Committee Registration

The Committee Registration Flow Template is used by Operations departments to accelerate business processes and maintain full control over important documents while eliminating manual actions.

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Implement the Pre-Built Workflow and Enjoy the Benefits of Automation

The automated Committee Registration Flow Template simplifies the work of the operations specialists and helps close important deals without delays or data losses. With easy-to-configure Bots, Operations departments can begin automating on day one, without writing a single line of code.

Check out the benefits airSlate delivers to your team:

  1. Use professional-looking, editable templates.
  2. Set up smart reminders and notifications so you don’t miss deadlines.
  3. Negotiate contracts with your colleagues and partners in real time.
  4. Populate documents and contracts from your data sources using the no-code Bots.
  5. Automatically archive documents to your storage when a task is completed.

Optimize internal processes and focus on critical initiatives with the business automation platform. Deploy it once and save hours of time and hassle on every workflow step.

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Pre-fill Committee Registration fields from a CRM, Spreadsheet or database records

Extract data from Committee Registration to a CRM, Spreadsheet or database

Archive Committee Registration to Google Drive, Dropbox, OneDrive and other cloud storage services

Assign recipients to fields and route the document automatically

Automate repetitive tasks in CRMs, G Suite, and other systems of record

Save an average of 8 hours per week with an automated Committee Registration workflow

Spend an average of 10 minutes to complete a Committee Registration document

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No-code automation, integrations, configuration and distribution of Committee Registration

  • Add additional fillable fields to Committee Registration

    Workflow document feature example Workflow document feature example

  • Embed fillable Committee Registration in your website or distribute it via a public link

    Workflow document feature example Workflow document feature example

  • Collect payments for Committee Registration

    Workflow document feature example Workflow document feature example

  • Authenticate recipients for Committee Registration

    Workflow document feature example Workflow document feature example

  • Request attachments for Committee Registration from recipients

    Workflow document feature example Workflow document feature example

  • Integrate Committee Registration with dynamic web-forms

    Workflow document feature example Workflow document feature example

  • Auto-generate documents from data in Committee Registration

    Workflow document feature example Workflow document feature example
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Configure no-code airSlate Bots in minutes to pre-fill or extract data, integrate into a single or multiple systems of record, automate routing and decisions, or set up reminders, and notifications. Any repetitive task can be done by an existing Bot, or we can build a new one.
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Document generation
The most powerful document generation engine with text tags, fillable fields, e-signature and roles built in, with the ability to connect to multiple data sources simultaneously without writing a single line of code.
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Accept payments
Connect to a payment gateway and accept credit cards, ACH or other forms of payment. Use no-code airSlate Bots to quickly integrate payment collection into contract negotiation, quote-creation, invoicing or accounting.
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Workflow automation
Automate routing, approvals, data collection, reporting and other workflows using no-code airSlate Bots. Configure and deploy them in minutes, no API, coding or complicated standards to learn.
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Contract negotiations
Pre-fill, generate from templates, comment, redline, track changes, approve and e-sign contracts in a single, integrated no-code business automation platform.
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Built-in e-signing
Use airSlate’s enterprise-grade e-signature to set up any multi-signature role-based workflow.
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Mobile-first web forms
Use airSlate’s drag-drop wizard to create powerful, interactive, mobile-native web forms.
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Contract management
Generate quotes, contracts, orders, and invoices while receiving payments and tracking contract execution. Automate every step of the sales and procurement process by integrating with a single platform.
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Advanced analytics
Custom analytics are as easy to set up as our no-code airSlate Bots. Create graphs and reports based on any field in a document, data value, or activity in your workspace.
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Automate multi-step workflows with ready-to-use Bots, from document routing and notifications to generating documents pre-filled with CRM data.
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Go beyond airSlate and make the CRMs and services that you already use a part of your automated workflows. Expand automation to third-party services without the need to code or pay for API integration.

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How to Committee Registration

Watch our quick user guide video and learn how to use the Committee Registration. Our instructions show how to automate, sync, and streamline document workflows without coding.

How to Committee Registration

Hello, friends. Welcome back to the course that is Current Regulatory Requirement for Conducting Clinical Trial for New Drug and Investigational New Drug in India. Up to this we have seen many of the lectures up to lecture 8, and in the lecture 7 and 8 we have seen that the Ethics Committee which is registered with the Central Licensing Authority required to oversee the BA/BE study conduct and the clinical trial study conduct. So, in the lecture that is lecture 9, it is related to the Ethics Committee Registration and Re-registration we are going to see what is means by this exactly Ethics Committee we have referred in our lecture 7 and lecture 8. So, after completion of this lecture the learners will come to know the requirement for Ethics Committee registration; what is Ethics Committee; which Rule s as per New Drug and Clinical Trial are applicable; once it has been registered what is the validity period; then how to apply for Ethics Committee registration at CDSCO that in Central Licensing Authority and whether it is the in the hard copy that is offline or online that will also see. Further, how to apply for the registration and re-registration these things will cover. So, let us start first with what is ethics committee. So, if you recall in our first course, we have given all the schedule wise related Rule s and the 1945 D & C Rule s wherein the definition in the RRule 122 has been given which is related to the ethics committee. As per these definition an Ethics Committee is a committee comprising of medical, scientific, non-medical, non-scientific members whose responsibility is to ensure the protection of the right safety and well being of human subject involved in clinical trial and it shall be responsible for reviewing and approving the protocol, the suitability of the investigators facilities method and adequacy of information to be used for obtaining and documenting informed consent of the study subject and adequacy of confidentiality safeguard. So, this is little bit and the definition of the ethics committee. Now, let us see why it is required to have the Ethics Committee and why its registration is mandatory. So, as per the RRule 6 of New Drug and Clinical Trial Rule , whoever intend to conduct clinical trial or bioavailability study or the bioequivalence study what we have seen in our previous lecture. It shall be required to have approval of an Ethics Committee for clinical trial register under RRule 8. So, in this Rule it has been stipulated that the registered Ethics Committee approval is acceptable. So, the Ethics Committee shall apply for registration with the Central Licensing Authority it is mentioned under Rule 8. Let us see what should be the composition or the constitution of the Ethics Committee for clinical trial Rule . So, dear friends I would like to mention here in this New Drug and Clinical Trial Rule , we have mentioned about two Ethics Committee
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