Fda checklist. 5 Has a quality manager been appointed with defined responsibility This page provides information about the electronic submission of regulatory information to the Center and the review of it by CDER staff. They can be used to verify compliance with the laws administered by the FDA, as a surveillance tool in the wake of outbreaks This guidance discusses De Novo acceptance policies and procedures, Refuse to Accept principles, and the Acceptance Checklist for De Novo Requests. eSTAR provides Jul 17, 2025 · FDA inspection readiness involves preparing for a visit from the U. It requires identifying the specific areas, processes, and departments that will be subject to the audit. txt) or read online for free. Jan 8, 2025 · Keeping track of when, how and why you use medications is important for your health and safety. Does the document file name not contain Download our free FDA BiMo Inspection Checklist Template to ensure thorough preparation, improve compliance, and streamline processes. Guidance documents are prepared for FDA review staff and applicants/sponsors to provide guidelines to the processing, content, and evaluation/approval of applications and also to the design These FDA requirements are described in detail at FDA Strengthens Safety Requirements and Updates Study Results for Breast Implants. Jun 20, 2023 · This checklist explains how to prepare a New Drug Application (NDA) or Biologics License Application (BLA) for submission to the U. Food and Drug Administration The Pre-Approval Inspection Program The Food, Drug, and Cosmetic Act provides that FDA may approve an NDA or an ANDA only if the methods used in, and the facilities and controls used for, the Checklist of Information Usually Submitted in an Investigational Device Exemptions (IDE) Application for Refractive Surgery Lasers [excimer] The FDA inspector will hold an exit interview with the PI at the conclusion of the inspection. Downloadables Public Assistance Information and Receiving Integrated Application Forms and Process In pursuant to FDA Circular No. This checklist is intended as an aid to support clinical decision making for prescribers. The identified predicate(s) is consistent throughout the submission (i. , the predicate(s) identified in the Substantial Equivalence CHECKLIST OF REQUIREMENTS FOR VARIATION AND REVALIDATION OF CERTIFICATE OF PRODUCT REGISTRATION OF A MEDICAL DEVICE CHANGE OF BUSINESS NAME AND ADDRESS OF MANUFACTURER/TRADER/IMPORTER/DISTRIBUTOR This document is an FDA inspection checklist for Acron Mini Drugstore, a super drugstore. Predicate's 51 O(k) number, trade name, and model number (if applicable) provided. 2) of RA 9711 and to the FDA Circular No. The NDA application is the vehicle through which drug sponsors formally Nov 11, 2022 · FDA Inspection The Food and Drug Administration (FDA) conducts inspections and assessments of FDA regulated facilities to determine a firm's compliance with applicable laws and regulations, such as the Food, Drug, and Cosmetic Act and related Acts. Use our checklist to be confident before your next inspection. Updated for 2025. fda. Clinical Trials Guidance DocumentsGuidance documents listed below represent the agency's current thinking on the conduct of clinical trials, good clinical practice and human subject protection The surcharge/penalty for late filing of the renewal of LTO will be assessed pursuant to the Implementing Rules and Regulations (Book II, Article I Section 3. Has the Microsoft Accessibility Checker been run and all Errors or Warnings been remediated? C. The list can be a lifesaver, especially during an emergency. Use SafetyCulture to take Sep 24, 2024 · Learn what an FDA in shipping is, who’s involved, and how automating final disbursement accounts can improve transparency and reduce errors. A. However, use of this checklist is not required to prescribe PAXLOVID. Here are resources to learn more about FDA inspection of cosmetics. Learn key requirements, validation tips, and best practices for regulatory success. See full list on safetyculture. The checklist applies to any SaMD 510 (k) submissions made for medical devices. hhs. With ComplianceQuest, checklists are digitized for easy customization, reuse, and real-time reporting. Master FDA Compliance with this detailed checklist covering classification, QMS, audits, labeling, training, and inspection readiness. Jun 2, 2025 · Download 6 free FDA inspection checklist templates to ensure thorough documentation and improve compliance. 