Portico

Clinical portal development framework

Portico. Clinical portal development framework

The choice of industry leaders

Clinical organisations, regardless of size, continue to evolve and optimise their online strategy to drive engagement, differentiation and create real competitive advantage. The Portico clinical portal development software framework, is the public face of a growing number of leading clinical companies worldwide. In conjunction with our experienced management, compliance, operational and engineering teams, the Portico framework will enable you to design and deliver a customer-centric and information-rich online portal that combines content, data and regulatory documents in a right-sized, secure and compliant solution.

Comprehensive and proven Clinical features 

Reduced cost and time to market

Whether you're on SAP, Oracle / JD Edwards, Sage or any of the other leading ERP and billing systems, Portico will externalise your clinical trial and commercial data to your customers on your terms.  Portico ensures your portal development project is quick, secure and cost effective.

Examples features include:

- Stock and Inventory reports
- Blinded & Un-blinded controls
- Order entry
- Depot reports
- Usage Analytics
- Real-time Track+Trace
- Email alerting framework
- User registration
– User and Group-based roles
– Document generation

Portico features highlights

Comprehensive capabilities out of the box.

ColdTrack is the most flexible, scalable and technologically advanced shipment monitoring technology available on the market today – designed and built with the latest technology to the latest standards to  deliver instant visibility of temperature-sensitive clinical assets on the move globally.

Stock and Inventory reports

Blinded and Unblinded Clinical trial controls

Project and role-based document repositories

3rd party Courier
depot reports

Access reports and usage analytics

Temperature-sensitive track and trace

User and Group-based Roles

Group and user level roles and security levels

Document and report creation

Pre-packaged courier data feeds

Overview

Portico has integrated support for inventory and transit reports from the leading shipment providers.  

We have done all the hard work so you don't have to.

Examples include:

Integrate custom feeds or choose from from our existing reports including:

World Courier
- Per site / per depot
- Shipment tracking reports

Create Documents and Reports - Fast!

Template-driven document design

With Portico's integrated  document generation tools, you can quickly and easily add document creation and reporting to your clinical portal applications.

Multiple file formats supported

Supports output formats:
- Word .doc and .docx
- PDF
- HTML
- ODT
– RTF

Supports Desktop and Mobile devices

Web.

Portico is powered by modular building blocks, delivering the functionality you need and combining it into completely new web-enabled applications. Our building blocks are incredibly flexible; they can be reused across multiple devices and combined to deliver a more engaging online experience.

Mobile.

Mobile apps are an increasingly important way to differentiate your services and build end-user relationships that will win hearts and minds. Meeting your customers wherever they choose to be and delivering an outstanding customer experience is crucial to competitive advantage.

Built on industry-standard architectures

RESTful APIs

Portico is powered by modular building blocks, delivering the functionality you need and combining it into completely new web-enabled applications. Our building blocks are incredibly flexible; they can be reused across multiple devices and combined to deliver a more engaging online experience.

Mobile.

Mobile apps are an increasingly important way to differentiate your services and build end-user relationships that will win hearts and minds. Meeting your customers wherever they choose to be and delivering an outstanding customer experience is crucial to competitive advantage.

Scope. Scale. Compliance. 

Scope.

All technology projects have two primary areas for complexity - Technical scope and Business scope.  The technical scope centers on building the desired product; Management scope includes the business aspects of the project, staff, relationships and project organization. Managing these issues is a key function of our experienced and knowledgeable team.

Scale.

Long-term success demands a real understanding of the scale of any project . Scale is one of the keys to successful delivery, accounting for right-sized scope, right-sized services, technology decisions and documentation needs. Our breadth of experience working with the smallest of Biotech start-up to Top-10 pharma allows us to scale you requirements to meet demands.

Compliance.

Our solutions are designed from the outset to enable Clinical to collect, manage and report clinical trial data in full compliance with global regulations and guidance. Our compliance spectrum includes:
FDA 21 CFR Part 11
GxP including the cGMPs
GAMP-5
EU Annex 11

Regulatory compliance 

Regulations assessed throughout the development life cycle

This is a subset of the regulatory obligations that our technology is designed to meet. We also provide support during the requirements definition, URS development and validation phases. Our partners can perform regulatory reviews and science-based risk assessments to ensure your systems maintain compliance. These validation processes are based on FDA and PIC/S guidance.

Good Clinical Practice – MHRA Good Clinical Practice Guide

Good Manufacturing Practice (GMP)
 
 - FDA 21 CFR Part 11 (and predicate rules) 
 - EudraLex Volume 4 Annex 11 
 - EudraLex Volume 4 Chapter 4 

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