SlideShare ist ein Scribd-Unternehmen logo
1 von 1
Downloaden Sie, um offline zu lesen
Comparing the Canadian CTA to the U.S.
                   IND Submission Process

                 Canadian CTA                                                   U.S. IND

Principle:                                               Principle:
One Clinical Trial Application (CTA) per protocol.       One open Investigational New Drug (IND) throughout
Protocol-by-protocol approval.                           drug development. New protocols submitted as
                                                         amendments.

Format:                                                  Format:
Common Technical Document (CTD)                          Common Technical Document (CTD) or
                                                         Investigational New Drug (IND) template

Review:                                                  Review:
- 30-day default review period except for Phase 1        - 30-day default period
  Bioequivalence studies (7 days)                        - Information request
- Clarification request                                  - Clinical hold
- Not Satisfactory Notice
- Receipt of a No Objection Letter (NOL)

Administrative Requirements:                             Administrative Requirements:
- Signature from Canadian representative                 - Signature from U.S. representative

Canadian Specifications:                                 U.S. Specifications:
- List ongoing Clinical Trials in Canada                 -   Introductory statement
- Clinical Trial Site Information Form (Health Canada    -   General Investigational plan
  database of on going studies and sites)                -   Investigator data (statement, CV)
- Protocol synopsis or rational product summary          -   120 days to submit audited reports
- Foreign Regulatory Authorities refusals                -   Annual report to FDA
- No annual report

CTA Amendments:                                          IND Amendments:
- Protocol amendment (30 day review):                    - Protocol amendment: similar requirements
	 •	Quality                                              - New investigator: IND amendment
	 •	Clinical                                             - Response to clinical hold (30 day review)
- New Investigator: Clinical Trial Site Information
  Form submitted
- Updated protocol with comprehensive amendment
- Notifications to Health Canada for minor protocol
  changes: Clinical Trial discontinuation, IRB refusal
  & Clinical Trial closure

Additional Information:
- Unlike INDs, there are no additional summaries to
  prepare outside the Investigator’s Brochure, i.e. no
  non-clinical or clinical reports to be submitted
- Approximate time to prepare a CTA once the
  required data has been received: 1-3 weeks
- Can be submitted at the same time, before or
  after an IND
- No review cost for CTAs in Canada



                                        www.scimega.com

Weitere ähnliche Inhalte

Was ist angesagt?

The Electronic Regulatory Submission
The Electronic Regulatory SubmissionThe Electronic Regulatory Submission
The Electronic Regulatory Submission
Dr.RAJEEV KASHYAP
 
Pros and cons of eCTD baseline submissions
Pros and cons of eCTD baseline submissionsPros and cons of eCTD baseline submissions
Pros and cons of eCTD baseline submissions
eCTDconsultancy
 

Was ist angesagt? (20)

Doc in pharma
Doc in pharmaDoc in pharma
Doc in pharma
 
Regulatory Affairs by Chandra Mohan
Regulatory Affairs by Chandra MohanRegulatory Affairs by Chandra Mohan
Regulatory Affairs by Chandra Mohan
 
Marketing Authorization Procedure in European Union
Marketing Authorization Procedure in European UnionMarketing Authorization Procedure in European Union
Marketing Authorization Procedure in European Union
 
eCTD Submission process diagramm
eCTD Submission process diagrammeCTD Submission process diagramm
eCTD Submission process diagramm
 
Regulatory requirements for drug approval in Saudi Arabia
Regulatory requirements for drug approval in Saudi ArabiaRegulatory requirements for drug approval in Saudi Arabia
Regulatory requirements for drug approval in Saudi Arabia
 
DMF CEP
DMF CEPDMF CEP
DMF CEP
 
Fundamental concept of regulatory affairs in pharmaceutical & biotechnology
Fundamental concept of regulatory affairs in pharmaceutical & biotechnologyFundamental concept of regulatory affairs in pharmaceutical & biotechnology
Fundamental concept of regulatory affairs in pharmaceutical & biotechnology
 
Drug approval process in japan
Drug approval process in japanDrug approval process in japan
Drug approval process in japan
 
International drug regulatory affairs
International drug regulatory affairsInternational drug regulatory affairs
International drug regulatory affairs
 
The Electronic Regulatory Submission
The Electronic Regulatory SubmissionThe Electronic Regulatory Submission
The Electronic Regulatory Submission
 
Pros and cons of eCTD baseline submissions
Pros and cons of eCTD baseline submissionsPros and cons of eCTD baseline submissions
Pros and cons of eCTD baseline submissions
 
