logging in or signing up Good Clinical Practices anilmahajan75 Download Post to : URL : Related Presentations : Share Add to Flag Embed Email Send to Blogs and Networks Add to Channel Uploaded from authorPOINT lite Insert YouTube videos in PowerPont slides with aS Desktop Copy embed code: Embed: Flash iPad Dynamic Copy Does not support media & animations Automatically changes to Flash or non-Flash embed WordPress Embed Customize Embed URL: Copy Thumbnail: Copy The presentation is successfully added In Your Favorites. Views: 493 Category: Education License: All Rights Reserved Like it (2) Dislike it (0) Added: July 31, 2012 This Presentation is Public Favorites: 2 Presentation Description GCP Guidelines for Clinical Trial Comments Posting comment... Premium member Presentation Transcript PowerPoint Presentation: 1 Good Clinical Practice Presented By MR. MAHAJAN ANIL J. M.Pharm 2nd Semester Guided By MR. R. SURESH (Asst. Prof.) Sharadchandra Pawar College of Pharmacy, Otur, Pune.Contents : Contents Introduction History Glossary Principles of GCP IEC/IRB Responsibilities Investigator Responsibilities Sponsor Responsibilities Protocols and Amendments Investigator’s Brochure Essential Documents 2PowerPoint Presentation: 3Good Clinical Practice: Good Clinical Practice 4 A Set of Responsibilities ‘a process that makes all parties to a study responsible for patient safety and study quality ’What is GCP ?: What is GCP ? Good Clinical Practice (GCP) is defined as a ‘standard for the design, conduct, performance, monitoring, auditing, recording, analyses and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity and confidentiality of trial subjects are protected’ 5GCP: GCP Are mainly focused on the protection of human rights in clinical trial. Provide assurance of the safety of the newly developed compounds. Provide standards on how clinical trials should be conducted. Define the roles and responsibilities of - Clinical Sponsors, Clinical Research Investigators, Clinical Research Associates, And Monitors. 6The Objectives of Clinical Research: The Objectives of Clinical Research To Contribute to Public Health To Contribute to Health Science To Contribute to Economic Development 7US & EU Objectives in Harmonizing GCP (3 August 2009, Launch of a Bilateral GCP Initiative): US & EU Objectives in Harmonizing GCP (3 August 2009, Launch of a Bilateral GCP Initiative) 8 To achieve common understandings and practices To share standards and methodologies To share knowledge To share resources To improve human subjects protectionsChallenges to GCP Harmonization: Challenges to GCP Harmonization 9 The extensive reach of clinical trials The complexity of law and regulation Lack of an internationally agreed code of ethics for human research protections The progress of medical science The lack of appropriately representative platformsDimensions of GCP: Dimensions of GCP 10 General Frameworks WHO GCP ICH GCP Regional/Applied Frameworks EU GCP US CFR National/Applied GCP Guidelines China, India, Russia, Singapore, Malaysia, Indonesia, South Korea Argentina, Brazil, Mexico, South America, South Africa, TurkeyHistorical perspective: Historical perspective Tuskegee Experiment 1932-1970 Sulphanilamide disaster 1938 Thalidomide Tragedy 1950/60s 11Tuskegee Experiment : Tuskegee Experiment From 1932 -1970 with approval from the US Department of Public Health. Poor black men with syphilis were regularly examined and the progress of their disease documented. The “subjects "believed they were receiving optimal medical treatment. The reality was that either inadequate or no treatment at all was being given. As a direct result of this study at least 40 men lost their lives 12Sulphanilamide disaster 1938: Sulphanilamide disaster 1938 Sulphanilamide widely available and useful antibiotic Manufacturer dissolved the compound in diethylene glycol to make it in elixir. Following acceptable testing for flavour , appearance and fragrance it was distributed. But toxicity profile was not done 1938 –107 deaths (primarily children) directly attributable to the elixir sulphanilamide 13PowerPoint Presentation: 14Thalidomide Tragedy 1950/60s: Thalidomide Tragedy 1950/60s Compound prescribed for nausea in pregnancy throughout Europe No teratogenic testing performed in appropriate animal models Early reports of patients suffering from peripheral neuritis were largely ignored 15PowerPoint Presentation: Estimated 10,000 phocomelics born Despite the evidence the drug manufacturers fought to keep the compound on the market. 