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The International Conference on Harmonization of
Technical Requirements for Registration of
Pharmaceuticals for Human U...
* GCP born in USA – mid 1970s
* Rigorous IND procedures enforced
* Various national GCPs

USA + Europe + Japan

ICH GCP
1.
2.
I.
II.
A.
B.

European Commission
European Federation of
Pharmaceutical Industries’
Associations (EFPIA)
Ministry of...
*Birth of ICH took place at a meeting in April

1990, hosted by the EFPIA in Brussels
*Europe, Japan and the USA met
*To p...
*
*1930s – Sulfanilamide tragedy

Sulfonilamide+diethelene glycol
*1960s – Thalidomide tragedy
*1960s & 1970s

* Rapid inc...
*
Avoid duplication in tests to conform to different
regulatory guidelines
* More effective utilization of results
* Timel...
*The Early Meetings
*Terms of Reference were agreed and it was decided

that the Topics selected for harmonization would b...
*
*Where is the ICH
located

*ICH does not have "offices" as such

because it is a voluntary cooperative
effort of cosponsor...
*How is ICH

structured?

* The ICH structure consists of the

*ICH Steering Committee,
*ICH Coordinators,
*ICH Secretaria...
*
*Efficacy - 12 topic headings/14 guidelines
*Safety - 7 topic headings/14 guidelines
*Quality - 7 topic headings/19 guid...
* Safety Guidelines(animal
studies/Pre clinical
studies )

* Carcinogenicity Studies
* Genotoxicity Studies
* Toxicokineti...
*Quality Topics
*Stability
*Analytical Validation
*Impurities
*Pharmacopoeias
*Quality of Biotechnological

Products
*Spec...
*Efficacy guidelines (Clinical

studies)

*Clinical Safety
*Clinical Study Reports
*Dose-Response Studies
*Ethnic factors
...
*M "Multidisciplinary" Topics
*Cross-cutting Topics which do not fit uniquely
into one of the above categories.

*M1: Medi...
*
*
*Good Clinical Practices (GCP) is an international ethical &
scientific quality standard for designing, conducting, reco...
*
Section 1- Glossary of various terms, eg...

* Adverse drug reaction & Adverse Event
*Case report form & Clinical Study ...
*
*Monitoring & Monitoring report
*Protocol & Protocol Amendment
*Serious Adverse Event
*Source data & Source documents
*S...
*
Section 2- Principles of ICH-GCP.
2.1 Clinical Trials should be conducted in accordance with the
ethical principles cons...
ICH GCP-Section 2 Cont..
2.3 The rights, safety, and well being of the trial subjects are the
most important consideration...
ICH GCP-Section 2 Cont..
2.6 Trial should be conducted in compliance with the protocol

that has received prior institutio...
ICH GCP-Section 2 Cont..
2.9 Freely given informed consent should be obtained from
every subject prior to clinical trial p...
ICH GCP-Section 2 Cont..
2.12 Investigational products should be manufactured, handled
and stored in accordance with appli...
*
Institutional Review Boards/ Independent Ethics
Committee
*
*Should safeguard the rights, safety & well being of all trial

subjects.
*Should obtains following Documents: Protocol ...
Section 3.1: IRB/IEC Responsibilities
Cont..

*should conduct continuing review of each ongoing trial at
intervals appropr...
*
*At least 5 members
*At least one non scientific member
*At least one independent member
*Maintain list of members and q...
*
The IRB/IEC should establish, document in writing, and follow
its procedures, which should include

* Composition
* Meet...
*
*The IRB/IEC should retain all relevant records (e.g., written
procedures, membership lists, lists of occupations/affili...
*
Investigator
*
*Qualified (documented) by education, training & experience to
assume responsibility for proper trial conduct