003 Structure of AO Files MDSAP QMS F0015. The document provides guidance for preparing for an FDA audit of a clinical trial. e. It is a version of the checklist we use internally at Innolitics when we’re reviewing 510 (k) submissions for our clients. Mar 28, 2023 · This document provides guidance to the FDA field staff on a new inspectional process that may be used to assess a medical device manufacturer's compliance with the Quality System Regulation and Nov 21, 2024 · The electronic Submission Template And Resource (eSTAR) is an interactive PDF form that guides applicants through the process of preparing a comprehensive medical device submission. ALWAYS BE AUDIT READY Get our FREE 63-Page FDA Inspection Readiness Checklist Included Question Prompts challenge process owners Save time preparing for Mock Inspections Integrate with internal audit program or use informally to uncover compliance problems Sep 23, 2024 · Forms associated with Premarket Notification (510[k]) submissions. May serve as guidelines for effective self-inspection. Please see the attached “Immediate Action Checklist” and institute as soon as a date of audit is determined. Cosmetic establishment instructions, excerpted from FDA's Inspection Operations Manual. Application form is downloaded from www. ph. For predicates that are preamendments devices, information is provided to document preamendments status. Jun 27, 2025 · That’s where the FDA inspection checklist becomes your best defense. com Download Checklist Subscribe to our newsletter and stay updated. Proper preparation including organizing documents and being prepared to answer questions is Food and Drug Administration (FDA) and Occupational Safety and Health Administration (OSHA) Purpose: The Food and Drug Administration (FDA) and the Occupational Safety and Health Administration (OSHA) are providing this checklist for FDA-regulated human and animal food operations to use when assessing operations during the COVID-19 pandemic, especially when re-starting1 operations after a shut This document provides guidance to industry and other stakeholders (e. FDA's Bioresearch Monitoring (BIMO) program is a comprehensive program of on-site inspections and data audits designed to monitor all aspects of the conduct and reporting of FDA regulated research. This page provides information about the electronic submission of regulatory information to the Center and the review of it by CDER staff. gov requirements to accompany certain human drug, biological product and device applications and submissions to FDA. Sep 6, 2024 · This checklist is meant to assist in the review of a 510 (k) submission. Anesthesia machine pre-use check survey: preliminary results. Audit readiness is essential to ensure compliance and success during an FDA inspection for clinical trials. Explore MDSAP audit procedures and forms for harmonized regulatory audits of medical device manufacturers across multiple jurisdictions. Information regarding documenting preamendment status is available online. This webpage provides information about breast implant surgery, including preparing for surgery and postoperative treatment. The scope will help ensure that all relevant aspects are covered, and the audit is comprehensive. Food and Drug Administration. pdf), Text File (. The Revised 508 Standards include Working for nearly two decades as FDA lawyers, we are pleased to provide the following FDA Inspection Checklist to help you complete the needed preparations before the FDA Investigators arrive, to help navigate the process once the inspection has begun, and to appropriately respond to any FDA criticisms once the inspection concludes. The checklist provides details on Regulatory requirements (ISO, FDA, IATF). FDA Lto Checklist - Free download as PDF File (. Sep 23, 2024 · Forms associated with Premarket Notification (510[k]) submissions. Document and record verification. Process adherence and quality control. Oct 17, 2024 · FDA’s Compliance Programs provide instructions to FDA personnel for conducting activities to evaluate industry compliance with the Federal Food, Drug, and Cosmetic Act and other laws First, FDA recommends that the introduction for the checklist include a description of the purpose and importance of the checklist, as well as instructions to patients on how to review and This digital GMP Cosmetics Checklist has been built using the SafetyCulture app and based on the FDA's GMP Cosmetic Guidelines. This guidance is intended to assist institutional review boards (IRBs), clinical investigators, and sponsors in complying with FDA’s informed consent regulations for clinical investigations Inspections are an important part of the FDA’s food safety program. The binder serves as a comprehensive resource for FDA inspectors and helps facilitate the inspection process. PURPOSE This MAPP outlines the policies and procedures for the conduct of a filing review of an abbreviated new drug application (ANDA) by the Division of Filing Review (DFR), Office of Regulatory Oct 21, 2024 · Prepare your biotech company for FDA inspections with our comprehensive checklist. Verify Drug/Device Accountability Check Investigational Product (IP) storage and records. Remco Products presents Food Industry Counsel’s FDA Inspection Checklist as a part of our commitment to bringing our audience the best information in the food industry. Oct 22, 2024 · Suggested Original IDE Application Administrative Checklist Following is a suggested checklist that submitters may use to ensure that their original IDE application is administratively complete. The most recent version is the January 18, 2023 version. Download for a 21 CFR Part 314 Checklist to help understand pharmaceutical regulations the necessary steps for compliance Any “No” answer will result in a “Refuse to Accept” decision; however, FDA staff has discretion to determine whether missing items are needed to ensure that the submission is administratively complete to allow the submission to be accepted or to request missing checklist items interactively from submitters during the RTA review. 