+1 919.998.3860

RFP@cenduit.com

www.cenduit.com

Global Sales and Marketing

THE CENDUIT PATH TO PATIENT DRUG COMPLIANCE IN YOUR CLINICAL TRIALSSMARTER SOLUTIONS, SMOOTHER STUDIES

& COMPLETE CONTROL.

Conducting a clinical trial is complicated enough without having to deal with problems and setbacks. With Cenduit you can focus on your trials, not tribulations.

Whether you are developing a vaccine or a biotech product, or running an early-phase or late-phase study, we will design a smart process and a smart system tailored to the needs of your trial. Our unique combination of clinical operations and clinical supplies expertise and our study-specific approach to project management will help you ensure seamless patient enrollment, randomization and drug supply management.

CLINICAL INTELLIGENCECenduit’s reporting module

• Intelligent reports that provide useful information for decision making

• Integration with EDC, labs and logistics data for complete picture

• Reports that are fully configurable by the user - build your own dashboard to track your trial progress• Automated alerts to your desktop• All in real time

QUALITYCenduit’s focus

• 21CFR Part 11-compliant• Fully validated system build process• Built-in Quality Assurance• Routine, automated data checks

throughout trial process• A Quality First culture

Ha

pp

ier Site

sCLINICAL SUPPLIESCenduit optimizes the use of all available materials

• Control of release through integration with GMP inventory

• Control of multiple storage facility inventories in global trials

• Control of expiry dates• Pooling of study medication• Management of ancillary materials and lab kits• Visibility of cold chain supplies

- Tracking to kit level

ACCESS TO EXPERTISECenduit project management

• U.S. and European project management offices established 10 years

• Consultation on trial design and system solutions

• 24/7 Helpdesk• Multilanguage capability

HAPPIER SITES.

We know that what matters most is our ability to make sites feel confident and in control, which leads to improved protocol compliance, less wastage and better site performance. Don’t rely on trial and error. Conduct smoother, happier trials with Cenduit.

EASE OF USE FOR INVESTIGATOR SITESCenduit’s interactive response technology

• Web access with phone backup• Drug logistics management• Patient screening, randomization

and visit management• Patient drug assignment

• Treatment unblinding• Drug accountability and

returns management• Integration with EDC• Study simulation and forecasting

Sma

rter So

lutio

ns

THERAPEUTIC EXPERTISE • Anti-Inflammatory• Asthma• Bone Diseases• Cardiovascular• Central Nervous System• Diabetes• Endocrinology• Immunology & Infectious Diseases• Metabolic Diseases• Nephrology• Oncology• Pain • Pediatrics• Psychiatric Disorders• Respiratory & Pulmonary • Rheumatology

STUDY-SPECIFIC EXPERTISE• Phase I-IV• Complex Dosing• Vaccines• Biosimilars• Investigator-Led• Complex Randomization Designs• Open Label

EVERY PATIENT. ON TIME. EVERY TIME.

There is no room for error when randomizing patients and assigning them treatment. For this reason, quality assurance is at the foundation of everything we do. We will always randomize patients into the right treatment group, we will always assign them the correct medication, and we will always ensure that the medication is available for them every time they need it.

Our quality procedures include oversight of the entire IRT system setup and validation process as well as ongoing statistical monitoring of all studies to ensure absolute clinical protocol compliance.

We help our sponsors take control of their trials while eliminating the tribulations. That is Cenduit’s commitment to quality and to the success of your trial.

Every Pa

tien

t. On

Time. Eve

ry Time.

Randomization of the patient into the correct treatment group

Assignment of the correct medication to the patient

Availability of the medication at the clinical site when the patient needs it

CENDUIT’S QUALITY COMMITMENTCenduit helps its sponsors control the most important elements in a clinical trial:

SMARTER SOLUTIONS, SMOOTHER STUDIES & COMPLETE CONTROL.

Conducting a clinical trial is complicated enough without having to deal with problems and setbacks. With Cenduit you can focus on your trials, not tribulations.

Whether you are developing a vaccine or a biotech product, or running an early-phase or late-phase study, we will design a smart process and a smart system tailored to the needs of your trial. Our unique combination of clinical operations and clinical supplies expertise and our study-specific approach to project management will help you ensure seamless patient enrollment, randomization and drug supply management.

CLINICAL INTELLIGENCECenduit’s reporting module

• Intelligent reports that provide useful information for decision making

• Integration with EDC, labs and logistics data for complete picture

• Reports that are fully configurable by the user - build your own dashboard to track your trial progress• Automated alerts to your desktop• All in real time

QUALITYCenduit’s focus

• 21CFR Part 11-compliant• Fully validated system build process• Built-in Quality Assurance• Routine, automated data checks

throughout trial process• A Quality First culture

Ha

pp

ier Site

s

CLINICAL SUPPLIESCenduit optimizes the use of all available materials

• Control of release through integration with GMP inventory

• Control of multiple storage facility inventories in global trials

• Control of expiry dates• Pooling of study medication• Management of ancillary materials and lab kits• Visibility of cold chain supplies

- Tracking to kit level

ACCESS TO EXPERTISECenduit project management

• U.S. and European project management offices established 10 years

• Consultation on trial design and system solutions

• 24/7 Helpdesk• Multilanguage capability

HAPPIER SITES.

