Products and Services

  1. Pharmacometric Services 6/27/2023

    Our talented and experienced team can assist in all Clinical Study Phases (Phase 0, I, II and III) and in study designs ranging from First in Human (FIH), Single Ascending Dose (SAD), Multiple Ascending Dose (MAD), Drug-Drug Interaction (DDI), Bioavailability/Bioequivalence (BA/BE), Food Effect as well as Special Population studies.

  2. TrialKit EDC 3/12/2024

    Modern clinical trials require modern technology. Leverage the flexibility and speed of the cloud with TrialKit electronic data capture (EDC).

  3. RegOps Services To Streamline Regulatory Submissions 5/28/2024

    Our RegOps team offers document-level publishing or management of the entire regulatory submission process. Coupled with our electronic document management system (Veeva), we can oversee all technical aspects for submission of your dossier (eg, eCTD document granularity, utilization of content templates, document formatting, hyperlinking, bookmarks, navigation, publishing, and redaction services).

  4. MRN Technologies 11/22/2024

    Our research is powered by MRN owned, regulatory-approved and validated eClinical software systems. Our technology can be used at-site and at-home enabling fully integrated data through any clinical trial.

  5. Targeted Source Data Verification 2/6/2025

    Ergomed’s Risk-Based Clinical Monitoring and Source Data Verification Approach for Data Integrity

    Ergomed ensures the highest data integrity and patient safety standards through our risk-based clinical monitoring and Source Data Verification (SDV) practices. SDV is a critical process in clinical trials that ensures the data collected are accurate, complete, and verifiable against the source documents. We compare data entered into case report forms or electronic data capture systems with the source data to confirm their accuracy and reliability.

  6. Pharmaceutical Contract Packaging Services: Capacity

    Hard work is just part of the Ropack Pharma Solutions ethos, and we prove it daily through our output: high-capacity turnover that does not compromise our quality or excellence. We provide ample capacity and bring agility, efficiency and gold-standard technology to the manufacturing and packaging of solid oral dosage forms for clinical and commercial pharmaceutical applications and commercial nutraceuticals.

  7. Medical Writing Software 6/17/2025

    Accelerate Medical Writing Without Compromising Accuracy or Compliance

    In the fast-paced world of clinical research, the ability to produce, review, and finalize high-quality documents—on time and with full regulatory compliance—is non-negotiable. Ideagen Document Review (formerly known as PleaseReview) is the trusted collaboration and co-authoring platform that enables clinical teams to streamline document reviews, reduce version chaos, and ensure traceable, auditable feedback across the board.

  8. Get The Right Participants For Your Study Easier And Faster 1/22/2025

    Clinical trial recruitment solution: Get the right participants for your clinical research study easier and faster than ever before.

  9. Get Phase-Appropriate CMC Support 9/20/2023

    Strategic product development and CMC regulatory planning start early on at the pre-IND stage and apply to the entire development lifecycle through to post-approval.

  10. Medical Writing For Clinical Trials 1/25/2024

    For successful regulatory outcomes, we provide quality medical writing services for clinical trial documents, safety updates, and marketing applications.