Onorach Clinical is a clinical research organization headquartered in Dundee, Scotland that manages clinical trials from Phase I-IV. It has locations also in Latvia and provides services to pharmaceutical and medical device companies of all sizes. Onorach focuses on innovative electronic solutions to improve clinical trial quality and efficiency. It has expertise across many therapeutic areas including oncology, diabetes, vaccines, and more. Onorach aims to deliver high-quality, cost-effective clinical trial services through strategic partnerships.
CHC15 - EHR adoption in a european environment and public management hospital...Carlos Sousa
SOURCE:
Invited speaker for CERNER HEALTH CONFERENCE, Educational Session, held during Oct 11-14 in Kansas City (MO) - US.
ABSTRACT:
After 13 years under private management, Hospital Prof. Fernando da Fonseca (HFF) committed to invest a solid EHR strategic approach aligned with best practices, due to management shift as public management hospital within the NHS network. HFF focused on creating a Clinical Commission for information that could support and lead the change on workflow and mindset of the hospital culture. This team combines the knowledge and experience of multidisciplinary roles, designing a EHR model that fully responds to the needs. Thus ensuring a successful phased implementation which started in the emergency department and was then deployed throughout the rest of the hospital. After three years of project, the hospital has achieved a high level (superior to 85%) of EHR adoption and has proven outcomes in the delivery of quality of care and Social ROI (e.g. direct data interoperability with medical emergency before hospital admission, algorithm implementation to improve organ donor and collection, integration with private clinics for outsourcing auxiliary services, including Lab and radiology prescriptions and results/reports). HFF continues to strongly work on this project and are dedicated to implementing their roadmap with the short term aim of achieving HIMSS Stage 6.
In this PPt contain the E6 R1 and E6 R2 information , and the GCP training material for the Good prectice. and end of the ppt there is a ink which is use for your online training and generate certificate.
The Medical Affairs team at GVK Biosciences (GVK BIO) comprises of well trained medical professionals with cumulative Clinical Research experience of about 28 years.
Presentation exploring the development of clinical trial registries and clinical trial results databases and their impact on the clinical study industry, including their challenges and the potential for creating new forms of liability.
POINT-of-IMPACT testing. A European perspective - Bert NiestersWAidid
At SoGat meeting 2019 Bert Niesters - Professor in Molecular Diagnostic in Clinical Virology, Medical Molecular Microbiologist at University Medical Center Groningen, Department of Medical Microbiology, Division of Clinical Viroloy, The Netherlands - has talked about the developing trends in molecular diagnostics and the impact on the Laboratory.
To learn more, please visit www.waidid.org!
July 27, 2007 presentation to the USC Regulatory Affairs Masters program, with a focus on:
* The Evolution of Demand for Clinical Trial Registries
* Review of Key National and International Registries
* Challenges of Registries and Databases
* Developments to Watch on Clinical Trial Registries
Clinical Trial Opportunities in Russia and Eastern Europe - Raising the VeilJulia Kondakov
Natalia Nayanova, Director of Clinical Operations and General Director of the Russian Headquarters, gave a presentation explaining tremendous opportunities for conducting clinical trials in Russia, Eastern Europe, and CIS revealing myths and realities on the subject, and described Accell’s ample experience on the market.
Nordic Life Science Days,
Stockholm, Sweden
September 14-15, 2016
CHC15 - EHR adoption in a european environment and public management hospital...Carlos Sousa
SOURCE:
Invited speaker for CERNER HEALTH CONFERENCE, Educational Session, held during Oct 11-14 in Kansas City (MO) - US.
ABSTRACT:
After 13 years under private management, Hospital Prof. Fernando da Fonseca (HFF) committed to invest a solid EHR strategic approach aligned with best practices, due to management shift as public management hospital within the NHS network. HFF focused on creating a Clinical Commission for information that could support and lead the change on workflow and mindset of the hospital culture. This team combines the knowledge and experience of multidisciplinary roles, designing a EHR model that fully responds to the needs. Thus ensuring a successful phased implementation which started in the emergency department and was then deployed throughout the rest of the hospital. After three years of project, the hospital has achieved a high level (superior to 85%) of EHR adoption and has proven outcomes in the delivery of quality of care and Social ROI (e.g. direct data interoperability with medical emergency before hospital admission, algorithm implementation to improve organ donor and collection, integration with private clinics for outsourcing auxiliary services, including Lab and radiology prescriptions and results/reports). HFF continues to strongly work on this project and are dedicated to implementing their roadmap with the short term aim of achieving HIMSS Stage 6.
In this PPt contain the E6 R1 and E6 R2 information , and the GCP training material for the Good prectice. and end of the ppt there is a ink which is use for your online training and generate certificate.
The Medical Affairs team at GVK Biosciences (GVK BIO) comprises of well trained medical professionals with cumulative Clinical Research experience of about 28 years.
Presentation exploring the development of clinical trial registries and clinical trial results databases and their impact on the clinical study industry, including their challenges and the potential for creating new forms of liability.