2. The FDA inspector will hold an exit interview with the PI at the conclusion of the inspection. Being prepared is not just about documentation—it’s about demonstrating control, traceability, and quality in every process Jun 27, 2018 · Checklist for Evaluating Whether a Clinical Trial or Study is an Applicable Clinical Trial (ACT) Under 42 CFR 11. 1. LASIK Surgery Checklist - Are you a good or poor candidate for Lasik surgery Oct 29, 2022 · In general, FDA inspectors assess current cGMP compliance of the pharmaceutical manufacturing site and issue a detail report. Sample Internal Audit Checklist A sample internal audit checklist offers a starting point for organizations to build tailored 1. Conduct a Mock Audit Simulate an FDA inspection to identify and address potential issues. The draft guidance for industry Drug Master Files describes how to prepare and submit DMFs. To facilitate the development of an ANDA, agency provides the following resources on ANDA forms and In this task, you will prepare the FDA inspection binder, which contains all the necessary documents and information required for the inspection. 001 Checklist of Information to Provide by the Assessment ATL to the APM Checklist of Information Usually Submitted in an Investigational Device Exemptions (IDE) Application for Refractive Surgery Lasers This document is intended to provide guidance in the preparation Dosage Form Drug Manufacturers cGMPs (10/93)GUIDE TO INSPECTIONS OF DOSAGE FORM DRUG MANUFACTURER'S - CGMPR'S Note: This document is reference material for investigators and other FDA personnel Some or all of this checklist may be useful to persons growing, harvesting, packing, manufacturing, processing, or holding human and animal food regulated by FDA. g. Learn essential tips for compliance and how to strengthen your innovation strategy for a positive outcome. Here are some additional resources: Requesting a Pre-Assigned Application Number: To be included in DMF . Key points included: the managing pharmacist was present; required documents for the establishment and pharmacist were Regulatory requirements (ISO, FDA, IATF). This 2025 FDA Audit Survival Guide reveals exactly what inspectors examine, the most common violations, and a step-by-step checklist to ensure compliance. , FDA, NIH, DOD) visit the Human Research Protection Office (HRPO) website's Audit by Federal Agency page. Lampotang S, Moon S, Lizdas DE, Feldman JM, Zhang RV. Oct 17, 2022 · Bioresearch Monitoring Program (BIMO) Compliance ProgramsHome Inspections, Compliance, Enforcement, and Criminal Investigations Compliance Manuals Compliance Program Manual Bioresearch Monitoring A certification of compliance with ClinicalTrials. Food and Drug Administration, which evaluates compliance with regulatory standards for safety, efficacy, and quality in various industries, particularly pharmaceuticals, biotechnology, and food production. What Triggers an FDA Inspection? This supplemental checklist includes study records study teams should review or prepare for an FDA Inspection in addition to documentation listed on Northwestern University IRB’s post-approval monitoring (PAM) checklists. Identify the scope of the FDA audit This task involves determining the extent and focus of the FDA audit. gov. The Food Code represents FDA's best advice for a system of provisions that address the safety and protection of food offered at retail and in food service. Jan 30, 2024 · Here's a step-by-step strategy to achieve compliance with the FDA's updated QMSR regulation. Oct 1, 2020 · Review ChecklistComponents of the checklist: These checklists are a composite of bullet points from (1) regulations, (2) guidance documents, and (3) apheresis device manufacturer directions Jun 5, 2025 · Essential Checklist for Preparing Your Facility for a US FDA Inspection US FDA inspections are a pivotal part of regulatory oversight, determining a pharmaceutical facility’s compliance with Current Good Manufacturing Practices (cGMP) under 21 CFR Parts 210 and 211. That's why a pharmaceutical company should always be inspection ready and in order to facilitate the preparation activities here are a checklist to consider on an ongoing basis: 1. Dec 2, 2024 · FDA Debarment List UpdatesHome Inspections, Compliance, Enforcement, and Criminal Investigations Compliance Actions and Activities FDA Debarment List (Drug Product Applications) FDA Debarment List Oct 1, 2024 · This guidance is intended to describe the Food and Drug Administration's (FDA's) current thinking regarding the scope and application of part 11 of Title 21 of the Code of Federal Regulations This document contains information and guidelines from the U. 4 Have criteria and methods been established to ensure that the operation and control of these processes are effective? 