{"id":32746,"date":"2023-10-19T05:07:35","date_gmt":"2023-10-19T05:07:35","guid":{"rendered":"https:\/\/www.process.st\/templates\/fda-ind-process\/"},"modified":"2024-03-05T14:41:39","modified_gmt":"2024-03-05T14:41:39","slug":"fda-ind-process","status":"publish","type":"post","link":"https:\/\/www.process.st\/templates\/fda-ind-process\/","title":{"rendered":"FDA IND Process"},"content":{"rendered":"\n<section id=\"identify-the-drug-to-be-tested\"> \n <h2>Identify the drug to be tested<\/h2>\n <div class=\"text-content\">\n   This task is the first step in the FDA IND process. Here, you need to identify the drug that will be tested. Consider factors such as the purpose of the drug, potential benefits, and previous research. Once identified, the drug will be used throughout the entire process as the focus of testing. \n <\/div> \n <div class=\"text-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Drug name <\/label> \n   <input type=\"text\" placeholder=\"Something will be typed here...\" disabled class=\"form-control\"> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"complete-preclinical-testing\"> \n <h2>Complete preclinical testing<\/h2>\n <div class=\"text-content\">\n   Preclinical testing is crucial to determine the safety and effectiveness of the drug before it can be tested on humans. This task involves conducting various experiments and studies on animals or in vitro models. Preclinical testing will provide valuable data to evaluate the drug's potential and identify any potential risks or side effects. \n <\/div> \n <div class=\"multi-choice-content form-field-content\"> \n  <div class=\"form-group\"> <label> Preclinical testing methods <\/label> <select disabled class=\"form-control\"> <option value=\"\">Multiple options can be selected from this list<\/option> <\/select> \n  <\/div> \n  <ul class=\"items\"> \n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       1 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Animal studies \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       2 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      In vitro studies \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       3 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Pharmacokinetics analysis \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       4 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Toxicology analysis \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       5 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Dosage determination \n    <\/div> <\/li> \n  <\/ul> \n <\/div> \n<\/section> \n<section id=\"gather-data-from-testing\"> \n <h2>Gather data from testing<\/h2>\n <div class=\"text-content\">\n   In this task, you will gather and collect the data obtained from the preclinical testing phase. This data includes results from different experiments, measurements, observations, and analyses. Ensure that all relevant data is compiled and organized accurately for further analysis and reporting. \n <\/div> \n <div class=\"file-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Upload preclinical testing data <\/label> \n   <div class=\"file-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-upload btn-icon\"><\/i> File will be uploaded here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"approval-preclinical-testing-data\"> \n <h2>Approval: Preclinical Testing Data<\/h2>\n <div class=\"approval-content\"> \n  <div class=\"header\"> \n   <div class=\"list-title\">\n    Will be submitted for approval:\n   <\/div> \n  <\/div> \n  <div class=\"approval-rule-subject-tasks-list\"> \n   <ul class=\"list\"> \n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Complete preclinical testing<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li> \n   <\/ul> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"draft-investigational-new-drug-ind-application\"> \n <h2>Draft Investigational New Drug (IND) application<\/h2>\n <div class=\"text-content\">\n   The IND application is a comprehensive document that provides detailed information about the drug, its composition, preclinical testing data, manufacturing process, proposed clinical trials, and safety assessments. This task requires drafting a well-written IND application that meets the FDA's guidelines and includes all necessary information. \n <\/div> \n <div class=\"textarea-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Draft IND application <\/label> <textarea placeholder=\"Something will be typed here...\" rows=\"3\" disabled class=\"form-control\"><\/textarea> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"compile-manufacturing-information\"> \n <h2>Compile manufacturing information<\/h2>\n <div class=\"text-content\">\n   This task involves gathering information about the manufacturing process and facilities where the drug will be produced. The manufacturing information should include details about the equipment, quality control measures, personnel, and compliance with Good Manufacturing Practices (GMP). Compile all the necessary information to ensure that the drug is manufactured consistently and meets quality standards. \n <\/div> \n <div class=\"text-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Manufacturer name <\/label> \n   <input type=\"text\" placeholder=\"Something will be typed here...