Easily Hide Page Numbers to the Clinical Trial Agreement

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How to Hide Page Numbers to the Clinical Trial Agreement

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hey welcome to House a channel in todays video we will show you how to remove numbering from some pages in Word open the document you need go to layout tab at the top of the window click on breaks under page setup and choose next page scroll down to the next page and click on the footer click on the link to previous in the top of a page delete the number in the footer in our case its 4 you can see the page has number 3 and the next page is without a number put the mouse pointer in the beginning of page 5 and click on page number and choose bottom of page and then plain number 2 you can see the page has numbers again select the page number you need right-click on it and choose format page numbers go to page numbering and check start at 1 and click OK you can see the numbering now begins from the fourth page if you scroll up you can see all above pages have their own numbering thats it thanks for watching the video please like it if you use any of our tips and tricks subscribe to our

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What is the NCT identified number?

ClinicalTrials.gov identifier The unique identification code given to each clinical study upon registration at ClinicalTrials.gov. The format is NCT followed by an 8-digit number (for example, NCT00000419).

Is a clinical trial agreement a contract?

A CTA serves as a legally binding contract between a sponsor, site, and researcher, and outlines each partys responsibilities and obligations for the clinical trial.

What is a unique protocol identification number?

Unique Protocol Identification Number * Definition: Any unique identifier assigned by the sponsor to refer to the availability of its investigational product for expanded access use or to identify the expanded access record. Limit: 30 characters.

What documents should be in a TMF?

Investigator Brochure (IB) and/or Summary of Product Characteristics and any updates. Certificate of Analysis of IMP(s) Instructions for handling the IMP (if not already in the IB) Treatment allocation and decoding documentation (for blinded trials) Drug delivery/return records (e.g. Shipping documents) Sample labels.

What is a protocol number in clinical trials?

The protocol is a document that describes how a clinical trial will be conducted (the objective(s), design, methodology, statistical considerations and organization of a clinical trial,) and ensures the safety of the trial subjects and integrity of the data collected.

Is clinical trial data confidential?

Confidentiality in clinical research in the US is covered by the Privacy Rule that are a set of regulations provided by the department of health and human services (HSS) as a response to a congressional mandate in the Health Insurance Portability and Accountability Act of 1996 (HIPAA).

What are the elements of a clinical trial agreement?

A clinical trials agreement should describe and acknowledge responsibilities, terms of collaboration, requirements for payment and reimbursement, publication and intellectual property terms, indemnification and or insurance, subject injury coverage, guidelines for dispute resolution, grounds for termination of contract

What are the number phases involve in clinical trials?

There are 3 main phases of clinical trials phases 1 to 3. Phase 1 trials are the earliest phase trials and phase 3 are later phase trials. Some trials have an earlier stage called phase 0, and there are some phase 4 trials done after a drug has been licensed.

What is a number attached to each clinical trial protocol?

Registry Identifier: Number assigned by a clinical trial registry (for example, a registry that is part of the World Health Organization [WHO] Registry Network); also required to enter the name of the clinical trial registry.

What aspects of a clinical trial agreement can help protect study volunteers that participate in clinical trials?

Informed consent must be obtained. The consent language agreed to, and the process for obtaining consent, must be carefully documented. Research subject privacy and confidentiality must be adequately protected. The ongoing safety of research subjects must be adequately monitored.

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