Anda refuse to receive
Anda   refuse to receiveAnda   refuse to receive
Anda refuse to receive
 
drug master file
drug master filedrug master file
drug master file
 
ANDA Submissions : When will FDA Refuse to Accept an ANDA
ANDA Submissions :When will FDA Refuse  to Accept an ANDA ANDA Submissions :When will FDA Refuse  to Accept an ANDA
ANDA Submissions : When will FDA Refuse to Accept an ANDA
 
ICH GCP
ICH GCPICH GCP
ICH GCP
 
Formal Meetings between the FDA and Sponsors or Applicants
Formal Meetings between the FDA and Sponsors or ApplicantsFormal Meetings between the FDA and Sponsors or Applicants
Formal Meetings between the FDA and Sponsors or Applicants
 
African Medicines Regulatory Harmonisation
African Medicines Regulatory Harmonisation African Medicines Regulatory Harmonisation
African Medicines Regulatory Harmonisation
 
USFDA NDA Vs BLA
USFDA NDA Vs BLAUSFDA NDA Vs BLA
USFDA NDA Vs BLA
 
Post-NOC changes
Post-NOC changesPost-NOC changes
Post-NOC changes
 
Abriviated new drug application 505(j) filling
Abriviated new drug application 505(j) fillingAbriviated new drug application 505(j) filling
Abriviated new drug application 505(j) filling
 

Ähnlich wie Canadian CTA vs. U.S. IND

AllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.gov
AllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.govAllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.gov
AllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.gov
SenseAboutSci
 
Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...
Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...
Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...
cisukraine00
 
Marketing Authorization In The Eu
Marketing Authorization In The EuMarketing Authorization In The Eu
Marketing Authorization In The Eu
clarityeye
 
International Overview & Future Medical Devices Regulations
International Overview & Future   Medical Devices RegulationsInternational Overview & Future   Medical Devices Regulations
International Overview & Future Medical Devices Regulations
mdbio2009
 

Ähnlich wie Canadian CTA vs. U.S. IND (20)

INDA (INVESTIGATIONAL NEW DRUG APPLICATIONS)
INDA (INVESTIGATIONAL NEW DRUG APPLICATIONS)INDA (INVESTIGATIONAL NEW DRUG APPLICATIONS)
INDA (INVESTIGATIONAL NEW DRUG APPLICATIONS)
 
AllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.gov
AllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.govAllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.gov
AllTrials AAAS 2015 - Opportunities and Challenges for ClinicalTrials.gov
 
Clinical Trial Registries: Panacea or Pablum?
Clinical Trial Registries:  Panacea or Pablum?Clinical Trial Registries:  Panacea or Pablum?
Clinical Trial Registries: Panacea or Pablum?
 
NDA- New Drug Application
NDA- New Drug ApplicationNDA- New Drug Application
NDA- New Drug Application
 
clinical trial application in india
clinical trial application in indiaclinical trial application in india
clinical trial application in india
 
Global submission of IND, NDA ANDA ( Santosh Kumar) (1).pptx
Global submission of IND, NDA ANDA ( Santosh Kumar) (1).pptxGlobal submission of IND, NDA ANDA ( Santosh Kumar) (1).pptx
Global submission of IND, NDA ANDA ( Santosh Kumar) (1).pptx
 
INVESTIGATIONAL NEW DRUG APPLICATION(IND)
INVESTIGATIONAL NEW DRUG APPLICATION(IND) INVESTIGATIONAL NEW DRUG APPLICATION(IND)
INVESTIGATIONAL NEW DRUG APPLICATION(IND)
 
Non clinical drug development
Non clinical drug developmentNon clinical drug development
Non clinical drug development
 
Barbara Sabourin regulating drugs in canada v2
Barbara Sabourin regulating drugs in canada v2Barbara Sabourin regulating drugs in canada v2
Barbara Sabourin regulating drugs in canada v2
 
The Importance of Developing a Global Regulatory Strategy towards the Goal of...
The Importance of Developing a Global Regulatory Strategy towards the Goal of...The Importance of Developing a Global Regulatory Strategy towards the Goal of...
The Importance of Developing a Global Regulatory Strategy towards the Goal of...
 
Webinar: Clinical Trial Registration Jan 2009
Webinar: Clinical Trial Registration Jan 2009Webinar: Clinical Trial Registration Jan 2009
Webinar: Clinical Trial Registration Jan 2009
 
Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...
Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...
Global Clinical Tirals.pptx (GCP) Global Clinical Trial means any clinical tr...
 