1. Sample Internal Audit Checklist A sample internal audit checklist offers a starting point for organizations to build tailored Although the requirement for a CA for Type II API DMFs is new, FDA has previously evaluated DMFs in accordance with the criteria set out in the GDUFA Completeness Assessment Checklist for Type II The FDA Food Safety Plan Builder (FSPB) is a tool designed to assist owners/operators of food facilities with the development of food safety plans that are specific to their facilities and meet Inspection of Cosmetics FDA has the legal authority to inspect cosmetic establishments as well as cosmetics offered for import. See Attachment 1 to Wipak's 510(k) premarket notification which contains the FDA clearance letter to **Upon notification of FDA audit, immediate steps must be taken in a variety of areas. Ensure GMP compliance, audit readiness, and documentation accuracy. Anesthesiology 1991;75:724-9. A. Describe the specific documents and information you will include in the binder. Preparing for an FDA audit for clinical trials involves proactive planning and adherence to regulatory guidelines. Mar 24, 2021 · HRP-2020 – FDA Site Inspection Preparation Checklist Condensed checklist of recommended steps for the notice of inspection and inspection preparation information FDA Form 483 FAQ page explains its purpose, issuance process, and significance in identifying potential violations during inspections. The escort, PI and any other appropriate staff should attend this interview. The document is a self-assessment toolkit form from the Philippine Department of Health Food and Drug Administration for drugstores, hospital pharmacies, and institutional pharmacies to apply for an initial license to operate. The inspector verified that the drugstore was in compliance with relevant regulations regarding personnel, documentation, premises, equipment, and operations. 22(b) for Clinical Trials Initiated on or After January 18, 20171 (NOT FOR SUBMISSION2) Instructions: Answer the following questions to evaluate whether the study is an applicable clinical trial (ACT). 2014-003: Filing and Receiving of Registration, Licensing and Other Applications Using the Integrated Application Form, the following are the steps of the LTO and CPR ProcessingDownload. The integrated application Mar 28, 2023 · This document provides guidance to the FDA field staff on a new inspectional process that may be used to assess a medical device manufacturer's compliance with the Quality System Regulation and CHECKLIST OF REQUIREMENTS FOR VARIATION AND REVALIDATION OF CERTIFICATE OF PRODUCT REGISTRATION OF A MEDICAL DEVICE CHANGE OF BUSINESS NAME AND ADDRESS OF MANUFACTURER/TRADER/IMPORTER/DISTRIBUTOR The Food Defense Plan Builder is a user-friendly software program designed to assist owners and operators of food facilities develop personalized food defense plans for their facilities. txt) or view presentation slides online. **Upon notification of FDA audit, immediate steps must be taken in a variety of areas. Jan 6, 2025 · Guidance for Industry and Rules related to the FDA Food Safety Modernization Act. , consumer interest groups, academia, other regulatory groups) on FDA’s current thinking concerning what constitutes Good Sep 6, 2023 · These inspections ensure that sites consistently manufacture drug products of acceptable quality and minimize patient and consumer exposure to adulterated drug products. Access a detailed step-by-step checklist to embed complete compliance with the FDA's requirements for electronic record and signature management laid out in 21 CFR Part 11. The inspection checklist summarizes the inspection of Sardam Drugstore in Brgy. “CGMP data Foreword This document provides guidance to the FDA field staff on a new inspectional process that may be used to assess a medical device manufacturer’s compliance with the Quality System Accessed March 13, 2008 March MG, Crowley JJ. Mar 26, 2025 · The FDA aspires to assist applicants in developing abbreviated new drug applications (ANDAs). Pre-Approval Inspection (PAI) Program and How to prepare for a successful outcome Denise DiGIulio Reviewer Process and Facilities CDER/Office of Pharmaceutical Quality Apr 22, 2024 · PMA Review Checklist The checklist referenced below is used by PMA reviewers to determine the completeness of a PMA and is a part of the Blue Book Memo, PMA Refuse to File