*Should b...
*
*Potential for recruitment
*Sufficient time for trial conduct and completion
*Staff, facilities
*Ensure training to staf...
*
*Qualified physician investigator/sub investigator for the trial,
should be responsible for all trial related medical de...
*
*Written & dated approval for trial protocol, ICD,
recruitment procedures etc prior to trial initiation

*Should provide...
*
*Should conduct trial in accordance with the protocol

version agreed & documented by the sponsor, IRB and
regulatory au...
*
*Responsible for accountability at site
*May be assigned to pharmacist/individual
*Stored as specified by sponsor or reg...
*
*Should follow the trial’s randomization procedure
*Any premature unblinding to be explained to sponsor
*
*Comply with regulatory requirement, GCP and ethical
principles

*Documented Communication of revised ICD to IRB and pat...
Section 4.8: Informed Consent
cont..

*Ample time for consent and opportunity for questions
*Impartial witness for illiter...
*
*Should ensure accuracy, completeness, legibility and timeliness
of data to sponsor in CRF
*Correction in CRF should be ...
*
*The investigator should submit written summaries of the trial
status to the IRB/IEC annually, or more frequently, if re...
*
*SAE should be reported immediately to sponsor, and timely
as required to IRB/regulatory agency
*Adverse events and/or l...
*
If the trial is prematurely terminated or suspended for any
reason , Investigator :

*Should inform subjects
*Should ass...
*
*Upon completion, should inform institution, IRB, and
regulatory authorities with a summary of the trial’s outcome
*
Sponsor Responsibilities
*
*An individual, company, institution, or organization which

takes responsibility for the initiation, management, and/or...
*
*Implementing & maintaining QA and QC systems with written
SOPs to ensure GCP compliance

*Securing agreements from all ...
*
A person or an organization (commercial, academic, or other)
contracted by the sponsor to perform one or more of a spons...
*
*Designate Medical Expertise :who will be readily available to
advise on trial related medical questions or problems. (S...
*
*Information on investigational product (Section 5.12)
*Manufacturing, labeling, packaging & coding of product
(Section ...
*
*The act of overseeing the progress of a clinical trial, and of
ensuring that it is conducted, recorded, and reported in...
*
*Audit (Section 5.19)
*Noncompliance (Section 5.20)
*Premature Termination or Suspension of a Trial (Section5.21)
*Multi...
*
CLINICAL TRIAL PROTOCOL
AND
PROTOCOL AMENDMENT(S)
*
*Document describing all aspects of the study
*Well designed and thoroughly considered
*Well structured
*Complete
*
*General Information (Section 6.1)
*Background Information (Section 6.2)
*Trial Objectives and Purpose (Section 6.3)
*Tr...
*
*Statistics (Section 6.9)
*Direct Access to Source Data/Documents (Section 6.10)
*Quality Control and Quality Assurance ...
*
*Protocol Title, identifying number & date. Amendment number
*Contact names, addresses
*Name and title of Authorized sig...
*
*Aims & objectives, phase of study
*Name & description of Inv product
*Summary of non clinical & clinical studies
*Summa...
*
*Primary & secondary endpoints
*Randomized/comparator/blinded/open, placebo controlled
*Blinding technique(double blind/...
*
*Proposed date of initiation of study
*Discontinuation criteria for subjects
*Instructions on suspending or terminating ...
*

Selection and Withdrawal of Subjects

Inclusion/ Exclusion criteria:

*Specifications of the subjects to be included (a...
*
*Specifications of efficacy parameters
*Descriptions of how these are measured and recorded
*Time & periodicity of recor...
*
*Description of statistical methods employed
*Timing of interim analysis, if any
*Details of enrollment plan
*Significan...
*
*The sponsor should ensure that it is specified in the protocol or
other written agreement that the investigator(s)/inst...
*
*Steps & procedures for monitoring study
*Instructions for protocol deviations
*Allocation of duties & responsibilities ...
*
*Description of how patients/volunteers would be informed
*

