Full-Service CRO Company
Founded in 1995, Quality Data Services, Inc., a contract research organization company (CRO companies), offers clinical management, clinical monitoring, safety management, data management, biostatistical analysis, biostatistical reporting, and medical writing services for clinical research studies. We offer the top clinical data services amongst all clinical research organizations, specializing in CRO biotech.
| Department | Task | Timeline |
| Clinical Project Management | Final Protocol to First Patient In | 3 weeks |
| Clinical Data Management | Final Protocol to Validated Database (Go-Live) | 3 weeks |
| Monitoring/Data Management | Last Patient Out to Final SDV/Database Close | 1 week |
| SAS Reporting | Database Close to TLF Generation | 3 days |
| Statistical Analysis | Database Lock to Statistical Analysis | 2 weeks |
| Medical Writing | Stat Analysis Results to Draft CSR | 2 weeks |
WE’LL ENSURE YOU ALWAYS GET
BEST RESULTS.
We are the experts in communication for clinical trials.
Our professional staff is here to assist you in accuracy and speed.
Our team has the combined years of experience and knowledge to assist you
Our company is a certified woman-owned business.
Are You Looking For A Trusted CRO To Help With Your Company’s Needs?
CRO Biotech services from Quality Data Services, Inc.
If you are looking for quality clinical trial data services and one of the best CRO companies, you have come to the right place. At Quality Data Services, Inc., we will be your full-service partner throughout the clinical trials that you carry out and demonstrate that we are the best clinical trial management company you could hire. There’s a lot to know about working with clinical trial data management companies and medical device research and development companies. We provide many different services, including full service CRO support at our clinical research organization, which includes a fully certified Integrated Technology Platform. So you can see why we are one of the best CROs in support of Biotech and Drug Trial companies in the United States.
Additional InformationQuality Data Service Offers Complete Remote Clinical Data Services
As one of the top clinical research organizations, we can offer you complete clinical management services or we can offer our services to work alongside your clinical and administrative staff. Our CRO biotech offers three options, regarding procedures and templates:
- Bring your procedures and templates
- Customize our procedures and templates to your needs
- Utilize our processes and templates as-is.
Our full-service clinical research organization specializes in you – your data, your clinical trial, your results.
Quality Clinical Data Services Focused on Quality and Efficiency
At Quality Data Services, we focus on providing each organization with the highest-quality CRO experience, possible. Our qualified team of 50 professionals has more than 100 years of experience, combined and more than eight professional certifications. We can assure you we can provide you with seamless and efficient project planning and implementation. There is no other CRO company that can offer you our level of experience and education.
Marshaling our innate accuracy and speed, we quickly launch your clinical research trial, then dedicate ourselves to its successful completion. Quality Data Service builds maximized efficiency into its processes and procedures. We regularly meet and exceed your key performance indicators (KPIs) with our clinical data services. Our dedication to each project sets us apart from other clinical research organizations.
How We Deliver Timely, Effective Results
Of course, the length of time needed for you to test your medication or medical device differs, but we set rigorous deadlines for ourselves to provide you with the clinical trial components to support your medication or medical device study. We offer some of the most efficient processes among clinical research organizations.
Our Projected CRO Biotech Timeline
In 3 weeks: Final Protocol to First Patient (Clinical Project Management)
In 3 weeks: Final Protocol to Validated Go-Live Database (Clinical Data Management)
In 1 week: Last Patient Out to Final SDV/Database Close (Clinical Monitoring/Clinical Safety Data Management)
In 3 days: Database Close to TLF Generation (SAS Reporting)
2 weeks: Database Lock to Statistical Analysis (Statistical Analysis)
2 weeks: Stat Analysis Results to Draft CSR (Medical Writing)
Quality Data Services Offers Significant Experience
At Quality Data Services, we’ve managed more than 1,000 clinical trials, providing full-service CRO. Our company offers expert communication for clinical trials that other CRO companies can’t.
We don’t simply offer remote support. We offer a full-service CRO biotech partnership throughout your clinical trial, whether you operate a medical device or drug trial in the United States.
Clinical trials for Food and Drug Administration (FDA) approval require a lengthy, expensive process. We know that you can’t afford unnecessary delays or additional red tape, so we developed some of the top methodologies among clinical research organizations in the US. We developed efficient, cost-effective products and procedures to help companies like yours administer your clinical trials efficiently and effectively.
We’ve proven our methods and process with more than 1,000 successful clinical trials. You can trust our experience, methods, and dedication to helping you and your clinical trial succeed. Our flexible methods for full-service CRO guarantee you can use the protocols you need with our data collection, analysis, and clinical research writing.
Contact Us
Contact us today to learn how Quality Data Services can help you administer your clinical trial for medical devices or medications. Call us at 610.354.0404 or email us at info@qdservices.com for the best clinical services available. Let us help you bring your medical device or medication to market. We’ll show you what makes us one of the top clinical research organizations in the country.
If you want a CRO that is experienced, with a proven track record that you can trust, come to us. We help biotech companies reach their full potential by offering highly skilled and professional project managers to help them push through their drug and medical device research trials. We are one of the top CRO companies providing pharmacovigilance services because our managers and staff have over 100 years of experience to offer. We will keep your drug trials or medical device research and development progress on track. Our experience is exceptional.
Get the Most Out of Our CRO Services for Your Medical Device Research and Development
We are a full-service CRO. Our services include:
- Project management
- Clinical site management and monitoring
- Safety management
- Clinical data management
- Biostatistics, Analysis & reporting
- Medical writing
- Full CDISC, SDTM and ADaM reporting services
- Remote clinical solutions
To see just how much of an impact we can have on your clinical research goals, check out our service page.
When you choose us, you are receiving a dedicated partner. Your success is our success. We leverage experience, standard and efficient procedures for rapid start-up and execution. No fluff and no-nonsense approach to research. Another advantage of working with us is that we will ensure everyone stays on schedule. With so many moving parts taking place during a trial, it is easy for everyone to feel like they’re on their own. Our experienced staff can ensure that everyone knows what their tasks are and when they need to be completed. We make sure that everyone is working together to be as productive as possible. In addition, we will assign you the same team from start to finish. This further ensures that there are no missed details from phase to phase.
Get Your Trials on Track Today
To experience what a stream-lined drug and clinical trial is like, contact our team today. We will keep your trials on-schedule and on-budget without sacrificing quality.
Quality Data Services (QDS) offers the best medical device market research services for biotech and drug trial companies in the United States.
QDS is among the top clinical research organizations (CRO) providing full service CRO research and development. Whether your company project requires full service CRO biotech facilities or drug trial services, QDS can support your endeavor.
Consider our collection of medical device market research services:
- Full Service CRO: We conduct data management and project management services from start to finish.
- Integrated Technology: Our IT services enhance your existing medical database.
- Seasoned Professionals: We have clinical trial managers with experience from the top clinical research organizations to assist with your clinical data research.
- CRO Pharmacovigilance: We offer safety management systems to monitor all drug effects and compare them against existing entries in a comprehensive CRO pharmacovigilance database.
Medical Device Market Research
Our CRO biotech and drug trial services provide insight into the comprehensive process of clinical data research. Our seasoned professionals help companies avoid delays and red tape for productive research practices.
Top Full Service CRO Company
QDS services are ideal for biotech companies that want to improve their medical device research practices.
Medical Device Research and Development Services
Successful medical device research and development projects require constant maintenance. They are lengthy processes requiring services from only the top CRO biotech companies to effectively perform.
QDS services include continuous development to ensure the best management, oversight, facilitation, and communication at every stage of medical device market research.