Regulatory Solutions

  1. Cosmetics Research And IRB Review 5/23/2022

    Institutional review board (IRB) review of cosmetics research is not always required, but it is considered best practice when human participants are involved.

  2. IRB Services For Federal Grants 3/22/2022

    Ensure expert oversight and experienced guidance when you select Advarra as your IRB of record when submitting your federal grant proposal.

  3. Streamline Your Regulatory Process 1/18/2022

    The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff, and institution documentation to streamline regulatory process and enhance compliance.

  4. Quality Center Of Excellence 12/17/2021

    As value chains extend around the globe, regulations evolve, and organizations feel the pressure to accelerate the speed at which they bring innovation to market; the need to maintain and optimize quality management systems has become more critical.

  5. Optimize Your Research Administration, Compliance, And Operations 12/2/2021

    Develop, implement, and uphold research compliance and administrative practices in alignment with federal regulations, state and local law, and industry best practices.

  6. TrialScope Disclosure Services 9/27/2021

    Whether you’re conducting 10 or 1,000 trials, that can mean juggling disclosure submissions for multiple registries. TrialScope Disclosure Services — protocol registration, results disclosure, plain language summaries, and redaction — make compliance manageable.

  7. Advarra Regulatory Consulting 6/10/2021

    Our regulatory consultants take action and move your research forward. If you’re looking for help in the development of innovative life science and digital health products, then Advarra® is the answer.

  8. Pharmacovigilance And Safety Surveillance 4/24/2021

    Delivering safety surveillance before and after regulatory approval for pre-approval and marketed health products.

  9. Get Help With Institutional Biosafety Committee Reviews 3/30/2021

    Crafting an IBC review involves the deliberate transfer of engineered genetic materials to human research subjects. Read Advarra's latest brochure on how they can assist with your next IBC review.

  10. IBC And Consulting Services 2/22/2021

    With a diverse roster of career biosafety professionals and a secure user-friendly submissions platform, Advarra routinely performs IBC reviews for gene therapy research in 10 business days or less from receiving a complete submission.