Company Collateral & News Releases
IMARC Research is committed to being an industry thought leader and publishes collateral on a wide-range of clinical research topics. We welcome and encourage you to visit and download these documents for reference.
IMARC Expands Service Offerings
IMARC Research, a contract research organization based in Strongsville, Ohio, announced that it has launched independent oversight capabilities by adding Data Safety Monitoring Boards (DSMBs) and Clinical Events Committees (CECs) to its existing monitoring, auditing, training, project management and consulting services.>
IMARC Signs Agreement with European CRO
CROs expand combined resources, services and expertise
IMARC Research and TheraGenesis GmbH of Sutensee, Germany have signed a collaboration agreement to integrate and expand their combined resources, services and expertise in the development of medical devices. The agreement is solely a work-based collaboration with neither firm holding a financial stake in the other.
IMARC Research Names Assistant Director
CLEVELAND, Ohio — IMARC Research, a Strongsville-based contract research organization has named Stephani Hulec its Assistant Director of Clinical Monitoring Services.
IMARC Research Achieves ISO 9001:2008
IMARC Research has announced that it has attained ISO 9001:2008 status.
Following the same process as manufacturing companies, IMARC spent more than a year and involved its entire staff of nearly 30 persons in pursuing the designation. “We invested significant dollars and hundreds of hours of staff time in the process,” said Sandra Maddock, IMARC CEO and president.
Cardiovascular Expertise Sell Sheet
Conducting cardiovascular clinical trials?
Clinical trials conducted in the Cardiovascular (CV) arena are challenging, first and foremost, due to the variety of underlying disease states and conditions that affect a majority of potential trial participants. IMARC was built upon a regulation-focused compliance foundation and has an expansive resume, which touts several therapeutic verticals, including CV.
IMARC Research Expands Staff
CLEVELAND, Ohio — IMARC Research, a clinical monitoring firm based in Cleveland, has announced the addition of seven new clinical research associates (CRAs) and one member of its business staff. In addition to all seven belonging to the Society of Clinical Research Professionals (SoCRA), three of the seven new IMARC CRAs also hold advanced degrees.
General Brochure
Approval. That's what you're after
We are, too: Your FDA or Worldwide approval. You will also approve of our ability - and effectiveness - in preparing, educating, complementing and guiding your trial team.
Auditing Sell Sheet
Finally, Being Audited Pays Off
With FDA and International inspections on the rise, so are stress levels of everyone involved in clinical studies. IMARC provides the specialized independent auditing support services you need to survive today's rigid regulatory requirements — not only to ensure compliance, but also to protect patients.
Consulting Sell Sheet
Balanced Thinking + Inventive Ideas = Boosted Productivity for Clinical Studies
These are just some of the value-added components IMARC injects into our consulting services. Tap into our knowledge base and ensure that what works gets done and what doesn't work gets bounced.
Monitoring Sell Sheet
Hit Your Marks with IMARC
Reaching benchmarks isn't enough. It is how you reach them that matters. With IMARC Monitors protecting your interests from Day One, your data integrity is ensured, compliance requirements enforced and patient safety entrusted.
Research Training Sell Sheet
You Need to Reach the Finish Line.
Like Anything Else, that takes training
Your study may be short staffed, operating on a tight budget. but it can't afford to be derailed due to lack of experience or knowledge. IMARC offers training and development programs to get your clinical research staff up to speed fast.
FAIR Shake™ Sell Sheet
A 4-Point Training Program
to Navigate Through Regulations
The FAIR Shake™ technique takes an otherwise complicated maze of requirements and breaks them down into four simple areas that can be applied to clinical research questions.
Executive Summary
IMARC assists the clinical research community in the pursuit of FDA and worldwide approvals
We control the complex management of trials via cost-effective monitoring, auditing and training services — which results in the support, proof and assurance they seek to overcome chaos caused by complexity while achieving compliance through consistency.