*Procedures for handling & processing records of
effects and adverse events

*Handling of Products:
* Safe handling and...
*
*Budget, financial aspects
*Sources of economic support
*Subject payments
*Reimbursement to team members
*Insurance deta...
*
Informed Consent
*
*Compilation of the clinical and nonclinical data on the
investigational product that are relevant to the study of the
p...
*
* Introduction
Definition
Purpose
Information form
Edition
Type & extent
Review & revise
Up-date
* General consid...
*
ESSENTIAL DOCUMENTS FOR THE CONDUCT OF A
CLINICAL TRIAL
* Sec 8: Essential Documents -Introduction
*Essential Documents are those documents which individually
and collectively pe...
* Essential Documents to be Kept before Trial
Commences
Investigators Brochure
Signed protocols, amendments (if any) and...
* Essential Documents to be Kept before Trial
Commences
CV of investigator and sub-investigators evidencing qualification...
* Essential Documents to be Kept During the Trial
Investigator’s brochure updates
Any revisions to:
Protocol, amendment...
*
Curriculum Vitae of new investigators and sub-investigators
Updates to normal value(s) range(s) for medical lab techni...
*
Notification by the originating investigator to sponsor of serious adverse evens and
related reports

Notification by ...
* Essential Documents to be Kept
After Completion or Termination of the Trial
Investigational product(s) accountability a...
*
* Indian GCP :Dec 2001
Expert Committee set up by Central Drugs Standard Control
Organization (CDSCO) in consultation with...
* STRUCTURE
ICH E6

* Glossary
* Principles
* IRB/IEC
* Investigator
* Sponsor
* Protocol
* Investigators’ Brochure
* Esse...
ICH and GCP by Naveen
ICH and GCP by Naveen
ICH and GCP by Naveen
ICH and GCP by Naveen
ICH and GCP by Naveen
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ICH and GCP by Naveen

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ICH guidelines and its history with details of GCP in Clinical Trials

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Transcript of "ICH and GCP by Naveen"

