PARENT Methodological guidelines for development and governance of patient registries (09/08/2016; vs 1.0)

PARENT Methodological guidelines for development and governance of patient registries
General - Methodology
Patient registries, public health, research (epidemiology, clinical trials)
Guidelines for development and governance of patient registries
  • Cardiology/Vascular Diseases
  • Community care
  • Dental and Oral Health
  • Dermatology
  • Devices
  • Endocrinology
  • Emergency: medical
  • Emergency: trauma, surgery
  • Family Medicine
  • Gastroenterology
  • Genetic Disease
  • Hematology
  • Hepatology (Liver, Pancreatic, Gall Bladder)
  • Immunology
  • Infections and Infectious Diseases
  • Internal Medicine
  • Medical imaging
  • Mobility and frailty
  • Musculoskeletal
  • Nephrology
  • Neurology
  • Nutrition and Weight Loss
  • Obstetrics/Gynecology (Women’s Health)
  • Oncology
  • Ophthalmology
  • Orthopedics/Orthopedic Surgery
  • Otolaryngology (Ear, Nose, Throat)
  • Pathology
  • Pediatrics/Neonatology
  • Pharmacology/Toxicology
  • Physiotherapy and rehabilitation
  • Podiatry
  • Prevention and Wellness
  • Psychiatry/Psychology
  • Pulmonary/Respiratory Diseases  
  • Rheumatology
  • Sleep
  • Urology
  • Vaccines
  • Other (please specify)
General / any clinical domain
  • Clinicians
Public domain
  • English
not foreseen