Observational, Data Collection Study for Subjects With Diabetes Using Insulin Injections

Inclusion Criteria: 1. Documented T1D or T2D for at least 1 year prior to study enrolment 2. T1D: Subjects aged 1 year or older 3. T2D: Subjects aged 30 years or older 4. A1c at inclusion ≤ 10% 5. Subjects using basal-bolus MDI therapy or basal insulin only - basal insulin Lantus or Tregludec and any short acting insulin. * T2D: Insulin pumps will also be accepted. 6. T2D: BMI ≥ 25 kg/m2 7. Subjects willing to follow study instructions: 1. For SMBG users: measure capillary blood glucose at least 4 times a day and twice a week 7-point profile. Document blood glucose level, insulin delivery, meals and daily activities. Optional: wear blinded CGM. 2. For CGM users: Document insulin delivery, meals and daily activities. Optional: Measure capillary blood glucose in addition. 8. Adult subjects or parents of pediatric subjects willing and able to sign a written informed consent form. Exclusion Criteria: 1. An episode of diabetic keto-acidosis within the month prior to study entry and/or severe hypoglycemia resulting in seizure or loss of consciousness in the month prior to enrolment. 2. Concomitant diseases/ treatment that influence metabolic control (except diabetes treatment for T2) or any significant diseases /conditions including psychiatric disorders and substance abuse that in the opinion of the investigator is likely to affect the subject's ability to complete the study or compromise subject's safety 3. T2D: eGFR \< 60 4. Participation in any other interventional study 5. Female subject who is pregnant or planning to become pregnant within the planned study duration 6. T1D: Subject is in the "honeymoon" phase - i.e. less than 0.5 insulin units/kg per day. 7. Drug or alcohol abuse.