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Full name of the regulatory document.

Showing 20 pages using this property.
A
AVG – Allgemeines Verwaltungsverfahrens-gesetz  +
U
Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff  +
N
Article from Mora et al.  +
A
D
BGB - BĂŒrgerliches Gesetzbuch  +
F
Bonnes pratiques - CONTRÔLE QUALITÉ À DISTANCE DES ESSAIS CLINIQUES (CNIL)  +
D
Bundestag - Sachstand zur Aufbewahrung von Patientenakten in der ambulanten Praxis Fristen und Form  +
E
CHMP Guidelines  +
C
CIOMS - International Ethical Guidelines for Health-related Research Involving Humans  +
CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects  +
CIOMS Publications  +
E
COMMISSION IMPLEMENTING DECISION (EU) 2022/729  +
U
CTCAE - Common Terminology Criteria for Adverse Events  +
G
Clinical Trial toolkit  +
Clinical investigations of medical devices – compiling a submission to MHRA  +
F
Code de la SantĂ© Publique - Partie RĂ©glementaire - 1ere partie, Livre 1er, Titre II  +
Code de la SantĂ© Publique - Partie lĂ©gislative - 1ere partie, Livre 1er, Titre II  +
Constitution du 4 octobre 1958  +
D
DGEPi - GEP Guter Epidemiologischer Praxis  +
F
DHOS/E1/DAF/DPACI no 2007-322  +