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CONTRACT FOR CONDUCTING CLINICAL INVESTIGATION ON A MEDICAL DEVICE NOT EC MARKED OR EC MARKED BUT USED OUTSIDE THE SCOPE OF ITS INTENDED USE [Name of medical device] CLINICAL INVESTIGATION ___BETWEEN
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01
Review the terms and conditions of the contract.
02
Fill out all necessary information accurately, including names, signatures, dates, and contact information.
03
Specify the scope of work to be performed during the clinical trial.
04
Include payment terms and any additional fees or expenses that may be incurred.
05
Include confidentiality agreements to protect sensitive information.
06
Consult legal counsel if needed to ensure the contract is legally binding.

Who needs contract for conducting clinical?

01
Medical research institutions conducting clinical trials.
02
Pharmaceutical companies sponsoring clinical trials.
03
Contract research organizations coordinating clinical trials.
04
Healthcare providers participating in clinical trials.
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Contract for conducting clinical is a legal agreement between a sponsor and a clinical investigator or institution, outlining the terms and conditions of a clinical trial.
The sponsor or the party funding the clinical trial is required to file the contract for conducting clinical.
The contract can be filled out by including all necessary terms, conditions, and agreements related to the clinical trial, and signed by both parties involved.
The purpose of the contract is to establish clear guidelines and responsibilities for both the sponsor and the clinical investigator or institution conducting the trial.
The contract must include details such as the protocol of the clinical trial, responsibilities of each party, financial terms, and any legal obligations.
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2017 2016 undertakes gdpr eur organisational multicentre ecrf seq investigational nhs iib iia crf evaluable indicatively anonymised cumulatively investigation1 verifications conciliate sistema lawfulness interscambio centralised prodromal homogeneity etic

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