POINT-of-IMPACT testing. A European perspective - Bert NiestersWAidid
At SoGat meeting 2019 Bert Niesters - Professor in Molecular Diagnostic in Clinical Virology, Medical Molecular Microbiologist at University Medical Center Groningen, Department of Medical Microbiology, Division of Clinical Viroloy, The Netherlands - has talked about the developing trends in molecular diagnostics and the impact on the Laboratory.
To learn more, please visit www.waidid.org!
July 27, 2007 presentation to the USC Regulatory Affairs Masters program, with a focus on:
* The Evolution of Demand for Clinical Trial Registries
* Review of Key National and International Registries
* Challenges of Registries and Databases
* Developments to Watch on Clinical Trial Registries
Clinical Trial Opportunities in Russia and Eastern Europe - Raising the VeilJulia Kondakov
Natalia Nayanova, Director of Clinical Operations and General Director of the Russian Headquarters, gave a presentation explaining tremendous opportunities for conducting clinical trials in Russia, Eastern Europe, and CIS revealing myths and realities on the subject, and described Accell’s ample experience on the market.
Nordic Life Science Days,
Stockholm, Sweden
September 14-15, 2016
Oncology Dynamics captures a substantial part of oncological patient treatment journey. It provides real world insights into how standards of care and treatment landscape differ across healthcare systems.
Crystal Research Associates, LLC has initiated coverage on SpectraScience, Inc. (SCIE-OTC) with the release of a 48-page Executive Informational Overview.
Clinical Research Organization Services | Contract Research Company - PepgraPEPGRA Healthcare
Pepgra is a global contract research organization and drug development services company. It provides various phases of clinical research trials services to pharmaceutical and biotechnology companies to help reduce the time and costs associated with drug development.
Contact Us:
Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
India: +91 9884350006
United Kingdom: +44- 74248 10299
ECO 11: Medicines Optimisation in Northern Ireland - Frans van AndelInnovation Agency
Frans introduces the work of the Medicines Optimisation Innovation Centre based in Northern Ireland. He talks about their background; aims and how they achieve them; and current key initiatives. Frans also discusses the ongoing work of MOIC in enabling technology, the pharmaceutical industry, knowledge transfer, training and education, and other key initiatives.
Customized Oncology Development Solutions: Clinical Trials Designed Around You®Covance
Oncology is one of the most research-intensive therapeutic areas, yet no two development programs are the same. No two trials are the same. Each one calls for a customized strategy and distinct trial management approach. Covance develops fit-for-purpose solutions Designed Around You® that enable more efficient clinical trials and focus on what is most valuable to your organization.
Outlining the proces and lessons learned in organising the technological infrastructure at the Radboud university medical center, to shape the Radboudumc Technology Centers, supporting our mission in enabling personalized healthcare.
Jane Blower, Deputy Chief Scientific Officer (Acting) NHS England. Jane's presentation from the Seven Day Services event in the East Midlands on 12th June 2014.
Similar to Onorach Clinical; Onorach Baltics; Onorach Innovation ceating disruptive services and technologies to improve clinical trial outcomes. (20)
5. What we do
Onorach®
Clinical manage Phase I to IV clinical
research studies for drug products (including
biologicals (stem cells)) and medical devices using a
tailored partnership approach that provides an
effective and efficient route for clients and patients to
benefit from the potential of their products.
Onorach®
provide pharma companies (from emerging,
virtual and SMEs to large-scale multinationals) with a
responsive and flexible development service.
6. Locations
• Onorach Clinical founded in 2009
• Onorach Innovations founded in 2015
• Both headquartered in Dundee, Scotland UK
• Onorach Baltics, based in Riga Latvia founded in 2015
• Onorach group capable of managing Clinical Trials in over
26 countries
Riga
Dundee
(Headquarters)
United
Kingdom Latvia
7. What sets us apart
“Onorach®
have developed a range of transformational services
that completely change the success rate of patient recruitment
and retention in clinical trials.
Stephen Leiper, CEO
8. What sets us apart
Onorach was created following research conducted into CROs performance in the industry.
The research identified 5 areas where clients felt CROs under-delivered.
Onorach has developed a philosophy of eDIB (electronically doing it better) which is a suite of
electronic solutions that together improve the quality of data in Clinical Trials:
9. What sets us apart
Client time/resources
required to manage project
Current industry model
10. What sets us apart
Client time/resources
required to manage project
Onorach®
innovative model
11. What sets us apart
• Onorach’s business model has been designed directly in response to client
requests for a holistic approach to delivery of clinical trial services. Existing
and potential partners are very attracted to this concept, and Onorach is able
to select high quality partners based on their expertise and ability to add value
in delivering a cost effective solution on time and within budget.
• Onorach® work with companies of any scale from virtual to multi-
national. The Company has developed niche markets in dentistry, health and
well-being and investigator led (non-commercially funded) clinical trials.
• Onorach® is led by Professor Christene Leiper who’s 30 year’s hands-on
experience within the health industry is unusual. It is a huge benefit for a CRO
to have a managing director with these credentials. Professor Leiper has a
global reputation in a variety of therapeutic areas, which is greatly
appreciated by potential clients, as she fully understands their opportunities
and challenges.