\" disabled class=\"form-control\"> \n  <\/div> \n <\/div> \n <div class=\"text-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Manufacturing facilities location <\/label> \n   <input type=\"text\" placeholder=\"Something will be typed here...\" disabled class=\"form-control\"> \n  <\/div> \n <\/div> \n <div class=\"multi-choice-content form-field-content\"> \n  <div class=\"form-group\"> <label> Manufacturing quality standards <\/label> <select disabled class=\"form-control\"> <option value=\"\">Multiple options can be selected from this list<\/option> <\/select> \n  <\/div> \n  <ul class=\"items\"> \n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       1 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      GMP \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       2 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      ISO 9001 \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       3 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      ISO 13485 \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       4 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Other \n    <\/div> <\/li> \n  <\/ul> \n <\/div> \n<\/section> \n<section id=\"include-data-from-preclinical-tests\"> \n <h2>Include data from preclinical tests<\/h2>\n <div class=\"text-content\">\n   In this task, you will integrate the data from the preclinical testing phase into the IND application. The data should be presented in a clear and concise manner, highlighting the key findings and supporting evidence. Ensure that the data is properly referenced and accurately represents the outcomes of the preclinical tests. \n <\/div> \n <div class=\"file-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Upload preclinical test data for IND application <\/label> \n   <div class=\"file-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-upload btn-icon\"><\/i> File will be uploaded here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"outline-proposed-clinical-trials\"> \n <h2>Outline proposed clinical trials<\/h2>\n <div class=\"text-content\">\n   This task involves outlining the design and objectives of the proposed clinical trials for the investigational drug. Consider factors such as the number of participants, inclusion and exclusion criteria, trial duration, and endpoints. Provide a clear and comprehensive outline that demonstrates a well-planned and scientifically rigorous approach for the clinical trials. \n <\/div> \n <div class=\"textarea-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Outline proposed clinical trials <\/label> <textarea placeholder=\"Something will be typed here...\" rows=\"3\" disabled class=\"form-control\"><\/textarea> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"approval-clinical-trials-proposal\"> \n <h2>Approval: Clinical Trials Proposal<\/h2>\n <div class=\"approval-content\"> \n  <div class=\"header\"> \n   <div class=\"list-title\">\n    Will be submitted for approval:\n   <\/div> \n  <\/div> \n  <div class=\"approval-rule-subject-tasks-list\"> \n   <ul class=\"list\"> \n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Draft Investigational New Drug (IND) application<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li>\n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Compile manufacturing information<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li>\n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Outline proposed clinical trials<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li> \n   <\/ul> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"submit-completed-ind-application-to-fda\"> \n <h2>Submit completed IND application to FDA<\/h2>\n <div class=\"text-content\">\n   Once the IND application is complete, it needs to be submitted to the FDA for review. This task involves preparing the necessary documents, double-checking the application for completeness and accuracy, and following the FDA's submission guidelines. Ensure that all required forms, signatures, and supporting documents are included before submitting the application. \n <\/div> \n <div class=\"text-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Submission ID <\/label> \n   <input type=\"text\" placeholder=\"Something will be typed here...