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Results!
by Sylogent Sylogent is a team of professionals that work diligently each day to solve problems and deliver results. We view each problem as an opportunity to help our clients achieve and exceed their goals. Below is a partial list of results we have delivered to the pharmaceutical marketplace.
Customized Corporate Disclosure & Transparency
Cheaper Clinical Study Reports
Clinical Trial Results Disclosure
Creating Great Protocols
Protocol Writer is an easy-to-use electronic template that helps standardize your protocol design and maximizes the reuse of protocol design data in downstream processes. The integrated rules engine contains critical regulatory validation that must be taken into consideration when writing a protocol. For example, the rule engine includes the validation that will take place with the new clinical data disclosure regulations for ClinicalTrials.gov, EudraCT and other international registries. Successful pharmaceutical companies must consider how protocol data will be used and viewed on disclosure registries.
The Protocol Writer is one of many electronic forms that can reside in your customized FormPharm that is hosted by Sylogent. FormPharm is a web-based portal that hosts and shares data between all your clinical development form templates.
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Registering Your Protocols
VCTR is a proven protocol registration and clinical trial results disclosure solution that has been in production since 2005. The system was designed to greatly reduce the cost, resources and time required to stay compliant with the rapidly changing registry disclosure process. VCTR integrates all the compliance requirements based on current legislation to help ensure that your clinical data in the public domain is accurately disclosed.
Simplify the protocol registration process
Minimize internal resources and budget needs
Configure to maximize workflow and process efficiencies
Ensure compliance with all corporate and international registries
Automate data entry via XML data feeds or Excel template uploads
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Smarter Patient Recruiting
Our patient screening tools and services are designed to help draw and retain patients and investigators for your clinical trials. By leveraging our vast experience with protocol registration and patient recruiting, we are able to help you attract the right patients or investigators at the lowest cost. Tools include corporate registries such as amgentrials.com, rochetrials.com or gsk-clinicalstudyregister.com. Our services also include study-specific screeners that can be placed on international or client registries.
Build opt-in patient and investigator database
Leverage disclosed protocol on international or client registries
Create patient-friendly recruiting summaries
Maximize protocol registration regulation and process
Reduce patient recruiting budgets
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Customized Corporate Disclosure & Transparency
The Client Registry is an invaluable tool for those pharmaceutical companies seeking to remain compliant with new disclosure regulations, optimize patient or investigator recruiting and maximize a positive corporate image. Clients can post protocols, patient trial screeners, clinical trial results data, results summaries, investigator surveys, investigator payments and other corporate information that must be disclosed to the public.
Maximize recruiting and study exposure
Meet or exceed disclosure compliance regulations
Efficiently recruit patients and study investigators
Optimize image with patients, investigators, investors and regulators
Simplify recruiting process
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Cheaper Clinical Study Reports
The Clinical Study Report(CSR) Generator is an easy-to-use web-based template that helps standardize and simplify your CSR creation process. The CSR generator is integrated on the SylogiQ platform so it leverages data from up-stream processes. You now can run your clinical trial disclosure, CSR creation and publication planning efforts in parallel which is guaranteed to save time, money and resources.
Reuse data from up-stream processes
Standardize and optimize CSR process
Save time, resources and money
Utilize outsourced lower-cost resources to create CSR shells
Flow CSR data to data disclosure templates
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Clinical Trial Results Disclosure
VCTR is the leading protocol registration and clinical trial results disclosure solution that has been in production since 2005. The system was designed to greatly reduce the cost, resources and time required to stay compliant with the rapidly changing registry disclosure process. VCTR integrates all the compliance requirements based on current legislation to help ensure that your clinical data in the public domain is accurately disclosed.
Simplify the clinical trial results disclosure process
Minimize internal resources and budget needs
Configure to maximize workflow and process efficiencies
Ensure compliance with all corporate and international registries
Automate data entry via XML data feeds or Excel template uploads
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Automate Publication Manuscripts
PubSTRAT streamlines the manuscript review and approval process from early stage planning through final submission. PubSTRAT also facilitates collaboration between all stakeholders and provides visibility and transparency into the entire process. This flexible and configurable application allows your organization to easily modify processes, and alerts team members as your requirements evolve. PubSTRAT is available in modules or as an all inclusive suite of products.
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Journal Selector
Journal Selector is the industry's leading database to all of the best peer-reviewed biomedical journals. All the information you need is easy to access so that you can quickly identify the right journals for your publications.
Instant access to all of the best journal profiles
Easy search and robust filtering capabilities guide you to your optimal target
Improve targeting and shorten time to publication
Search by Therapy, Topic or Title
Create favorites and save key contacts
NEW Audience Browse!
For more information please visit journalselector.com
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Conference Authority
Conference Authority is the industry leading database to all of the best medical conferences. All the information that you need is easy to access so that you can quickly identify the right conferences for your abstracts and sponsorship opportunities.
Instant access to all of the best conference profiles
Easy search to find your optimal target
Intelligent and proprietary data input process
Create favorites and save key contacts
Conference database update every day
Optional access to Journal Selector database
Journal Selector
CiteCentral
For more information please visit conferenceauthority.com/
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CITE CENTRAL
Cite Central is a single repository solution that provides 24/7 access to all your citations, manuscripts and bibliographies. Easily search by key words or document text. Cite Central is also a great place to store all your important team documents and product or team news. .
Easy 24/7 access to all presented publications and presentations
Intelligent smart search feature for fast retrieval
Interactive news and activities section
Simple intuitive navigation
Full team and company wide access
For more information please visit citecentral.com
eKnowledge Management
The Knowledge Repository is a modular repository solution that provides 24/7 access to all your company or team documents. The full text search capabilities allow you to quickly locate specific documents with the push of a button. The Knowledge Repository can also be configured to easily pass approved data or documents to other systems.
Simple user interface for quick document retrieval
Automated aggregation of approved data and documents
Configurable access for data and document control
Easily integrate with other systems
Confident archiving and retention system
Enterprise scalability
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Virtual + Mobile Approvals
The Approvals Module is a configurable application created to simplify, standardize and streamline the corporate approval process. You can now manage, review and approve all internal and external disclosure requests from a single interface. The module also includes a mobile version for your smartphone so that you can review and approve while on the move!
Simple task-based system for all executive disclosure approvals
Configurable Decision Matrix for easy form and workflow selection
Unlimited forms and workflow configuration
Confident archiving and retention system
Enterprise scalability
Smartphone component for mobile approvals
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