Regulatory Highlights and Drug Development in China
Regulatory Highlights and Drug Development in ChinaRegulatory Highlights and Drug Development in China
Regulatory Highlights and Drug Development in China
 
NDA IND and ANDA
NDA IND and ANDANDA IND and ANDA
NDA IND and ANDA
 
Digital Scholar Webinar: Clinicaltrials.gov Registration and Reporting Documents
Digital Scholar Webinar: Clinicaltrials.gov Registration and Reporting DocumentsDigital Scholar Webinar: Clinicaltrials.gov Registration and Reporting Documents
Digital Scholar Webinar: Clinicaltrials.gov Registration and Reporting Documents
 
Drug Approval & Reimbursement Processes
Drug Approval & Reimbursement ProcessesDrug Approval & Reimbursement Processes
Drug Approval & Reimbursement Processes
 
Marketing Authorization In The Eu
Marketing Authorization In The EuMarketing Authorization In The Eu
Marketing Authorization In The Eu
 
Regulation of Medical Devices in US
Regulation of Medical Devices in USRegulation of Medical Devices in US
Regulation of Medical Devices in US
 
International Overview & Future Medical Devices Regulations
International Overview & Future   Medical Devices RegulationsInternational Overview & Future   Medical Devices Regulations
International Overview & Future Medical Devices Regulations
 
clinical trial Management with ethics committee
clinical trial  Management with ethics committeeclinical trial  Management with ethics committee
clinical trial Management with ethics committee
 

Mehr von Roberto Lara

Mehr von Roberto Lara (7)

The Secret to Successful Early Phase Study Expansions in Canada
The Secret to Successful Early Phase Study Expansions in CanadaThe Secret to Successful Early Phase Study Expansions in Canada
The Secret to Successful Early Phase Study Expansions in Canada
 
AACR Cancer Progress Report 2015
AACR Cancer Progress Report 2015AACR Cancer Progress Report 2015
AACR Cancer Progress Report 2015
 
What Your CRO Doesn't Know Could Hurt You
What Your CRO Doesn't Know Could Hurt YouWhat Your CRO Doesn't Know Could Hurt You
What Your CRO Doesn't Know Could Hurt You
 
Solving the operational challenges of oncology clinical trials
Solving the operational challenges of oncology clinical trialsSolving the operational challenges of oncology clinical trials
Solving the operational challenges of oncology clinical trials
 
Key Strategies to Survive in Today\’s Changing World of Oncology Clinical Trials
Key Strategies to Survive in Today\’s Changing World of Oncology Clinical TrialsKey Strategies to Survive in Today\’s Changing World of Oncology Clinical Trials
Key Strategies to Survive in Today\’s Changing World of Oncology Clinical Trials
 
Oncology Clinical Development Challenges and Opportunities in the Phase 1 Set...
Oncology Clinical Development Challenges and Opportunities in the Phase 1 Set...Oncology Clinical Development Challenges and Opportunities in the Phase 1 Set...
Oncology Clinical Development Challenges and Opportunities in the Phase 1 Set...
 
The Reverse Feasibility Program
The Reverse Feasibility ProgramThe Reverse Feasibility Program
The Reverse Feasibility Program
 

Canadian CTA vs. U.S. IND

  • 1. Comparing the Canadian CTA to the U.S. IND Submission Process Canadian CTA U.S. IND Principle: Principle: One Clinical Trial Application (CTA) per protocol. One open Investigational New Drug (IND) throughout Protocol-by-protocol approval. drug development. New protocols submitted as amendments. Format: Format: Common Technical Document (CTD) Common Technical Document (CTD) or Investigational New Drug (IND) template Review: Review: - 30-day default review period except for Phase 1 - 30-day default period Bioequivalence studies (7 days) - Information request - Clarification request - Clinical hold - Not Satisfactory Notice - Receipt of a No Objection Letter (NOL) Administrative Requirements: Administrative Requirements: - Signature from Canadian representative - Signature from U.S. representative Canadian Specifications: U.S. Specifications: - List ongoing Clinical Trials in Canada - Introductory statement - Clinical Trial Site Information Form (Health Canada - General Investigational plan database of on going studies and sites) - Investigator data (statement, CV) - Protocol synopsis or rational product summary - 120 days to submit audited reports - Foreign Regulatory Authorities refusals - Annual report to FDA - No annual report CTA Amendments: IND Amendments: - Protocol amendment (30 day review): - Protocol amendment: similar requirements • Quality - New investigator: IND amendment • Clinical - Response to clinical hold (30 day review) - New Investigator: Clinical Trial Site Information Form submitted - Updated protocol with comprehensive amendment - Notifications to Health Canada for minor protocol changes: Clinical Trial discontinuation, IRB refusal & Clinical Trial closure Additional Information: - Unlike INDs, there are no additional summaries to prepare outside the Investigator’s Brochure, i.e. no non-clinical or clinical reports to be submitted - Approximate time to prepare a CTA once the required data has been received: 1-3 weeks - Can be submitted at the same time, before or after an IND - No review cost for CTAs in Canada www.scimega.com