Change date in the protocol

Aug 6th, 2022
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Change date in protocol quickly with a all-encompassing online editor

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DocHub provides a effortless and user-friendly solution to change date in your protocol. Regardless of the characteristics and format of your form, DocHub has everything you need to ensure a simple and hassle-free modifying experience. Unlike similar tools, DocHub stands out for its exceptional robustness and user-friendliness.

DocHub is a web-centered tool allowing you to tweak your protocol from the convenience of your browser without needing software downloads. Owing to its simple drag and drop editor, the option to change date in your protocol is fast and simple. With rich integration options, DocHub allows you to transfer, export, and alter documents from your selected platform. Your updated form will be saved in the cloud so you can access it readily and keep it safe. Additionally, you can download it to your hard drive or share it with others with a few clicks. Also, you can transform your file into a template that prevents you from repeating the same edits, such as the ability to change date in your protocol.

How can I use DocHub to quickly change date in protocol?

  1. Import your form to DocHub’s editor by clicking ADD NEW > Select From Device.
  2. Then open your form and use our main toolbar to find and utilize the option to change date in your protocol.
  3. Make the most of other editing and annotating features available in our editor to improve the file’s quality.
  4. When completed, hit Done, then choose Save As to download your protocol or pick another export method.

Your edited form will be available in the MY DOCS folder inside your DocHub account. Moreover, you can utilize our editor panel on the right to combine, split, and convert files and rearrange pages within your documents.

DocHub simplifies your form workflow by providing an incorporated solution!

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How to change date in the protocol

5 out of 5
46 votes

In this video tutorial, the speaker addresses a technical question regarding protocol deviations posed by someone in data management. They emphasize the importance of experience at a research site for professionals in the industry, suggesting that such experience provides practical insights that can clarify confusing aspects of the job. The speaker expresses frustration with mandates but advocates for the value of site experience, which helps individuals understand field specifics in databases and protocol deviations, particularly the differences in dates related to these deviations. This foundational knowledge can prevent confusion and improve industry understanding.

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Here are some common questions from our customers that may provide you with the answer you're looking for. If you can't find an answer to your question, please don't hesitate to reach out to us.
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A sponsor shall submit a protocol amendment for a new protocol or a change in protocol before its implementation. Protocol amendments to add a new investigator or to provide additional information about investigators may be grouped and submitted at 30-day intervals.
A sponsor shall submit a protocol amendment when a new investigator is added to carry out a previously submitted protocol, except that a protocol amendment is not required when a licensed practitioner is added in the case of a treatment protocol under 312.315 or 312.320.
Any docHub change in the design of a protocol (such as the addition or elimination of a control group). Addition of a new test or procedure intended to improve monitoring for, or reduce the risk of, a side effect or adverse event; or elimination of a test intended to monitor safety.
A protocol amendment is a written description of a change to or formal clarification to some aspect of the study that is described in the protocol.
Any modifications to the protocol which may impact on the conduct of the study, potential benefit of the patient or may affect patient safety, including changes of study objectives, study design, patient population, sample sizes, study procedures, or docHub administrative aspects will require a formal amendment to
Sponsors are responsible for selecting qualified investigators, providing them with the information they need to conduct an investigation properly, ensuring proper monitoring of the investigation(s), ensuring that the investigation(s) is conducted in ance with the general investigational plan and protocols
Sponsors are responsible for selecting qualified investigators and providing them with the information they need to conduct the investigation properly, ensuring proper monitoring of the investigation, ensuring that IRB review and approval are obtained, submitting an IDE application to FDA, and ensuring that any
The median direct cost to implement a substantial amendment was US$141,000 for a phase II protocol and $535,000 for a phase III protocol.

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