Regulatory Solutions

  1. NDA/MAA Preparation Survival Guide: Three Guiding Principles 9/8/2022

    No two marketing application (NDA, BLA, MAA, NDS, jNDA, etc.) projects are ever the same. From our years of experience preparing more than 120 marketing applications, Veristat has learned there are three constants you can count on.

  2. Balancing Compliance Among The Shifting Sands Of Pharmaceutical Data Privacy Regulations 8/26/2022

    Maximize compliance, increase revenue potential, and improve patient safety by leveraging proven technology.

  3. Bring More Confidence To Your Post-Marketing Pharmacovigilance And Safety Surveillance 8/1/2022

    Discover our records of success in PV excellence and experience so you can have certainty that our team will address your PV needs comprehensively and proficiently.

  4. The Importance Of A Trusted Pharmacovigilance Partner 8/1/2022

    Veristat supports successful post-marketing pharmacovigilance (PV) expertise for pharmaceutical drugs, biologics, natural health products, and medical devices.

  5. Global Advantage With Free Trade Zones In China 7/14/2022

    Understand how free trade zones work, and explore a flexible and cost efficient way to supply clinical trials in China and around the globe.

  6. Mitigate Risk With Research Billing Compliance Services 6/23/2022

    Ensure you are billing for clinical research confidently and in compliance with federal requirements by utilizing Advarra’s Institutional Research Center of Excellence (CoE) Consulting Services.

  7. 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.

  8. Revvity Signals Software Solutions For Pharmacovigilance And Drug Safety 5/13/2022

    Strategically transform your medical review, safety review, and compliance monitoring processes with our innovative solution for Pharmacovigilance.

  9. 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.

  10. 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.