Partnering Solutions

  1. Regulatory Submissions
    Regulatory submissions are the most critical milestones in your clinical research program. Quality submissions can accelerate time to market, bring the benefit of new treatments to patients sooner, maximize research investments, and conserve patent life.
  2. Clinical Trial Packaging Brochure

    For more than 20 years, Bellwyck has been a true partner in developing smarter solutions for the pharmaceutical industry — from clinical trial to commercialization. We utilize cost-efficient packaging strategies to launch clinical studies on time, every time. Discover all of the ways in which Bellwyck might assist you in meeting your unique objectives.

  3. eClinicalGPS

    eClinicalGPS is designed to automate and streamline clinical site payments, getting sites paid faster and more accurately with less administrative burden. Configured

  4. Real World Data For Safety Surveillance

    UBC has focused on drug safety evaluation with RWD for more than 15 years and is aligned with FDA’s Sentinel Initiative. UBC’s safety scientists and epidemiologists provide comprehensive and customized RWD solutions to evaluate the safety of your marketed products.

  5. How Biorasi Optimizes Clinical Solutions

    Best-in-class processes coupled with industry-leading technology to fight for your trial’s success.

  6. Clinical Trial Packaging & Labeling

    With unrivaled experience in packaging and labeling, PCI combines knowledge, experience, and innovative technologies ensuring our ability to supply high quality products reliably and effectively wherever in the world our clients need them.

  7. Rho Vaccine Studies

    Rho is 1 of 5 contract research organizations in the BARDA Medical Counter Measures (MCM) Clinical Studies Network (CSN) ID/IQ multiple award task order contract (MATOC) pool that designs and conducts clinical studies needed to develop medical countermeasures—drugs, vaccines, and diagnostic tests—that help protect public health against bioterrorism, pandemic influenza, and other emerging infectious diseases.

  8. Post Approval Studies
    Whether you’re working to provide new treatment options through label extensions or trying to demonstrate efficacy over other marketed medications, Rho has the research power that will advance your Phase IV clinical trials.
  9. Clinical Trial Material Distribution Services

    As your clinical material partner, we simplify – and accelerate – your clinical trials. From assistance with time-consuming international documentation through destruction following all regulatory protocols, RPS is your trusted clinical trial partner.

  10. Site Contract Management From Syneos Health

    At Syneos Health, we know that negotiation of a site contract is a relatively simple process, which often has an incredibly high number of unintentional complications. Read why many sponsors have entrusted Syneos Health to build a dedicated team with customized tools and processes to provide functional site contracts management services in alignment with their unique R&D strategies and needs. We can help to streamline negotiations and ensure that contract and budget executions are no longer the rate limiting factor in how quickly patient enrollment can begin.