MedNet is proud to partner with leading Clinical Research Organizations (CROs) and healthcare consultants from around the world through the iMedNet Partner Program. We carefully select each Partner based on their proven track record of successfully meeting sponsors’ clinical study needs, as well as their demonstrated expertise in configuring studies within the iMedNet EDC environment. All Partners have certified iMedNet Designers on staff who are fully trained on the capabilities of the iMedNet EDC solution.
Life science companies that are looking for trusted experts to help them with iMedNet EDC system design, testing and deployment need look no further than our iMedNet Partners. These organizations can provide a wide range of value-added services, from standalone iMedNet EDC design and validation services to more comprehensive solutions that couple their superior clinical research services with MedNet’s highly efficient and user-friendly iMedNet EDC platform.
Current Partners Include:
|Headquartered in Rockville, Maryland, Accelovance is a privately held company that has developed a unique operational approach for delivering quality, on time, and cost effective clinical studies. The company was recognized as “Best CRO” with consecutive Industry Excellence awards in 2009, 2010 and 2011. Accelovance tailors its full offering of CRO services to present a clinical solution that meets a sponsor’s needs. Accelovance has a 100% owned subsidiary providing CRO services in China. These capabilities can assist clients with global development programs or product registration in China, the fastest growing pharmaceutical market in the world. For more information, visit the company’s website at www.accelovance.com.|
|Founded in 1996, Advance Research Associates has been a trusted clinical research partner (CRO) to the pharmaceutical, biotech, and medical device industries for over fifteen years. In the years since its inception, ARA has provided a spectrum of innovative solutions and has lent its expertise in data management and biostatistics across a wide range of projects for all study phases. ARA works as an extension of the client team, ensuring that clinical study timelines, costs, and project requirements are met. As a CRO for over 150 companies and having supported over 350 studies, ARA prides itself on delivering a high-quality product that has led to 70% of our business coming from repeat clients. For more information visit www.advanceresearch.com.|
|Advanced Clinical provides full-service CRO and strategic resourcing solutions for the life sciences industry. With 15+ years of experience, Advanced Clinical is an established presence in the clinical research field, providing services specifically for pharmaceutical, biopharmaceutical, biotechnology and medical device organizations. Advanced utilizes a value-based, “One Team” approach. To learn more, visit www.advancedclinical.com.|
|KCD2 Group, providing independent consulting services in clinical database development and reporting, has 12 years of experience with medical device trials, from study initiation to database lock. KCD2 will work closely with your clinical team to address your needs with CRF/eCRF design, database design/development, and reporting, ensuring they have the data and information they need to succeed. Services provided include: CRF/eCRF design, data management plans, database design and development, and report design and development. KCD2 can help lower your costs, provide fast turn-around, and deliver the flexibility you are looking for. For more information, visit www.kcd2group.com.|
|NAMSA has provided services to medical device manufacturers for 45 years, specializing in material safety testing and consulting. Through acquisition, NAMSA added comprehensive regulatory and quality systems support, expanded functional studies with state of the art imaging capabilities, full clinical research services with contract field clinical engineers, and expanded educational services including physician and sales training. NAMSA continues to enhance medical product development by guiding inventors and manufacturers on the most efficient path to commercialization. To learn more, visit www.namsa.com.|
|Oncotherapeutics is a full service Contract Research Organization (CRO) that specializes in therapeutic oncology. Their senior level clinical research teams are overseen by nationally recognized research oncologists and key opinion leaders in the field. Additionally, Oncotherapeutics has regionally based senior level clinical trial monitors with expertise in all therapeutic oncology areas. The company offers comprehensive services for preclinical and phase I-IV clinical trials, and can customize its approach to meet individual client needs. For more information, please visit
|Prairie Education & Research Cooperative (PERC) was founded in 1983 to facilitate cardiovascular and vascular clinical research. PERC was conceptualized to integrate state of the art medical research and bedside patient care. From its conception, PERC has provided intelligent direction, skillful execution, proven results and diverse research activities. To facilitate these research endeavors, PERC has been instrumental in fostering new cooperative efforts between physicians, medical industry, and the clinical research community. In this regard, PERC’s personnel have promoted the clinical introduction of new pharmaceuticals, cardiovascular techniques and medical devices. PERC is an excellent resource for project, site and data management. PERC is dedicated to conducting each and every trial with intelligent direction, skillful execution, and proven results: The hallmarks of the PERC organization. For more information, visit www.thepercdifference.com.|
|Statistics & Data Corporation (SDC) provides innovative biostatistics and clinical data management services to pharmaceutical, biotechnology, and medical device companies, as well as CRO partners. SDC is committed to providing experienced teams who take ownership of deliverables and provide positive engagement on projects. SDC delivered on-time on over 99% of key project milestones since 2010, and has a proven track record for rapidly delivering analyses during project closeout (consistently providing top-line analysis within 3 business days of database lock). To learn more, visit www.sdcclinical.com.|
|SPIRITT is a specialty clinical research team focused on collecting high-quality patient-informed evidence in the medical device, biologic and pharmaceutical industries. SPIRITT Research offers full or a la carte services for medical practices (community-based and academic) and industry sponsors, including: clinical study development and execution services; subject engagement and compliance; regulatory guidance; product development; educational training/support services; abstract preparation/podium presentation assistance and peer-reviewed journal publication assistance. It is SPIRITT’s goal to help researchers and clinicians collect evidence that will improve healthcare outcomes for patients while meeting the needs of other stakeholders, including healthcare providers, payers and medical technology companies. For more information, please visit www.spirittresearch.com.|