Procedures 5/2/94 (P94-1). Corrective and preventive action (CAPA) tracking. S. 2011-004 as follows: “An application for renewal of an LTO received after its date of expiration shall be subject to a surcharge or penalty equivalent to twice the renewal licensing fee and an Nov 11, 2024 · Your warehouse FDA inspection checklist should include items like lighting conditions, storage racks, important structural components, and fire safety systems. A letter may be sent to the PI requesting certain documents be copied and ready for the inspection. Obtaining regular and thorough inspections can help you boost safety in your warehouse and reduce operational costs. The De Novo process provides a pathway to classify novel medical devices for which general controls alone, or general and special controls, provide reasonable assurance of safety and effectiveness FDA invites individuals to report suspected data integrity issues that may affect the safety, identity, strength, quality, or purity of drug products at DrugInfo@fda. Jan 19, 2024 · MDSAP QMS P0015. Has the Document Inspector been run on the document? B. For decades, the regulation and control of new drugs in the United States has been based on the New Drug Application (NDA). 20 Paratong, Paoay, Ilocos Norte. The guidance includes acceptance checklists for each type of 510 (k) submission: Jan 5, 2025 · Prepare for FDA inspections with expert tips on maintaining documentation, ensuring personnel readiness, and implementing robust quality systems for seamless compliance and operational excellence. Perfect for any industry. The version date is displayed in the top left corner of page i. Use the accompanying "Elaboration" for additional information to help answer the FDA Pre-Inspection Checklist Organizational tool to aid inspection preparation FDA Inspection Information Intake form for FDA/OHRP Inspection Requests UCSF Guidance for Departments Customizable template that outlines the process for an FDA/OHRP inspection, and describes activities that should be done to facilitate the inspection Download the FDA Inspection Readiness Checklist Use our checklist to: Evaluate documentation, training, and compliance systems Identify risks and implement preventive actions Get your inspection team prepared ahead of time Download the FDA Inspection Checklist on FDA Tracker and move toward a smarter, more resilient inspection readiness strategy. The guidance includes a Written Procedures Checklist (also referred to in this guidance as the Checklist) that incorporates the HHS and FDA regulatory requirements for written procedures for the Pharmaceutical Quality Control Labs (7/93)GUIDE TO INSPECTIONS OF PHARMACEUTICAL QUALITY CONTROL LABORATORIES Note: This document is reference material for investigators and other FDA personnel Microbiological Pharmaceutical Quality Control Labs (7/93)GUIDE TO INSPECTIONS OF MICROBIOLOGICAL PHARMACEUTICAL QUALITY CONTROL LABORATORIES Note: This document is reference material for Checklist for Setting up a WebTrader Account for the FDA Electronic Submissions Gateway (ESG) For assistance with ESG related items, please contact ESGHelpDesk@fda. Make sure there are two copies of every document (one for the investigator/one for the CTO records). This CGMP checklist is based on the Code of Federal Regulations, Title 21, Part 117 (Current Good Manufacturing Practice, Hazard The Food Defense Plan Builder is a user-friendly software program designed to assist owners and operators of food facilities develop personalized food defense plans for their facilities. The desired result is Dec 6, 2024 · Food Code 2022Originally posted December 28, 2022. This detailed guide explores what the FDA looks for, how to prepare, and what steps to take to remain inspection-ready. The process we outline is applicable to all devices reviewed in a PMA application and has been compiled into a checklist for use by FDA review staff. Guidance documents are prepared for FDA review staff and applicants/sponsors to provide guidelines to the processing, content, and evaluation/approval of applications and also to the design The process we outline is applicable to all devices reviewed in a PMA application and has been compiled into a checklist for use by FDA review staff. Feb 22, 2022 · Learn more about why and how the FDA regulates pharmaceuticals, and how the approval process works. Although there are countless variables which will ultimately afect the way in which your next FDA inspection unfolds, the information provided within this FDA Inspection Checklist is designed to provide some of the tools you will need to deal with the most common scenarios. Confirm documentation of receipt, dispensing, and return/destruction. An evaluation of anesthesiologists’ present checkout methods and the validity of the FDA checklist. As a thank you we’ll send you a link to download the FREE checklist! May 23, 2024 · When you’re being audited or inspected by the