\" disabled class=\"form-control\"> \n  <\/div> \n <\/div> \n <div class=\"date-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Submission date <\/label> \n   <div class=\"date-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-calendar btn-icon\"><\/i> Date will be set here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n <div class=\"file-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Upload completed IND application <\/label> \n   <div class=\"file-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-upload btn-icon\"><\/i> File will be uploaded here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"wait-for-fda-review\"> \n <h2>Wait for FDA review<\/h2>\n <div class=\"text-content\">\n   After submitting the IND application, it undergoes a review process by the FDA. This task requires patience and anticipation as the FDA reviews the application for its scientific validity, safety, and ethical considerations. The FDA may request additional information or clarification during the review period, requiring prompt response and cooperation. \n <\/div> \n <div class=\"date-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Expected FDA review completion date <\/label> \n   <div class=\"date-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-calendar btn-icon\"><\/i> Date will be set here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"begin-adaptive-phase-i-trials-after-30day-waiting-period\"> \n <h2>Begin Adaptive Phase I Trials after 30-day waiting period<\/h2>\n <div class=\"text-content\">\n   Once the FDA review is completed and the IND application is approved, the Adaptive Phase I Trials can commence. This task marks the beginning of the clinical trials on human subjects. Ensure that the 30-day waiting period is adhered to, and all necessary preparations for the trials, such as recruitment of participants and establishment of trial sites, are in place. \n <\/div> \n <div class=\"date-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Adaptive Phase I Trials start date <\/label> \n   <div class=\"date-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-calendar btn-icon\"><\/i> Date will be set here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"track-and-record-trial-results\"> \n <h2>Track and Record Trial Results<\/h2>\n <div class=\"text-content\">\n   During the Adaptive Phase I Trials, it is essential to track and record the results meticulously. This task involves the collection and analysis of data obtained from participants during the trials. Track relevant parameters, adverse events, and any other observations that can contribute to evaluating the safety and efficacy of the investigational drug. \n <\/div> \n <div class=\"file-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Upload trial results <\/label> \n   <div class=\"file-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-upload btn-icon\"><\/i> File will be uploaded here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"approval-phase-i-trial-results\"> \n <h2>Approval: Phase I Trial Results<\/h2>\n <div class=\"approval-content\"> \n  <div class=\"header\"> \n   <div class=\"list-title\">\n    Will be submitted for approval:\n   <\/div> \n  <\/div> \n  <div class=\"approval-rule-subject-tasks-list\"> \n   <ul class=\"list\"> \n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Begin Adaptive Phase I Trials after 30-day waiting period<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li>\n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Track and Record Trial Results<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li> \n   <\/ul> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"begin-phase-ii-trials\"> \n <h2>Begin Phase II Trials<\/h2>\n <div class=\"text-content\">\n   Upon successful completion of Adaptive Phase I Trials, the Phase II Trials can commence. This task marks the initiation of the next stage of clinical testing. Ensure that the protocols and procedures defined for the Phase II Trials are followed meticulously. Monitor and evaluate the participants' responses to the drug, collect data, and track adverse events to continue assessing its safety and efficacy. \n <\/div> \n <div class=\"date-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Phase II Trials start date <\/label> \n   <div class=\"date-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-calendar btn-icon\"><\/i> Date will be set here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"monitor-and-record-trials\"> \n <h2>Monitor and Record Trials<\/h2>\n <div class=\"text-content\">\n   Throughout the clinical trials, it is crucial to monitor the participants closely and record any relevant changes or outcomes. This task involves regular check-ins, assessments, and data collection to ensure the ongoing safety and effectiveness evaluation of the investigational drug. Employ appropriate monitoring techniques and tools to collect accurate and reliable data. \n <\/div> \n <div class=\"multi-select-content form-field-content\"> \n  <div class=\"form-group\"> <label> Monitor and record trials <\/label> \n  <\/div> \n  <ul class=\"items\"> \n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       1 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Check participant vitals \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       2 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Administer drug doses \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       3 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Collect participant feedback \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       4 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Document adverse events \n    <\/div> <\/li>\n   <li class=\"item\"> \n    <div class=\"step-number-container\"> \n     <div class=\"step-number\">\n       5 \n     <\/div> \n    <\/div> \n    <div class=\"step-checkbox-container\"> \n     <div class=\"step-checkbox\"><\/div> \n    <\/div> \n    <div class=\"item-name-static\">\n      Record data \n    <\/div> <\/li> \n  <\/ul> \n <\/div> \n<\/section> \n<section id=\"approval-phase-ii-trial-results\"> \n <h2>Approval: Phase II Trial Results<\/h2>\n <div class=\"approval-content\"> \n  <div class=\"header\"> \n   <div class=\"list-title\">\n    Will be submitted for approval:\n   <\/div> \n  <\/div> \n  <div class=\"approval-rule-subject-tasks-list\"> \n   <ul class=\"list\"> \n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Begin Phase II Trials<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li>\n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Monitor and Record Trials<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li> \n   <\/ul> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"start-phase-iii-trials\"> \n <h2>Start Phase III Trials<\/h2>\n <div class=\"text-content\">\n   Upon successful completion of Phase II Trials and obtaining promising results, Phase III Trials can be initiated. This task marks the final stage of clinical testing before the drug can be approved by the FDA. Develop comprehensive trial protocols, recruit participants, and ensure adherence to guidelines and regulations. Monitor the participants closely and gather substantial data to evaluate the drug's overall effectiveness and safety. \n <\/div> \n <div class=\"textarea-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Phase III Trials protocols <\/label> <textarea placeholder=\"Something will be typed here...\" rows=\"3\" disabled class=\"form-control\"><\/textarea> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"compile-and-submit-trial-results\"> \n <h2>Compile and Submit Trial Results<\/h2>\n <div class=\"text-content\">\n   At the end of the Phase III Trials, it is essential to compile all the trial results into a comprehensive report. This task involves analyzing and summarizing the data collected throughout the trials, including efficacy, safety, and any observed adverse events. Compile the trial results accurately and submit them to the FDA for review and consideration in the final drug approval process. \n <\/div> \n <div class=\"file-field-content form-field-content\"> \n  <div class=\"form-group\"> <label> Upload trial results report <\/label> \n   <div class=\"file-container\"> <button type=\"button\" disabled class=\"btn btn-default\"> <i class=\"fa fa-upload btn-icon\"><\/i> File will be uploaded here <\/button> \n   <\/div> \n  <\/div> \n <\/div> \n<\/section> \n<section id=\"approval-final-submission-of-trial-results\"> \n <h2>Approval: Final Submission of Trial Results<\/h2>\n <div class=\"approval-content\"> \n  <div class=\"header\"> \n   <div class=\"list-title\">\n    Will be submitted for approval:\n   <\/div> \n  <\/div> \n  <div class=\"approval-rule-subject-tasks-list\"> \n   <ul class=\"list\"> \n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Start Phase III Trials<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li>\n    <li> \n     <div class=\"approval-rule-subject-tasks-list-item\"> \n      <div class=\"item\"> \n       <div class=\"container\"> <span class=\"title\">Compile and Submit Trial Results<\/span> \n        <div class=\"body\">\n         Will be submitted\n        <\/div> \n       <\/div> \n      <\/div> \n     <\/div> <\/li> \n   <\/ul> \n  <\/div> \n <\/div> \n<\/section>\n","protected":false},"excerpt":{"rendered":"<p>Identify the drug to be tested This task is the first step in the FDA IND process. Here, you need to identify the drug that will be tested. Consider factors such as the purpose of the drug, potential benefits, and previous research. Once identified, the drug will be used throughout the entire process as the [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"ep_exclude_from_search":false,"cover_icon_emoji":"\ud83d\udd2c","cover_icon_url":"","tasks_count":"20","template_description":"","template_id":"mbSlIlo2qEDLUqChgD5I4A","task_0":"Identify the drug to be tested","task_slug_0":"identify-the-drug-to-be-tested","task_1":"Complete preclinical testing","task_slug_1":"complete-preclinical-testing","task_2":"Gather data from testing","task_slug_2":"gather-data-from-testing","task_3":"Approval: Preclinical Testing Data","task_slug_3":"approval-preclinical-testing-data","task_4":"Draft Investigational New Drug (IND) application","task_slug_4":"draft-investigational-new-drug-ind-application","task_5":"Compile manufacturing 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