PPD DirectConnect

Technology Services

For more information on PPD's specific technology services, please choose an option from the drop-down box below.

 

Client Portals - PPD DirectConnectâ„¢

As one of the first in the industry to pioneer secure Web portals, PPD gives our biopharmaceutical and medical device clients 24 hours a day, seven days a week access to information and progress reports on clinical trials being performed on their behalf by PPD.

Developed in close collaboration with companies across the industry, PPD has refined this secure and efficient study communication and management tool to be used in projects with diverse needs. Today, PPD hosts thousands of users for more than 125 biopharmaceutical, government and and medical device clients.

PPD DirectConnect provides a secure, centralized source of information for efficient management of your clinical trials. The technology is browser neutral and requires no plug-ins or downloads, other than the use of Adobe Acrobat reader for PDF documents.

Leveraging the PPD DirectConnect architecture, PPD has developed customized, branded Web portals for large scale programs, providing program management utilities, study information, status reports and a single point of access to tools such as remote data entry. Role-based access can be implemented to further customize the experience. Our developers are skilled at adding unique functionality per the needs of each program.

Clinical Trial Website Security

We host each of your clinical trial websites on servers dedicated to sponsor sites and are located securely behind PPD firewalls. Using server-based security, each site requires authorization and authentication of anyone trying to access and encryption for all transactions and communication between user and site. Further, password administration is governed by procedures that are strictly defined and monitored for optimal security.

Centralized Source of Clinical Trial Information

PPD DirectConnect supports timely and efficient management and communications for your clinical trials by combining key functional elements:

  • Project team communications - contact information and e-mail links for project team members; meeting calendars, agendas and minutes
  • Document repository - key project documents such as protocols, CRFs, review guidelines and relevant sections of the master action plan
  • Project status reports - reports from our clinical trial management system, our query resolution system, an interactive voice response system, data management reports, pharmacovigilance reports and the LiveLink Imaging System, as well as ad hoc or customized reports developed by the project team to your specifications
  • Deliverables - draft electronic deliverables such as biostatistics tables and listings and medical/regulatory reports, with capability for electronic data and file transfers
  • Administrative information - contracts, SOPs and other documents supporting the sponsor/PPD partnership
  • Special features - customized capabilities, such as limited access to tools (remote data access, limited access to sites/investigators for study information or links to other relevant Web resources)

Whether you are a current PPD client or considering using our services in the future, PPD DirectConnect is an easily added tool to any project. For more information on what a PPD DirectConnect site can do for your clinical, contact us.

 

Electronic Data Capture (EDC) | Clinical Trial Electronic Submissions |

IVR and IWR Systems | IVR and IWR System Services |

Adverse Event Adjudication | Clinical Trial Software Consulting |

Clinical Trial Software Products | Clinical Trial Safety Reporting |

Client Portals - PPD DirectConnectâ„¢


 

Dr. Martin Lee discusses the importance of feasibility studies and the steps involved in designing and conducting them in a video