Professional Services
Elevate your clinical trials with our expert support
Our clinical trial software oomnia redefines how research is conducted, offering unparalleled support through features like professional assistance and infinite trial types support. Foster universal collaboration with an accessible interface designed for researchers, clinicians, sponsors, and participants alike. Stay at the forefront of your trials with real-time reporting and scale your endeavors limitlessly with oomnia’s infinite trial scalability. Trust in oomnia’s unwavering commitment to the highest data security, ensuring the confidentiality of your trial data. Experience a future where each meticulously crafted feature amplifies your research impact. Ready to revolutionize your clinical trials? Explore the possibilities with oomnia today.
Our protocol development service brings a multitude of benefits to your clinical trial process. This service streamlines and accelerates the protocol development phase. Moreover, it also ensures rigorous scientific accuracy, regulatory compliance, successful submissions, and seamless trial conduct for clinical data managers, study coordinators, biostatisticians, and most of all participants.
Wemedoo brings precision in crafting study objectives & endpoints. Our experts will help you choose the best outcomes & endpoints but the consult on the most effective design.
We are carefully delineating the methods, sequence, timing of data collection, and the participant journey. This aspect is frequently overlooked as essentials to trial success.
Wemedoo ensures that your trial protocol meets all ICH, EMA and FDA guidelines. We guarantee regulatory & ethical compliance & that your protocol submission goes smoothly.
Our expertly written statistical protocols ensure regulatory compliance, but also give the best chance of successfully meeting all the correct study endpoints.
oomnia - Meeting Industry Standards
Our unified clinical trial software is designed with compliance at its core, meeting critical industry standards. Our commitment to these regulations ensures that your clinical trials are not only efficient but also adhere to the highest levels of data integrity, privacy, and ethical conduct.
21 CFR
PART11
compliant
HIPAA
compliant
GDPR
compliant
ICH GCP
compliant
SWISS DATA PRIVACY LAW
compliant
FAIR ALCOA+
compliant
Considering Unified Clinical Trial Software?
Discover the unparalleled depth and sophistication of our professional services through a call with our expert team.
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