FDA, you must be ready for anything. (abstract) Anesthesiology 2005;103 (Suppl):A1195. National Center for Complementary and Integrative Health Research Toolbox FDA Inspection Tools FDA Inspection - Guidance FDA Inspection - Checklist For guidance on audits or inspections being conducted by federal regulatory agencies (e. Wipak's Steriking products and See and Peel products are already the subject of an FDA-cleared 5 I0(k) premarket notification; on September 26, 1994 FDA sent a substantial equivalence letter covering these products to Gainor Medical, a distributor of Wipak's sterilization wraps and packs. Download Resource Following Current Good Manufacturing Practices (CGMP) is, in general, required if you manufacture, process, pack or hold human food. 5 Has a quality manager been appointed with defined responsibility PURPOSE This MAPP outlines the policies and procedures for the conduct of a filing review of an abbreviated new drug application (ANDA) by the Division of Filing Review (DFR), Office of Regulatory FDA-BIMO-Checklist - Free download as PDF File (. It contains 13 items that will be checked by FDA inspectors during their visit, including verifying the drugstore's business registration, credentials of pharmacists and assistants, risk management plans, storage procedures, prescription records, and reference materials. 004 Naming Convention of Electronic Record Policy MDSAP QMS F0015. The U. Developing a comprehensive FDA audit checklist for clinical trials helps streamline processes, ensuring proper documentation, data integrity, and protocol adherence. Even if not required, if you sell food to the public, using this guidance will support the production of safer food. May 22, 2025 · Get your biotech or pharma company ready for FDA inspections with this expert-crafted checklist. The Food Code is a model Aug 4, 2022 · FDA's Bioresearch Monitoring (BIMO) program is a comprehensive program of on-site inspections, data audits, and remote regulatory assessments designed to monitor all aspects of the conduct and 2 FDA’s authority for CGMP comes from FD&C Act section 501(a)(2)(B), which states that a drug shall be deemed adulterated if “the methods used in, or the facilities or controls used for, its Mar 31, 2022 · IND Forms and InstructionsHome Drugs Development & Approval Process | Drugs How Drugs are Developed and Approved Types of Applications Investigational New Drug (IND) Application IND Forms and Pre-Approval Inspection (PAI) Program and How to prepare for a successful outcome Denise DiGIulio Reviewer Process and Facilities CDER/Office of Pharmaceutical Quality May 7, 2025 · Ensure FDA compliance with 21 CFR Part 11 for electronic records & signatures in pharmaceuticals, biotech, and medical devices. FDA inspections cover following sectors - vaccine and drug manufacturers blood banks food processing facilities dairy farms animal feed processors Accessibility Guidance and Checklists Federal agencies are responsible for ensuring their information and services are accessible to persons with disabilities. Use this digital GMP checklist to assess your manufacturing compliance with FDA guidelines across aspects of building and facilities, equipment, personnel, raw materials, production, lab controls, record keeping, labelling and complaints. Feb 15, 2022 · Forms & Submission Requirements and applicationsForms Official FDA applications and submissions forms Electronic Regulatory Submission and Review Information about review and electronic submission Apr 17, 2024 · A blog about pharmaceutical quality control, quality assurance, microbiology, production and regulatory updates provided by regulatory agencies. Dec 5, 2024 · FDA’s drug application approval includes assessing the manufacturing process and the facility, including information the agency gained through inspections or alternative tools, to ensure the The guide was prepared by the Food and Drug Administration (FDA) Office of Regula-tory Affairs (ORA), and the Center for Devices and Radio-logical Health (CDRH). This guidance establishes procedures for determining PMA acceptance and filing reviews to make a threshold determination about whether an application is administratively complete for the Agency to Oct 21, 2024 · The FDA conducts careful inspections of facilities that perform nonclinical laboratory studies to determine compliance with Part 58 (Good Laboratory Practice for Nonclinical Laboratory Studies) of 1. Food and Drug Administration (FDA) participates in the Medical Device Single Audit Program, which impacts how the Quality System Inspection Technique (QSIT) is implemented in routine and non-routine inspections. It outlines regulations and responsibilities, documents needed for the audit, and questions the auditor may ask. The NDA application is the vehicle through which drug sponsors formally A certification of compliance with ClinicalTrials. bsswp rjcqnff mzcwjuv qfeje fgywkz qjlfib aqij tvg ctockpl dsvt