Avania ensures your data is well-structured, clean, consistent, and in the correct format to support the claims in your clinical study report. Committed to delivering within set timelines, we routinely accomplish clean database lock within days of Last Patient Last Visit.

View our presentation on the persuasive power of data visualization across the clinical trial management spectrum:

View the Presentation Slides

Watch the Webinar

Your product is important, and it takes a team with data analytics expertise to move it forward. It Takes Avania.

Schedule a Meeting With Our Experts

Conducting a clinical trial is overwhelming; meeting critical milestones, managing your budget, and speeding your product to market. With Avania, you’re partnered with a project manager who drives the entire trial execution team. With their effective leadership skills and industry expertise, our project managers excel in the oversight of trial conduct, progress reporting, risk mitigation, and budgeting. Our project managers are adept at providing excellent client service and proactive communication.

Your product is important, and it takes a team with clinical trial expertise to move it forward. It Takes Avania.

Schedule a Meeting With Our Experts

Innovation of medical products requires a planned, staged approach from concept to commercialization. You want your new investigational device to become the standard of care and enhance patients’ lives. Consult with Avania for a strategic, coordinated approach to ensure your clinical development process and market introduction go smoothly.

Our experienced team of therapeutically aligned medical writers support your product development by optimizing your presentation of clinical information with a wide variety of medical and scientific documentation. Our flexible services are available as part of your comprehensive program or as stand-alone assignments.

Avania’s expert medical writing team compiles, organizes, writes, edits, and produces documentation for study design, postmarket surveillance and clinical follow-up, clinical evaluation, study results, scientific literature, and investigator’s brochure.

Your product is important, and it takes a team with specialized medical writing expertise to move it forward. It Takes Avania.

Schedule a Meeting With Our Experts

All businesses are unique — consistency and reliability are critical to ensuring quality. Whether you are part of an emerging company or a long-established multinational corporation, Avania can ensure your quality system fits your organizational structure.

Your product is important, and it takes a team with quality management expertise to move it forward. It Takes Avania.

Schedule a Meeting With Our Experts

Avania’s experienced team of regional experts will partner with you to support your business objectives. Our regulatory specialists will deliver an efficient and effective regulatory strategy — and assist with submissions — enabling you to negotiate the process smoothly and efficiently.

Avania will help you research the current reimbursement climate for your product and plan early, so you can begin generating revenue as soon as possible after clearance. Our world-class research and reimbursement programs advance your medical devices, novel technologies, and combination products in Europe, the U.S., and Australia. Not only do we work with you to develop a winning strategy, but we will help you access reimbursement channels for your products.

Your product is important, and it takes a team with expertise in reimbursement strategies to move it forward. It Takes Avania.

Schedule a Meeting With Our Experts