The leading Authority in
Clinical / Medical Data
Dr Bart Ripperger is the leading authority in bridging the gap/ divide between healthcare providers who are generating clinical data and teams at pharma and medical device companies who are evaluating and analyzing clinical data. Many clinical data details and challenges are not fully appreciated by teams evaluating clinical data (details in videos on upcoming pages.)
Dr Bart Ripperger assists researchers, pharmaceutical and medical device companies to Real-time Stream this highest quality, structured clinical data using the Starwriter Patented Process, of which Dr Bart is the Co-creator.
Starwriter assists pharma + medical device companies with :
- Speed/ Real- time streaming of data
- DCTs- fully remote ( Decentralized Clinical Trials)
-HEOR /Health Economics and Outcome
-RWE (Real World Evidence)/ RWD ( Real World Data)
-VEO (Value Evidence Outcomes
-Post Market Surveillance
-Safety/Pharmacovigilance (including real time adverse event reporting-MD3500,E2B)
-PRO ( Patient Related Outcomes)
-Pharmacoeconomics
-Automated Investigational Drug study assistance
-Medical Writing:
Regulatory - Automated - most docs for clinical trials, FDA, EMA approval: NDA, BLA, ISS, ISE all CTD and others
Medical Affairs/Educational - Manuscripts, White papers, brochures and more
-Drug Repurposing
Are you facing the challenge of real-time streaming highest quality, standardized and structured clinical data for evaluation and analyses of your company's products ?
Dr Bart and Starwriter assist using our Patented Process !
Clinical / Medical Data
Dr Bart Ripperger is the leading authority in bridging the gap/ divide between healthcare providers who are generating clinical data and teams at pharma and medical device companies who are evaluating and analyzing clinical data. Many clinical data details and challenges are not fully appreciated by teams evaluating clinical data (details in videos on upcoming pages.)
Dr Bart Ripperger assists researchers, pharmaceutical and medical device companies to Real-time Stream this highest quality, structured clinical data using the Starwriter Patented Process, of which Dr Bart is the Co-creator.
Starwriter assists pharma + medical device companies with :
- Speed/ Real- time streaming of data
- DCTs- fully remote ( Decentralized Clinical Trials)
-HEOR /Health Economics and Outcome
-RWE (Real World Evidence)/ RWD ( Real World Data)
-VEO (Value Evidence Outcomes
-Post Market Surveillance
-Safety/Pharmacovigilance (including real time adverse event reporting-MD3500,E2B)
-PRO ( Patient Related Outcomes)
-Pharmacoeconomics
-Automated Investigational Drug study assistance
-Medical Writing:
Regulatory - Automated - most docs for clinical trials, FDA, EMA approval: NDA, BLA, ISS, ISE all CTD and others
Medical Affairs/Educational - Manuscripts, White papers, brochures and more
-Drug Repurposing
Are you facing the challenge of real-time streaming highest quality, standardized and structured clinical data for evaluation and analyses of your company's products ?
Dr Bart and Starwriter assist using our Patented Process !
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Expertise in:
Automating and real-time streaming of highest quality,standardized and structured clinical data for analysis to prove safety, efficacy and value of your company's products. Using medical data to prove value based care and advance evidence based medicine. Please complete form today to learn how we can assist with your company's medical data needs |
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