  1. 1. *
  2. 2. * The International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH)
  3. 3. * GCP born in USA – mid 1970s * Rigorous IND procedures enforced * Various national GCPs USA + Europe + Japan ICH GCP
  4. 4. 1. 2. I. II. A. B. European Commission European Federation of Pharmaceutical Industries’ Associations (EFPIA) Ministry of Health, Labor and Welfare (MHLW) Japanese Pharmaceutical Manufacturers Association (JPMA) Food & Drug Administration (FDA) Pharmaceutical Research and Manufacturers of America (PhRMA)
  5. 5. *Birth of ICH took place at a meeting in April 1990, hosted by the EFPIA in Brussels *Europe, Japan and the USA met *To plan an International Conference but the meeting also discussed the wider implications and terms of reference of ICH. *The ICH Steering Committee which was established at that meeting has since met at least twice a year, with the location rotating between the three regions.
  6. 6. * *1930s – Sulfanilamide tragedy Sulfonilamide+diethelene glycol *1960s – Thalidomide tragedy *1960s & 1970s * Rapid increase in laws, regulations & guidelines * Industry marketing – Global * Basic evaluation – similar * Detailed technical requirements – varied
  7. 7. * Avoid duplication in tests to conform to different regulatory guidelines * More effective utilization of results * Timely access of patients to safe and effective new drugs * Promote public health * Minimize animal testing without compromising safety & effectiveness * OBJECTIVE -Elimination of unnecessary delay in global development -Make new medicines available while maintaining safeguards on -quality, safety, and efficacy, and regulatory obligations to - protect public health -More economical use of human, animal and material resources
  8. 8. *The Early Meetings *Terms of Reference were agreed and it was decided that the Topics selected for harmonization would be divided into Safety, Quality and Efficacy to reflect the three criteria which are the basis for approving and authorizing new medicinal products *It was also agreed that six-party Expert Working Groups (EWGs) should be set up to discuss scientific and technical aspects of each harmonization Topic
  9. 9. *
  10. 10. *Where is the ICH located *ICH does not have "offices" as such because it is a voluntary cooperative effort of cosponsors from the three regions. *The ICH Secretariat is based in Geneva. *The biennial meetings and conferences of the ICH Steering Committee rotate between the EU, Japan, and the USA.
  11. 11. *How is ICH structured? * The ICH structure consists of the *ICH Steering Committee, *ICH Coordinators, *ICH Secretariat and *ICH Working Groups.
  12. 12. * *Efficacy - 12 topic headings/14 guidelines *Safety - 7 topic headings/14 guidelines *Quality - 7 topic headings/19 guidelines *Medical Dictionary - MedDRA *Electronic Standards - ESTRI, E2B *Industry proposed taking the information generated by these harmonized guidances and putting it the same order
  13. 13. * Safety Guidelines(animal studies/Pre clinical studies ) * Carcinogenicity Studies * Genotoxicity Studies * Toxicokinetics and Pharmacokinetics * Toxicity Testing * Reproductive Toxicology * Biotechnological Products * Pharmacology Studies * Immunotoxicology Studies * Joint Safety/Efficacy (Multidisciplinary) Topic
  14. 14. *Quality Topics *Stability *Analytical Validation *Impurities *Pharmacopoeias *Quality of Biotechnological Products *Specifications *Good Manufacturing Practice *Pharmaceutical Development *Quality Risk Management
  15. 15. *Efficacy guidelines (Clinical studies) *Clinical Safety *Clinical Study Reports *Dose-Response Studies *Ethnic factors *Good Clinical Practice *Clinical Trials on special population *Guidelines for Clinical Evaluation by Therapeutic Category *Clinical Evaluation-( statistical consideration) *Pharmacogenomics
  16. 16. *M "Multidisciplinary" Topics *Cross-cutting Topics which do not fit uniquely into one of the above categories. *M1: Medical Terminology (MedDRA) *M2: Electronic Standards for Transmission of Regulatory Information (ESTRI) *M3: Timing of Pre-clinical Studies in Relation to Clinical Trials *M4: The Common Technical Document (CTD) *M5: Data Elements and Standards for Drug Dictionaries
  17. 17. *
  18. 18. * *Good Clinical Practices (GCP) is an international ethical & scientific quality standard for designing, conducting, recording & reporting trials that involve the participation of human subjects. *Compliance with this standard provides public assurance that rights, safety & well being of trial subjects are protected, consistent with the principles that have their origin in the declaration of Helsinki, and that the clinical trial data are credible
  19. 19. * Section 1- Glossary of various terms, eg... * Adverse drug reaction & Adverse Event *Case report form & Clinical Study Report *Coordinating Committee & Contract Research Organization *Independent Ethics Committee & Institutional Review Board *Investigator & Investigator’s Brochure