16History of Good Clinical Practice: History of Good Clinical Practice Prior to an actual set of guidelines to follow for good clinical practice, clinical studies were dangerous and could result in serous disease, or possibly death. The Nuremburg Code of 1947 Experiments performed in Germany during WWII opened the eyes of the world for guidance for clinical testing on humans. The code did set ethical guidelines, but it lacked legislation to back it up. Declaration of Helsinki In 1964, the World Medical Association established recommendations guiding medical doctors in biomedical research involving human subjects. These guidelines influenced national legislation, but there was no set standard between nations. 17PowerPoint Presentation: 18Glossary: Glossary Adverse drug reaction (ADR) Serious Adverse Event (SAE) Audit Blinding/masking Investigator Protocol Sponsor 1913 Principles of ICH GCP: 13 Principles of ICH GCP Clinical trials should be conducted in accordance with the ethical principles that have their origin in the Declaration of Helsinki, and that are consistent with GCP and the applicable regulatory requirements. Before a trial is initiated, foreseeable risks and inconveniences should be weighed against the anticipated benefit for the individual trial subject & society . A trial should be initiated and continued only if the anticipated benefits justify the risks. Benefits RISKS 2013 Principles of ICH GCP Continued: 13 Principles of ICH GCP Continued The rights, safety, and well-being of the trial subjects are the most important considerations and should prevail over interests of science & society. The available non-clinical & clinical information on an investigational product should be adequate to support the proposed clinical trial. Clinical trials should be scientifically sound, and describe in a clear, detailed protocol. A trial should be conducted in compliance with the protocol that has received prior IRB (or IEC) approval. 2113 Principles of ICH GCP Continued: 13 Principles of ICH GCP Continued The medical care given to, and medical decisions made on behalf of, subjects should always be the responsibility of a qualified physician or, when appropriate, of a qualified dentist. Each individual involved in conducting a trial should be qualified by education, training and experience to perform his or her respective tasks. Freely given informed consent should be obtained from every subject prior to clinical trial participation. 2213 Principles of ICH GCP Continued: 13 Principles of ICH GCP Continued All clinical trial information should be recorded, handled, and stored in a way that allows its accurate reporting, interpretation, and verification. The confidentiality of records that could identify subjects should be protected, respecting the privacy and confidentiality rules in accordance with the applicable regulatory compliance. 2313 Principles of ICH GCP Continued: 13 Principles of ICH GCP Continued 12. Investigational products should be manufactured, handled, and stored in accordance with applicable good manufacturing practice (GMP). They should be used in accordance with the approved protocol 13. Systems with procedures that assure the quality of every aspects of the trial should be implemented. 24Institutional Review Board (IRB), Independent Ethics Committee (IEC): Institutional Review Board (IRB), Independent Ethics Committee (IEC) A formally designated group that oversees research involving human subjects. Approves and disapproves human subject research. According to the standards of the community or the institution, the IRB/IEC may require modifications to a protocol to ensure patient safety. 25IRB Function : IRB Function • The primary function of an IRB/IEC is to safe guard the rights ,safety ,and well being of all trial subjects . This is accomplished by initial, continuing and annual review. •An IRB should consist of members who collectively have the qualifications and experience to review and evaluate the science , medical aspects, and ethics of the proposed trial. 26IRB Members : IRB Members 1. A minimum of five (5) members. 2. One member whose concern is not scientific. 3. One member who has no personal or familial relationship to the institution or trial site. 4. Any member with a conflict of interest may not participate in any part of the review or vote (except to provide requested information). 5. Individuals with special expertise may be invited to assist with areas of unique or complex nature. These will not be voting members. 6. A list of IRB/IEC members and their qualifications should be maintained. 