Persly Research for post-marketing studies
No need to recruit againevery round
Patients' data refreshes with every hospital visit.
Pull the periodic report set for patients dosed with Keytruda between January and June 2026
Backed by
Reuse it for every periodic report
Data that refreshes with every hospital visit, so each round costs you less to collect.
Every field is already there
Pull together the fields a periodic report needs and put them to work. Build the report from them and file it.
Encounter- Department
- Diagnosis
- Visit date
- Lab result
Medication- Drug
- Dose
- Start date
- End date
Adverse event- Onset date
- Symptom
- Reason stopped
- Outcome
Fields captured (illustrative)
File it with the regulator
Once you have IRB approval, validate real-world outcomes, pull the cases together and file. We help you get there.
Frequently asked questions
- Is IRB review not required?
- The exploratory stage runs without review. Results are de-identified and counts for very small groups are not shown, so it does not constitute research using identifiable information. Once you settle on a hypothesis and move to the study itself, IRB approval is required.
- Is patient personal information visible?
- No. Every identifier is removed before analysis, counts for very small groups are not shown, and only the minimum clinically meaningful information is used.
- Can results be used for publications or regulatory submissions as is?
- Not as is. Once you have IRB approval, you can review the de-identified source records behind a finding and use them either as a citation in your paper or as supporting material in a regulatory filing. We help you prepare for that review.
- Where are patient records stored?
- Everything is stored encrypted, and records stay in the country the patient consented in.