  20. 20. * *Monitoring & Monitoring report *Protocol & Protocol Amendment *Serious Adverse Event *Source data & Source documents *Sponsor & Sponsor investigator *Standard Operating Procedures *Vulnerable subjects
  21. 21. * Section 2- Principles of ICH-GCP. 2.1 Clinical Trials should be conducted in accordance with the ethical principles consistent with GCP and applicable regulatory requirements 2.2 Before a trial is initiated, forseeable risks & inconveniences should be weighed against anticipated benefit for the trial subject & society.
  22. 22. ICH GCP-Section 2 Cont.. 2.3 The rights, safety, and well being of the trial subjects are the most important considerations & should prevail over interests of science and society 2.4 The available nonclinical & clinical information on an investigational product should be adequate support the proposed clinical trial. 2.5Clinical trials should be scientifically sound, and described in a clear, detailed protocol.
  23. 23. ICH GCP-Section 2 Cont.. 2.6 Trial should be conducted in compliance with the protocol that has received prior institutional review board (IRB)/ independent ethics committee (IEC) approval/favourable opinion. 2.7 The medical care and medical decisions for subjects should be the responsibility of a qualified physician 2.8 Each individual involved in conducting a trial should be qualified by education, training & experience to perform his respective task
  24. 24. ICH GCP-Section 2 Cont.. 2.9 Freely given informed consent should be obtained from every subject prior to clinical trial participation 2.10 All clinical information should be recorded, handled, and stored in a way that allows its accurate reporting, interpretation and verification 2.11 The confidentiality of records that could identify patients should be protected, respecting the privacy and confidentiality rules in accordance with the applicable regulatory requirements
  25. 25. ICH GCP-Section 2 Cont.. 2.12 Investigational products should be manufactured, handled and stored in accordance with applicable GMP, and used in accordance with the protocol 2.13 Systems with procedures that assure the quality of every aspect of the trial should be implemented
  26. 26. * Institutional Review Boards/ Independent Ethics Committee
  27. 27. * *Should safeguard the rights, safety & well being of all trial subjects. *Should obtains following Documents: Protocol & their amendments, Patient Information sheet & consent form, subject recruitment procedures (e.g. advertisements), Investigator's Brochure (IB), available safety information, information about payments and compensation available to subjects, the investigator’s current curriculum vitae and/or other documentation evidencing qualifications, and any other documents that the IRB/IEC may need to fulfil its responsibilities
  28. 28. Section 3.1: IRB/IEC Responsibilities Cont.. *should conduct continuing review of each ongoing trial at intervals appropriate to the degree of risk to human subjects, but at least once per year. *Review Protocol/ ICD/ recruitment procedures/ IB/payments *Continuing review for Ongoing Progress/Adverse events
  29. 29. * *At least 5 members *At least one non scientific member *At least one independent member *Maintain list of members and qualifications *Only independent members to vote *Quorum to be present
  30. 30. * The IRB/IEC should establish, document in writing, and follow its procedures, which should include * Composition * Meeting Scheduling & conduct * Specify that trial starts only after IRB review * Specify regarding changes in protocol * Specify prompt reporting of adverse events
  31. 31. * *The IRB/IEC should retain all relevant records (e.g., written procedures, membership lists, lists of occupations/affiliations of members, submitted documents, minutes of meetings, and correspondence) for a period of at least 3 years after completion of the trial and make them available upon request from the regulatory authority(ies). *The IRB/IEC may be asked by investigators, sponsors or regulatory authorities to provide its written procedures and membership lists.
  32. 32. * Investigator
  33. 33. * *Qualified (documented) by education, training & experience to assume responsibility for proper trial conduct *Should be familiar with the appropriate use of the investigational product, IB, and other information provided by sponsor *Should be aware of, & should comply with, GCP and the applicable regulatory requirements *Should permit monitoring, auditing and inspection *Delegation of duties to appropriately qualified persons
  34. 34. * *Potential for recruitment *Sufficient time for trial conduct and completion *Staff, facilities *Ensure training to staff