27IRB/Ethics Committee: IRB/Ethics Committee All studies must be approved prior to recruiting participants IRB must review all documents given to participants Reporting AEs and Deviations from protocol to the IRB Maintenance of Records 28Investigator Responsibilities: Investigator Responsibilities Adequate Resources Recruitment Time Qualified Staff Facilities Training 29Investigator Responsibilities: Investigator Responsibilities Medical Care A qualified Physician (or dentist) responsible for trial-related medical decisions Provide adequate medical care for AEs or other significant medical condition Inform SPP about participation in trial Make a reasonable effort to ascertain why participant withdrawals from study 30Investigator Responsibilities: Investigator Responsibilities Compliance with Protocol Investigator should sign off on protocol Investigator should not implement deviations from protocol If deviations occur, they should be documented and reported at once to the sponsor, the IRB and other regulatory authorities 31Investigator Responsibilities: Investigator Responsibilities Progress Reports Written summary of trial status to the IRB Written reports to the sponsor or regulatory authority of any changes affecting the trial Safety Monitoring SAEs should be reported immediately to sponsor AEs should be reported according to sponsor guidelines Supply sponsor & IRB with requested materials on participant deaths 32Investigator Responsibilities: Investigator Responsibilities Premature Termination or Suspension Promptly inform trial subjects Assure appropriate therapy & follow-up to subject Inform sponsor, regulatory authorities & IRB Final Reporting Inform IRB of study completion & a summary of the trial’s outcome Provide sponsor & regulatory authorities with all required reports 33Sponsor Responsibilities: Sponsor Responsibilities Quality Assurance & Quality Control Provide written SOPs Secures agreement between all parties Data handling Contract Research Organization (CRO) Hired by the sponsor to implement trial-related duties Medical Expertise Designated medical personnel to advise on trial-related medical questions and problems 34Sponsor Responsibilities: Sponsor Responsibilities Trial Design Designs of protocol and CRFs Planning analyses to analysing Trial Management, Data Handling, Recordkeeping, & Independent Data Monitoring Committee (DMC) Qualified personnel to supervise overall conduct of the study DMC assesses the progress of the clinical trial Maintain SOPs for electronic data processing Inform Investigator of guidelines for record retention 35Clinical Trial Protocol: Clinical Trial Protocol General Information Background Information Trial Objectives & Purpose Trial Design Selection & Withdrawal of Participants Treatment of Subjects Assessment of Efficacy Assessment of Safety 36Investigator’s Brochure: Investigator’s Brochure Defined as a compilation of the clinical and nonclinical data on the investigational product(s) that are relevant to the study of the product(s) in human subjects. 37Essential Documents for the Conduct of a Clinical Trial: Essential Documents for the Conduct of a Clinical Trial Preclinical trial commencement During clinical conduct of trial After completion or termination of trial 38Storage of Essential Documents : Storage of Essential Documents FDA Rule : 2 options 2 years following marketing of the drug or, 2 years after IND application is withdrawn if drug was not marketed 39References: References http ://www.fda.gov/oc/gcp/guidance.htm http://www.clinicaltrials.gov/ http://www.fda.gov/oc/ohrt/irbs/websites.html http://ohrp.osophs.dhhs.gov/ http://privacyruleandresearch.nih.gov/ http://en.wikipedia.org/wiki/ICH-GCP OECD Principles of Good Laboratory Practice (as revised in 1997)" . OECD Environmental Health and Safety Publications ( OECD ) 1 . 1998. http://www.oecd.org/document/63/0,2340,en_2649_34381_2346175_1_1_1_37465,00.html . 40 References: References Schneider, K (1983(Spring)). "Faking it: The case against Industrial Bio-Test Laboratories" . Amicus Journal (Natural Resources Defence Council): 14-26. http://planetwaves.net/contents/faking_it.html . Tweedale, AC (2011). "Uses of ‘Good Laboratory Practices’ by regulated industry and agencies, and the safety of bisphenol A". J Epidemiol Community Health (BMJ Group) Online First: 15 February 2011 . doi : 10.1136/jech.2010.127761 . . 41PowerPoint Presentation: Thank You 42 You do not have the permission to view this presentation. In order to view it, please contact the author of the presentation.