Home

Full-Service CRO Company

THE PARTNERSHIP
BEGINS WITH YOU.

KEY PERFORMANCE WITH SPEED 100%

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.

LEARN ABOUT OUR
TIMING & TASKS

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.

1000 +

Clinical Trials

We are the experts in communication for clinical trials.

50 +

Professional Staff Members

Our professional staff is here to assist you in accuracy and speed.

100 +

Years of Experience

Our team has the combined years of experience and knowledge to assist you

8 +

Certifications

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

Looking for the best CRO companies for full service CRO

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, as well as biostatistical analysis, safety management, data management, monitoring, and 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 study start-up, which consists of many 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. The latter includes regulatory document reconciliation, close out monitoring visits, IRB close out reporting, IP accountability & return/destruction, as well as 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 info@qdservices.com, and we will get back to you as quickly as possible. Your search for the best clinical trial management company is over.