  35. 35. * *Qualified physician investigator/sub investigator for the trial, should be responsible for all trial related medical decisions *Adequate medical care during and after trail participation *Make reasonable efforts ascertaining for premature withdrawal from trial
  36. 36. * *Written & dated approval for trial protocol, ICD, recruitment procedures etc prior to trial initiation *Should provide latest copies of IB to IRB *Should provide all relevant documents for review during trial
  37. 37. * *Should conduct trial in accordance with the protocol version agreed & documented by the sponsor, IRB and regulatory authority *No changes allowed in the protocol except in case of immediate hazard to the patient; which should be submitted to all immediately
  38. 38. * *Responsible for accountability at site *May be assigned to pharmacist/individual *Stored as specified by sponsor or regulatory authority *Used only in accordance with the protocol
  39. 39. * *Should follow the trial’s randomization procedure *Any premature unblinding to be explained to sponsor
  40. 40. * *Comply with regulatory requirement, GCP and ethical principles *Documented Communication of revised ICD to IRB and patient *No influence or coercion to participate *Subject or their legal representative should be fully informed in their own language *Non technical language
  41. 41. Section 4.8: Informed Consent cont.. *Ample time for consent and opportunity for questions *Impartial witness for illiterate patients *Subject should receive a copy of the signed and dated ICD/ amendment
  42. 42. * *Should ensure accuracy, completeness, legibility and timeliness of data to sponsor in CRF *Correction in CRF should be signed, dated *Maintain trial related documents *Financial agreements in place *Access to records by monitor, regulatory agency or auditors *Progress reports to IRB
  43. 43. * *The investigator should submit written summaries of the trial status to the IRB/IEC annually, or more frequently, if requested by the IRB/IEC. *The investigator should promptly provide written reports to the sponsor, the IRB/IEC (see 3.3.8) and, where applicable, the institution on any changes significantly affecting the conduct of the trial, and/or increasing the risk to subjects
  44. 44. * *SAE should be reported immediately to sponsor, and timely as required to IRB/regulatory agency *Adverse events and/or laboratory abnormalities identified in the protocol as critical to safety evaluations should be reported to the sponsor according to the reporting requirements and within the time periods specified by the sponsor in the protocol. *For reported deaths, the investigator should supply the sponsor and the IRB/IEC with any additional requested information (e.g., autopsy reports and terminal medical reports).
  45. 45. * If the trial is prematurely terminated or suspended for any reason , Investigator : *Should inform subjects *Should assure therapy and follow up *Should inform regulatory authorities *Should inform sponsor/IRB with explanation
  46. 46. * *Upon completion, should inform institution, IRB, and regulatory authorities with a summary of the trial’s outcome
  47. 47. * Sponsor Responsibilities
  48. 48. * *An individual, company, institution, or organization which takes responsibility for the initiation, management, and/or financing of a clinical trial
  49. 49. * *Implementing & maintaining QA and QC systems with written SOPs to ensure GCP compliance *Securing agreements from all sites for monitoring, auditing, and inspections *QC of data handling *Payment agreements
  50. 50. * A person or an organization (commercial, academic, or other) contracted by the sponsor to perform one or more of a sponsor’s trial related duties and functions *Sponsor may transfer all or some duties to CRO *Ultimate responsibility for quality lies with the sponsor *Document of all duty delegation required
  51. 51. * *Designate Medical Expertise :who will be readily available to advise on trial related medical questions or problems. (Section 5.3) *Trial design (Section.5.4), Trial management, Data handling and Record Keeping (Section 5.5) and Investigator selection (Section 5.6), Allocation of Responsibilities (Section 5.7) *Compensation to Subjects and Investigators (Section 5.8), Financing (Section 5.9) *Submission to regulatory authorities (Section 5.10) *Confirmation of review by IRBs (Section5.11)
  52. 52. * *Information on investigational product (Section 5.12) *Manufacturing, labeling, packaging & coding of product (Section 5.13) *Supplying and Handling Investigational Product(s) (Section 5.14) and Record Assess (Section 5.15) *Safety Evaluation (Section 5.16) and Adverse Drug Reaction Reporting (Section 5.17) *Monitoring (Section 5.18)
  53. 53. * *The act of overseeing the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, SOPs, GCP, and the applicable regulatory requirements
