Full-Service CRO Company
Quality Data Services, Inc. is a full service Contract Research Organization specializing in You – Your data, Your clinical trial, Your results.
With only the utmost QUALITY, we provide you with an experienced, professional team which launches your trial QUICKLY and dedicates itself to the trial’s successful completion. QDS has maximized efficiency in processes and procedures, and proudly boasts of key performance indicators.
|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
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 a Medical Device Research & Development Company looking for an outstanding CRO?
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 Information
Medical Device Research & Development Company
There is a lot to consider when looking for a CRO, whether you are a drug development company, biotech company or medical device research and development company. QDS can provide you with all of our CRO services or just the services you need for your project, such as pharmacovigilance services or monitoring services. This is not an industry where you can afford to cut corners when seeking quality clinical trial management. You need to make sure that the company you work with ticks every box. We certainly fall into this category for a lot of the drug trial companies. We have numerous years of relevant experience, as well as regional knowledge, experience with similar products and affordability. We also have an exceptional reputation in the industry when compared with competing contract research companies, which is something that we are very proud of. We would encourage you to contact us about some of the clinical data services that we have carried out thus far. While we cannot go into specific details because we are bound by confidentiality agreements, (which is something we take very seriously), give our clinical research organization a call and we will give you a deeper understanding of the way we operate and how we can assist your drug trial or medical device research company.
The clinical data services that we provide at our CRO company will go above and beyond to meet the expectations of your drug trial or device company
We provide an extensive collection of services, including full service CRO, integrated technology for clinical trials, and CRO pharmacovigilance services. This includes providing you with a clinical trial manager, who has many years of experience. We also offer a wide range of pharmacovigilance services, as well as being experts at providing data management in clinical research. Plus, if you need medical writing in clinical research you can rest assured that we have this expertise, too.
We are a clinical research organization that has many years of experience in CRO biotech
Are you a medical device research or drug development company seeking a clinical trial partner? At Quality Data Services, Inc., we have many years of experience in the CRO biotech industry, making us one of the most experienced CRO companies. We regularly partner with drug trial companies providing full service CRO.
We were established in 1995 as a contract research organization that provides:
- Medical writing services and reporting
- Biostatistical analysis
- Safety management
- Data management
- Clinical management
After more than 25 years in the industry, we have mastered providing high-quality CRO services. Most importantly, we adapt our service to suit you. It’s up to you whether you simply want us to complement your staff in certain areas or whether you are looking for a capable company to provide you with the complete package of clinical management services and clinical data services your project needs. We never try to operate via a one-size-fits-all approach. We will always adapt to your needs and requirements. This is why we are one of the leading clinical trial data management companies in the United States.
Looking for one of the best clinical trial management companies? We provide clinical project management services to many industry leading drug trial companies
If you need a company to provide you with full service CRO services including data management, project management services, and pharmacovigilance services we can assist. Unlike a lot of other clinical trial data management companies, we will be there every step of the way, from start to finish.
Our service always begins with a start-up, which consists of different elements, including:
- Source document creation
- Establishment of operations management
- Investigator assessment
- Site feasibility
- and much more
We will then help to manage your projects fully, finishing off with the study close-out.
This study close out involves:
- Regulatory document reconciliation
- Close out monitoring visits
- IRB close out reporting
- IP accountability & return/destruction
- Query resolution
Contact us today for more information about how we assist medical device research companies and our impeccable CRO pharmacovigilance services
If you would like more information about working with a CRO company with the services that we provide at our organization, please do not hesitate to get in touch with us. We have a friendly and experienced team who would be more than happy to answer your queries, no matter how big or small. You can reach us at 610-354-0404. Alternatively, you can send an email to firstname.lastname@example.org, and we will get back to you as quickly as possible. Your search for the best clinical trial management company is over.
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.