We know that what matters most is our ability to make sites feel confident and in control, which leads to improved protocol compliance, less wastage and better site performance. Don’t rely on trial and error. Conduct smoother, happier trials with Cenduit.

EASE OF USE FOR INVESTIGATOR SITESCenduit’s interactive response technology

• Web access with phone backup• Drug logistics management• Patient screening, randomization

and visit management• Patient drug assignment

• Treatment unblinding• Drug accountability and

returns management• Integration with EDC• Study simulation and forecasting

Sma

rter So

lutio

ns

THERAPEUTIC EXPERTISE • Anti-Inflammatory• Asthma• Bone Diseases• Cardiovascular• Central Nervous System• Diabetes• Endocrinology• Immunology & Infectious Diseases• Metabolic Diseases• Nephrology• Oncology• Pain • Pediatrics• Psychiatric Disorders• Respiratory & Pulmonary • Rheumatology

STUDY-SPECIFIC EXPERTISE• Phase I-IV• Complex Dosing• Vaccines• Biosimilars• Investigator-Led• Complex Randomization Designs• Open Label

SMARTER SOLUTIONS, SMOOTHER STUDIES & COMPLETE CONTROL.

Conducting a clinical trial is complicated enough without having to deal with problems and setbacks. With Cenduit you can focus on your trials, not tribulations.

Whether you are developing a vaccine or a biotech product, or running an early-phase or late-phase study, we will design a smart process and a smart system tailored to the needs of your trial. Our unique combination of clinical operations and clinical supplies expertise and our study-specific approach to project management will help you ensure seamless patient enrollment, randomization and drug supply management.

CLINICAL INTELLIGENCECenduit’s reporting module

• Intelligent reports that provide useful information for decision making

• Integration with EDC, labs and logistics data for complete picture

• Reports that are fully configurable by the user - build your own dashboard to track your trial progress• Automated alerts to your desktop• All in real time

QUALITYCenduit’s focus

• 21CFR Part 11-compliant• Fully validated system build process• Built-in Quality Assurance• Routine, automated data checks

throughout trial process• A Quality First culture

Ha

pp

ier Site

sCLINICAL SUPPLIESCenduit optimizes the use of all available materials

• Control of release through integration with GMP inventory

• Control of multiple storage facility inventories in global trials

• Control of expiry dates• Pooling of study medication• Management of ancillary materials and lab kits• Visibility of cold chain supplies

- Tracking to kit level

ACCESS TO EXPERTISECenduit project management

• U.S. and European project management offices established 10 years

• Consultation on trial design and system solutions

• 24/7 Helpdesk• Multilanguage capability

HAPPIER SITES.

We know that what matters most is our ability to make sites feel confident and in control, which leads to improved protocol compliance, less wastage and better site performance. Don’t rely on trial and error. Conduct smoother, happier trials with Cenduit.

EASE OF USE FOR INVESTIGATOR SITESCenduit’s interactive response technology

• Web access with phone backup• Drug logistics management• Patient screening, randomization

and visit management• Patient drug assignment

• Treatment unblinding• Drug accountability and

returns management• Integration with EDC• Study simulation and forecasting

Sma

rter So

lutio

ns

THERAPEUTIC EXPERTISE • Anti-Inflammatory• Asthma• Bone Diseases• Cardiovascular• Central Nervous System• Diabetes• Endocrinology• Immunology & Infectious Diseases• Metabolic Diseases• Nephrology• Oncology• Pain • Pediatrics• Psychiatric Disorders• Respiratory & Pulmonary • Rheumatology

STUDY-SPECIFIC EXPERTISE• Phase I-IV• Complex Dosing• Vaccines• Biosimilars• Investigator-Led• Complex Randomization Designs• Open Label

EVERY PATIENT. ON TIME. EVERY TIME.

There is no room for error when randomizing patients and assigning them treatment. For this reason, quality assurance is at the foundation of everything we do. We will always randomize patients into the right treatment group, we will always assign them the correct medication, and we will always ensure that the medication is available for them every time they need it.

Our quality procedures include oversight of the entire IRT system setup and validation process as well as ongoing statistical monitoring of all studies to ensure absolute clinical protocol compliance.

We help our sponsors take control of their trials while eliminating the tribulations. That is Cenduit’s commitment to quality and to the success of your trial.

Every Pa

tien

t. On

Time. Eve

ry Time.

Randomization of the patient into the correct treatment group

Assignment of the correct medication to the patient

Availability of the medication at the clinical site when the patient needs it

CENDUIT’S QUALITY COMMITMENTCenduit helps its sponsors control the most important elements in a clinical trial:

+1 919.998.3860

RFP@cenduit.com

www.cenduit.com

Global Sales and Marketing

THE CENDUIT PATH TO PATIENT DRUG COMPLIANCE IN YOUR CLINICAL TRIALS