  54. 54. * *Audit (Section 5.19) *Noncompliance (Section 5.20) *Premature Termination or Suspension of a Trial (Section5.21) *Multicentre Trials (Section 5.22)
  55. 55. * CLINICAL TRIAL PROTOCOL AND PROTOCOL AMENDMENT(S)
  56. 56. * *Document describing all aspects of the study *Well designed and thoroughly considered *Well structured *Complete
  57. 57. * *General Information (Section 6.1) *Background Information (Section 6.2) *Trial Objectives and Purpose (Section 6.3) *Trial Design (Section 6.4) *Selection and Withdrawal of Subjects (Section 6.5) *Treatment of Subjects (Section 6.6) *Assessment of Efficacy (Section 6.7) *Assessment of safety (Section 6.8)
  58. 58. * *Statistics (Section 6.9) *Direct Access to Source Data/Documents (Section 6.10) *Quality Control and Quality Assurance (section 6.11) * Ethics (section 6.12) *Data handling & management (Section 6.13) *Financing and Insurance (Section 6.14) *Publication Policy (Section 6.15) *Supplements (Section 6.16)
  59. 59. * *Protocol Title, identifying number & date. Amendment number *Contact names, addresses *Name and title of Authorized signatory *Contact medical expert *Contact investigator(s) *Institution(s), Laboratories, department contact
  60. 60. * *Aims & objectives, phase of study *Name & description of Inv product *Summary of non clinical & clinical studies *Summary of risks & benefits *Description of route of administration, dosage *Statement of GCP compliance
  61. 61. * *Primary & secondary endpoints *Randomized/comparator/blinded/open, placebo controlled *Blinding technique(double blind/single blind) *Randomization(method & procedure) *Diagram of design, procedure & stages *Medications permitted & not permitted during study *Description of study treatments, dose, route during study conduct *Packing/labeling description *Duration of subject participation & sequence of all study periods, including follow up
  62. 62. * *Proposed date of initiation of study *Discontinuation criteria for subjects *Instructions on suspending or terminating the study *Procedures for monitoring compliance
  63. 63. * Selection and Withdrawal of Subjects Inclusion/ Exclusion criteria: *Specifications of the subjects to be included (age, gender, ethnic groups, prognostic factors, diagnostic criteria) *Specify exclusion criteria *Subject withdrawal criteria & procedures
  64. 64. * *Specifications of efficacy parameters *Descriptions of how these are measured and recorded *Time & periodicity of recording *Description of special analysis/ tests (PK, clinical, lab, radiology) *Specifications of safety parameters *Procedures for eliciting reports of and reporting ADR *Time &method of recording *Type, duration of follow up after adverse events)
  65. 65. * *Description of statistical methods employed *Timing of interim analysis, if any *Details of enrollment plan *Significance level, power *Procedures for reporting any deviations from the original statistical plan *Selection of subjects to be included in final analysis
  66. 66. * *The sponsor should ensure that it is specified in the protocol or other written agreement that the investigator(s)/institution(s) will permit trial-related monitoring, audits, IRB/IEC review, and regulatory inspection(s), providing direct access to source data/documents
  67. 67. * *Steps & procedures for monitoring study *Instructions for protocol deviations *Allocation of duties & responsibilities within research teams *Quality control of methods & evaluation procedures
  68. 68. * *Description of how patients/volunteers would be informed
  69. 69. * *Procedures for handling & processing records of effects and adverse events *Handling of Products: * Safe handling and storage measures * System to be followed for labelling * Labeling specifications
  70. 70. * *Budget, financial aspects *Sources of economic support *Subject payments *Reimbursement to team members *Insurance details of study subjects
  71. 71. * Informed Consent
  72. 72. * *Compilation of the clinical and nonclinical data on the investigational product that are relevant to the study of the products in human subjects
  73. 73. * * Introduction Definition Purpose Information form Edition Type & extent Review & revise Up-date * General consideration * Contents of the IB * Conclusion
  74. 74. * ESSENTIAL DOCUMENTS FOR THE CONDUCT OF A CLINICAL TRIAL
  75. 75. * Sec 8: Essential Documents -Introduction *Essential Documents are those documents which individually and collectively permit evaluation of the conduct of a trial and the quality of the data produced. *These documents serve to demonstrate the compliance of the investigator, sponsor and monitor with the standards of Good Clinical Practice and with all applicable regulatory requirements
