Presented by
IPI Academy
How to Advance and Accelerate Clinical Trials Training Course
This course has been specifically designed to review ways to accelerate the clinical trial process and will provide an excellent opportunity to discuss the opportunities available and how to implement them with an expert in the field of pharmaceutical business development.
7 December 2023
from £549
- Format: Live online
- CPD: 6 hours for your records
- Certificate of completion
- Clinical Quality Management Systems
- Clinical Trial Regulatory Requirements
- EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience
- GCP and Clinical Research Update - Hot Inspection Topics
- Managing Vendor/CRO/CMO Oversight
- Update - Latest Position on the New UK Clinical Trial Proposals
- How to Advance and Accelerate Clinical Trials
Overview
Clinical trials are prospective biomedical or behavioural research studies on human participants, designed to measure interventions related to new treatments to warrant further investigation. There are four types of clinical trials:
- Pilot studies and feasibility studies
- Prevention trials
- Screening trials
- Multi-arm multi-stage (MAMS) trials
Clinical trials look to prevent, detect and/or treat disease. The goal of a clinical evaluation programme is to determine the efficacy and safety of a potential new drug compound. Invariably clinical trials are time-consuming and heavily influenced by a series of manual interventions which are designed into the study enrolment, set up and protocol execution document.
The course will address options to consider ways to speed up the clinical trial process with emerging technologies, utilising smart packaging and software automation tools, such as artificial intelligence (AI). It will also review the advantages of being adaptive to work with different business models ie: decentralised clinical trials, direct-to-the-home and/or a hybrid combination of home/clinic.
This course has been specifically designed to review ways to accelerate the clinical trial process and will provide an excellent opportunity to discuss the opportunities available and how to implement them with an expert in the field of pharmaceutical business development.
Benefits of Attending
- Share, learn and discuss information on emerging technologies for clinical trial application
- Hear recommendations for consideration
- Challenge the status quo
- Learn how to improve the timeline of setting up a clinical study
- Boost patient outcomes and reduce the timeline for drug approval
- Gain a tangible competitive advantage, return on investment (ROI)
- Drive innovation and improvement within your organisation
Who Should Attend
Pharmaceutical companies, emerging Biotech enterprises and Contract Research Organisations.
Personnel in the following roles and departments:
- VP Clinical Operations
- VP Digital Strategy
- Clinical Administration
- Clinical Research Assistants
- IT
- Data Management
- Financial Director/Manager
- Patient Advocate
- Head of Procurement
- Project Team Managers
- Business Development Managers
The How to Advance and Accelerate Clinical Trials course will cover:
Welcome and Introduction
Defining a Coherent Patient Recruitment Strategy
- Choosing the right marketing mix and vendor profile
- Working with specialist digital providers to improve the process
Identifying “Active” Real-World Patient Groups Pre-Screened and Ready for Enrolment
- Sourcing active patient data
- Speeding up the enrolment and study set-up time
Utilisation of a Clinical Trial Feasibility Tool
- Taking early decisions to make the right long-term choice regarding the demographic reach for each study
- Working with data analytics to drive the decision-making process
Boosting Patient Engagement and Retention Rates via an Automated SaaS Payment Fulfilment System - Milestone Based
- Take away the upfront financial burden for a patient
- Consider a patient-centric approach to boost the engagement and retention of patients when using fintech payment technology
Supporting the Patient Journey
- Provide a global (digital) concierge service which enables a patient to travel to a clinic
- No out-of-pocket expense incurred
Enhancing your Relationship with Site(s) via an Intuitive Automated Payment System
- Better relationships can deliver better support loyalty and overall performance
- Work with sites to create a win/win collaboration agreement
Providing Accurate and Real-Time Visibility of Patient Compliance, when Engaged in a Study via Remote Patient Monitoring (RPM)
- RPM software/hardware can provide critical data points relating to patient compliance rates
- An integrated digitalized approach to compliance can help drive up the efficacy and accuracy of reporting contained within a clinical study protocol
Adoption of a Digitalised Electronic Investigational Site File (eISF)
- Adoption of new, SaaS software can help to improve the manual labour cost and speed up the documentation process related to an investigational (quality management) site file
Shared Experience, Learning and Future Actions
Graham Howieson
GH Consutling
Graham Howieson is a pharmaceutical business development consultant, inventor and entrepreneur. He is a highly experienced and competent leader, with an International pedigree covering UK, EU, USA and Asia. An industry pioneer with a forward thinking approach to design and the delivery of new innovative drug delivery and smart packaging solutions for over twenty five years. Worked extensively and exclusively within the pharmaceutical space with leading global enterprises such as: Glaxo Smith Kline, Astra Zeneca, Johnson and Johnson, Sanofi . Building value by solving technical, engineering, regulatory, compliance and brand communication related issues. Working to fulfil a client brief, in terms of the budget, timeline, return on investment for commercial use.
Alongside he has acquired a range of specialist skills which encompass the development of new, emerging technologies to improve the delivery of clinical trials , areas of interest include: intellectual property, digital engagement, bespoke software, SaaS, automation, AI, machine learning, remote compliance monitoring, patient engagement/retention, omni-channel communication, wearables, video enablement tools, VR, hybrid and virtual (supply chain) modelling. The primary objective with all technological advances is to achieve process improvement and increased speed of delivery, aligned with a multi-sensory patient experience.
Book How to Advance and Accelerate Clinical Trials Live online training
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
- 30% off the 2nd delegate*
- 40% off the 3rd delegate*
- 50% off the 4th delegate*
Please contact us for pricing if you are interested in booking 5 or more delegates
7 December 2023
Live online
09:00-17:00 UK (London) (UTC+00)
10:00-18:00 Paris (UTC+01)
04:00-12:00 New York (UTC-05)
Course code 14246
- GBP 549 649
- EUR 789 929
- USD 893 1,049
Until 02 Nov
- 1 day live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price.
