Some examples and use cases from the internet:

Some examples and use cases from the internet:

• implanted medical devices.
• I can get you medical records, deployment documentation.
• If an applicant for an LAPL medical certificate is referred to an AME or AeMC in accordance with MED.B.001, the GMP shall transfer the relevant medical documentation to the AeMC or AME.
• If an applicant for a Class 1 or Class 2 medical certificate is referred to the licensing authority in accordance with MED. B.001, the AeMC or AME shall transfer the relevant medical documentation to the licensing authority.
• There was nothing unusual in this, and it is backed up by the appropriate medical documentation.
• As you know, the FDA requires fastidious documentation of any surgically
• the medical assessor or medical staff designated by the competent authority shall evaluate the relevant medical documentation and request further medical documentation, examinations and tests where necessary; and
• 'electronic health record' means a comprehensive medical record or similar documentation of the past and present physical and mental state of health of an individual in electronic form, and providing for ready availability of these data for medical treatment and other closely related purposes;

• The Marketing Authorisation Holder should provide all supporting data (preclinical and clinical documentation, including the expert reports, efficacy and tolerance studies conducted), to justify a positive benefit
• Following the opinion on the quality data, the marketing authorisation holder, where requested by the Agency, shall submit the clinical documentation and data concerning stability of the medicinal product to the Agency by day 57 at the latest.
• clinical and clinical documentation must be sufficiently detailed to enable an objective judgement to be made.
• The reference Member State will circulate the assessment report on the clinical documentation with its final decision to the concerned Member States within seven days from receipt of the clinical data.
• The dossier on efficacy shall include all pre
• clinical and clinical documentation and/or results of trials, whether favourable or unfavourable to the veterinary medicinal products, in order to enable an objective overall assessment of the risk/benefit balance of the product.
• In accordance with Article 15(2) and (3), expert reports must be provided on the analytical documentation, the pharmacotoxicological documentation, the residues documentation and the clinical documentation.
• All pre