendments
ICH GCP
ICH GCP
Ethical guidelines for biomedical research in human participants
Ethical guidelines for biomedical research in human participants
Institutional review board/Independent ethics Committee
Institutional review board/Independent ethics Committee
Clinical trial phases, requirements and regulations
Clinical trial phases, requirements and regulations
Viewers also liked
Schedule Y
Schedule Y
kamalakar ambati
Schedule Y
Schedule Y
Fardan Qadeer
Schedule y
Schedule y
Malla Reddy College of Pharmacy
Schedule y -_priti_gupta
Schedule y -_priti_gupta
Priti Gupta
Emea
Emea
Ranjeet Singh
Code of federal regulations {cfr}
Code of federal regulations {cfr}
Nipun Gupta
Cdsco- a regulatory overview
Cdsco- a regulatory overview
Vivekanandan S
CDSCO and ADR reporting in India
CDSCO and ADR reporting in India
kiran pala
Schedule y, mk sharma
Schedule y, mk sharma
SHARDA UNIVERSITY
21 CFR PART 11
21 CFR PART 11
Dipak Patel
Schedule Y
Schedule Y
Kirti Krishna
Pharmacovigilance full information
Pharmacovigilance full information
Ravindra Kumar
Viewers also liked
(12)
Schedule Y
Schedule Y
Schedule Y
Schedule Y
Schedule y
Schedule y
Schedule y -_priti_gupta
Schedule y -_priti_gupta
Emea
Emea
Code of federal regulations {cfr}
Code of federal regulations {cfr}
Cdsco- a regulatory overview
Cdsco- a regulatory overview
CDSCO and ADR reporting in India
CDSCO and ADR reporting in India
Schedule y, mk sharma
Schedule y, mk sharma
21 CFR PART 11
21 CFR PART 11
Schedule Y
Schedule Y
Pharmacovigilance full information
Pharmacovigilance full information
Similar to Summary Of Schedule Y
Schedule Y Summary
Schedule Y Summary
Shrinath Sonwane
Schedule y draft 2
Schedule y draft 2
Malla Reddy College of Pharmacy
Seminar schedule 'y'
Seminar schedule 'y'
SameerKhasbage
Schedule y jjjjjjjjjjjjjjjjjjjppt
Schedule y jjjjjjjjjjjjjjjjjjjppt
Malla Reddy College of Pharmacy
Schedule Y
Schedule Y
Richa Patel
Schedule Y-2019
Schedule Y-2019
Devang Rana
Dr.s.s amended schedule y
Dr.s.s amended schedule y
National Institute of Biologics
Schedule y
Schedule y
AMRUTHA JOSE
INDA/NDA/ANDA
INDA/NDA/ANDA
Rohit Bhosale
PART 1 _ Documentation of drug trials and regulatory filings (1).pptx
PART 1 _ Documentation of drug trials and regulatory filings (1).pptx
DilsarGohil1
schedule y of drugs and cosmetic acts
schedule y of drugs and cosmetic acts
arponbiswas
INDA- Investigation New Drug Application
INDA- Investigation New Drug Application
Dr. Jigar Vyas
Schedule y under drugs and cosmetic act 1945
Schedule y under drugs and cosmetic act 1945
neelotpal31
schedule y
schedule y
pharmacologyseminars
Post marketing surveillance
Post marketing surveillance
Dhruvi50
Schedule y
Schedule y
Ashishkumar Baheti
Worldwide comprehensive study of guideline on clinical trial
Worldwide comprehensive study of guideline on clinical trial
RGPV BHOPAL
Dcgi adverse event
Dcgi adverse event
Prabir Chatterjee
BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory)2. unit ii, chapter-1 reg...
BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory)2. unit ii, chapter-1 reg...
Audumbar Mali
Indstudies
Indstudies
DollyChauhan10
Similar to Summary Of Schedule Y
(20)
Schedule Y Summary
Schedule Y Summary
Schedule y draft 2
Schedule y draft 2
Seminar schedule 'y'
Seminar schedule 'y'
Schedule y jjjjjjjjjjjjjjjjjjjppt
Schedule y jjjjjjjjjjjjjjjjjjjppt
Schedule Y
Schedule Y
Schedule Y-2019
Schedule Y-2019
Dr.s.s amended schedule y
Dr.s.s amended schedule y
Schedule y
Schedule y
INDA/NDA/ANDA
INDA/NDA/ANDA
PART 1 _ Documentation of drug trials and regulatory filings (1).pptx
PART 1 _ Documentation of drug trials and regulatory filings (1).pptx
schedule y of drugs and cosmetic acts
schedule y of drugs and cosmetic acts
INDA- Investigation New Drug Application
INDA- Investigation New Drug Application
Schedule y under drugs and cosmetic act 1945
Schedule y under drugs and cosmetic act 1945
schedule y
schedule y
Post marketing surveillance
Post marketing surveillance
Schedule y
Schedule y
Worldwide comprehensive study of guideline on clinical trial
Worldwide comprehensive study of guideline on clinical trial
Dcgi adverse event
Dcgi adverse event
BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory)2. unit ii, chapter-1 reg...
BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory)2. unit ii, chapter-1 reg...
Indstudies
Indstudies
Summary Of Schedule Y
1.
SUMMARY OF SCHEDULE
Y By Lekshmi.L.Nair
2.
3.
4.
5.
6.
7.
8.
9.
10.
Download now
![What is schedule y? ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]](data:image/gif;base64,R0lGODlhAQABAIAAAAAAAP///yH5BAEAAAAALAAAAAABAAEAAAIBRAA7)