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Protocol 02CL2001a Master Informed Consent Form CONFIDENTIAL Wind tree Therapeutics, Inc. Version 2.1, 18 June2021INFORMATION for POTENTIAL PARTICIPANTS Name of Study:A Multi center, SingleTreatment
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01
Read the informed consent form thoroughly to understand the purpose and details of the study or procedure.
02
Provide all necessary personal information such as name, age, contact details, etc.
03
Sign and date the form to indicate your consent to participate or undergo the procedure.
04
Make sure to ask any questions or seek clarification on any doubts before signing the form.

Who needs informed consent form master?

01
Anyone who is participating in a research study or clinical trial that requires informed consent.
02
Patients who are undergoing a medical procedure or treatment that requires their consent.
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The informed consent form master is a document that outlines the details of a study or procedure for a participant to read and sign before agreeing to take part.
Researchers, healthcare providers, or institutions conducting a study or procedure are required to file the informed consent form master.
To fill out the informed consent form master, provide all necessary information about the study or procedure, risks and benefits, and ensure the participant understands before signing.
The purpose of the informed consent form master is to ensure participants are fully informed about a study or procedure, allowing them to make a voluntary and informed decision to participate.
The informed consent form master must include details about the study or procedure, risks and benefits, participant rights, confidentiality measures, and contact information for questions or concerns.
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Relevant keywords

2019 california lucinactant windtree therapeutics 2001a june2021 covid ards irb cov investigational lyophilized tolerability fda sars icf clinicaltrials portability anmat 30th pneumothoraces inflammationrelated californias surfactants inactivated hipaa nd

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