Examples of 'notified body shall' in a sentence
Meaning of "notified body shall"
This phrase is commonly used in legal and regulatory contexts, particularly in the European Union (EU) framework. It refers to an organization or body that has been designated and authorized to carry out specific conformity assessment tasks. These tasks may include product certification, testing, inspection, or quality assurance based on applicable EU regulations
How to use "notified body shall" in a sentence
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notified body shall
The report of the notified body shall.
The notified body shall do the following.
In particular the notified body shall.
The notified body shall examine.
An appeal procedure against decisions of the notified body shall be available.
The notified body shall have documented procedures.
The quality management system of the notified body shall address at least the following.
A notified body shall be presumed to meet the harmonised standard.
Independently of the modules chosen by the contracting entity the notified body shall verify that.
And the notified body shall.
Verification by examination and testing of every product The notified body shall.
The notified body shall prior to making a final decision.
During its unexpected visits, the notified body shall.
The notified body shall issue the certificate of conformity of.
Regardless of which module is chosen, the notified body shall check that.
The notified body shall withdraw certificates which are no longer valid.
In relation to surveillance audits of manufacturers, the notified body shall have documented procedures to.
The notified body shall verify the usefulness of the substance.
Notified body quotations and pre-application activities The notified body shall.
The notified body shall provide the manufacturer with a test report.
Surveillance activities and post-certification monitoring The notified body shall have documented procedures.
The notified body shall give the reasons for its decision.
Regardless of which module is chosen, the Notified Body shall verify that.
The notified body shall evaluate the modifications proposed and decide.
If the non-conformity persists the notified body shall inform the notifying Member State.
The notified body shall assess the quality system to determine whether it.
Regardless of whether module CB or CH1 is chosen, the Notified Body shall check that.
The notified body shall transmit the information within a period of one month.
Depending on the categories ( safety level ) a notified body shall be involved.
The notified body shall manage the verification activities and shall in particular.
After its validation, the notified body shall upload the summary to Eudamed.
The notified body shall assess thequality system to determine whetherit satisfies the requirements referred.
If so, the notified body shall inform the manufacturer accordingly.
The notified body shall verify only that the documentation on operation is provided.
If so, the notified body shall inform the installer accordingly.
The notified body shall verify only that the documentation on maintenance is provided.
If so, the notified body shall inform the manufac turer accordingly.
The notified body shall apply a sampling system with the following characteristics.
In such cases, the notified body shall renew the EU type-examination certificate.
The notified body shall notify the manufacturer of its decision to issue the certificate.
The notified body shall not deliver the certificate if that scientific opinion is unfavourable.
The notified body shall take into consideration guidance and best practice documents.
The notified body shall notify its decision to the manufacturer or his authorised representative.
The notified body shall be established under national law and have legal personality.
The notified body shall notify the manufacturer of tits decision to issue the certificate.
The notified body shall periodically carry out audits to make sure that the.
The notified body shall convey its final decision to the medicinal products authority consulted.
The notified body shall document its rationale for the sample or samples of devices taken.
The notified body shall carry out such inspections at least once every three years.
The notified body shall ensure that the manufacturer maintains and applies the approved quality system.
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