  76. 76. * Essential Documents to be Kept before Trial Commences Investigators Brochure Signed protocols, amendments (if any) and sample CRF Information given to the trial subjects Informed Consent Applicable translations of informed consent (if any) Any other written information Advertisements for subject recruitment Subject compensation Financial aspects of the trial Compensation document for trial-related injury Signed agreements of all involved parties Investigator and sponsor Investigator and CRO (if any) Investigator/institution and regulatory authorities (if any) Approval letter from the IRB IRB Composition Authorization or notification from the regulatory agencies (where required)
  77. 77. * Essential Documents to be Kept before Trial Commences CV of investigator and sub-investigators evidencing qualifications Normal values of labs /technical procedures included in the protocol Medical/laboratory and technical procedures of tests Certification Accreditation Established Quality control (QC assessments) Other validations Sample labels attached to investigational product containers Instructions for handling investigational products and trial-related materials (sometimes this information is included in the investigator’s brochure) Shipping records of investigational products and trial-related materials Certificates of analysis of investigational products shipped Decoding procedures for blinded trials Master randomization list Pretrial monitoring report Trail initiation monitoring report
  78. 78. * Essential Documents to be Kept During the Trial Investigator’s brochure updates Any revisions to: Protocol, amendments and CRF Informed consent form Written information provided to subjects/LAR Advertisement Dated, IRB approved documents of: Protocol amendments Revisions of informed consent, information to subjects/LAR Advertisements and any other documents given Continuing review of trial Dated Regulatory approved documents of: Authorizations and notifications Protocol amendments and other documents
  79. 79. * Curriculum Vitae of new investigators and sub-investigators Updates to normal value(s) range(s) for medical lab technical procedure(s), test(s) included in the protocol Updates on medical/laboratory/technical procedure tests Certificates Accreditation Established quality control/external quality assessment Other validations Documentation of investigational products and trial-related materials shipment Certificate(s) of analysis for new batches of investigational products Monitoring visit reports Relevant communications other than site visits (Letters, meeting notes and notes of telephone calls) Signed informed consent forms Source documents Signed, dated and completed CRF Documentation of CRF Corrections
  80. 80. * Notification by the originating investigator to sponsor of serious adverse evens and related reports Notification by investigator (if applicable) to regulatory authorities and IRB of unexpected serious adverse reactions and of other safety information Notification by sponsor to investigators of safety information Subject screening log Subject identification code list Subject enrolling log Investigational product(s) accountability at the sire Signature sheet Record of retained body fluids/tissue samples (if any)
  81. 81. * Essential Documents to be Kept After Completion or Termination of the Trial Investigational product(s) accountability at sire Documentation of investigational product(s) destruction Completed subject identification code list (to permit identification of all subjects enrolled in the trial in case of follow up is required – this information should be kept in a confidential manner and for agreed period of time) Audit certificate (if required) Final trial close-out monitoring report Treatment allocation and decoding documentation returned to sponsor to document any decoding that may have occurred Final report by investigator to IRB where required Final report by investigator to regulatory authorities where applicable to document completion of the trial Clinical study report to document results and interpretation
  82. 82. *
  83. 83. * Indian GCP :Dec 2001 Expert Committee set up by Central Drugs Standard Control Organization (CDSCO) in consultation with clinical expert has formulated this GCP guideline • Drug Technical Advisory Board (DTAB), the highest technical body under D&C, Act, has endorsed adoption of this GCP guideline for streamlining the clinical studies in India • These guidelines have been evolved with consideration of WHO, ICH, USFDA and European GCP guidelines as well as the Ethical Guidelines for Biomedical research on Human Subjects issued by the Indian Council of Medical Research. 86
  84. 84. * STRUCTURE ICH E6 * Glossary * Principles * IRB/IEC * Investigator * Sponsor * Protocol * Investigators’ Brochure * Essential Documents Indian GCP * Definitions * Pre-requisites * Responsibilities * Records & Data * Quality Assurance * Statistics * Special Concerns 87 * Appendices
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