12. Service areas:
GCP compliant Clinical Trial Management:
• Clinical research which is bespoke i.e. “turn-key” or special requirements
• Communication, planning & development
• Gap Analysis & Risk Management
• Clinical Operations Management
• Protocol design in collaboration with clients
• Site set-up, site initiation, patient recruitment
• PI selection
• Monitoring
• Medical Report Writing
• Data capture, storage, management and statistical analysis
• Regulatory and Quality management
• Site Close-out
• Stability & Palatability Studies
• Clinical Trial Supplies
13. Therapeutic areas:
• Central Nervous System
• Diabetes
• Respiratory
• Oncology
• Hepatology/Gastroenterology
• Stem Cells
• Paediatrics/Neonatal Intensive Care
• Vaccines
• Renal Impairment
• Medical Devices
• Haemophilia
• Cardiology
• Other
14. Cardiovascular capabilities in CVD
Expertise:
•Noninvasive imaging including nuclear perfusion studies, cardiac computed
tomography(CT), Cardiac Magnetic resonance imaging(CMRI), Cardiac Positron Emission
Tomography(PET) and Echocardiography-either in Dundee or Latvia
•GradCed exercise testing
•Flow mediated dilation
•Platelet Aggregation
•Ambulatory blood pressure monitoring
•ECG studies demonstrates thorough understanding of dosing requirements, study
design, conduct and study-group sizes
•Full suite of service offerings including protocol development, clinic conduct, ECG
analysis, data management, fully integrated statistical analysis, study reports, regulatory
submission support and ECG
These integrated services ensure production of the highest-quality data, turn-key
operations and process efficiencies, which result in cost savings
15. Paediatrics/Neonatal Intensive Care
Expertise:
• Extensive paediatric clinical diagnostic and research experience including
paediatric imaging in Nuclear Medicine
• Knowledge of clinical trials examining various drugs used in paediatrics
• Active member of NeoCirc clinical trial phase III study on the use of dobutamine
with neonates
Capabilities:
• Onorach® have access to some of the best NIC and Paediatric research units
internationally
• We have strong links to international experts in paediatric/neonatal intensive care
(including key authorities for PIP & PUMA guidelines)
16. Haemophilia
Expertise:
• Post-marketing safety study following the treatment of subjects suffering with
severe haemophilia A involving the collection of safety data in an EU country
including inhibitor development, unexpected adverse drug reactions and serious
adverse drug reactions.
• Onorach team has experience in haemophilia and aphoresis treatments.
Capabilities:
• We can manage haemophilia studies at UK and international hospitals and have
access to industry experts. (eg. a QP specialising blood bank experience)
17. Hepatology/Gastroenterology
Expertise:
• Acted as UK Medical Liaison for a German hepatology company and conducted
CTs with several London hospitals
• Clinical trials included HIV co-infection and IgG4-associated Cholangitis, Acute on
Chronic liver failure and various gastroenterology studies
Capabilities:
• We can manage hepatology/gastroenterology studies in the UK and
internationally and have access to relevant diagnostic equipment
• We have access to both leading UK experts in hepatology as well as
other international opinion leaders
• Strong relationship with the editors of ‘GUTS Journal’ for gastroenterologists
18. Oncology
Expertise:
• Clinical and research experience, including project management for end-of-life
patients and telemedicine for remote areas
• Various research experience across chemotherapy, solid tumors, retrospective
studies and patient’s ‘quality of life’ studies
Capabilities:
• We can manage oncology research projects at key UK & international sites
(including haematalogical cancers) and have access to diagnostic medical
imaging, ultrasound and biomarker technologies.
• Onorach are building a specialist Oncology Clinical Trials unit in Latvia
• We have access to key opinion leaders internationally across 26 countries
19. Diabetes
Expertise:
• Experience of diagnostic & clinical research. Worked on medications for diabetes
mellitus types I & II.
• Research into peripheral neuropathy, glucose testing medical devices, retinal
detachment and sliding scale insulin studies
• Experience of blood glucose monitoring devices
Capabilities:
• There are strong diabetes research networks across both Scotland and England
• Global coverage for diabetes studies & diagnostic medical imaging
• Glucose clamp technique (quantifying insulin secretion & resistance)
• We have access to key opinion leaders at Aberdeen Royal Infirmary, Ninewells
Dundee & Edinburgh Royal Infirmary (amongst others)
20. Central Nervous System
Expertise:
• Written 1st
Scottish standards for stroke admissions & rapid treatment
• Experience of CT for Alzheimer’s, Parkinson’s, Huntingdon’s, Multiple Sclerosis &
various neurological tumours
• Experience of CNS studies
Capabilities:
• Global coverage for CNS studies
• Access medical imaging for CNS diagnostic/research studies
• We have access to key opinion leaders at Aberdeen Royal Infirmary & Edinburgh
Royal Infirmary (amongst others)
21. Respiratory
Expertise:
• PhD in respiratory medicine (specialising in pulmonary embolism, COPD & chronic
lung infections). Performed many clinical trials on respiratory diseases including
NSAIDS, bronchiolitis, COPD, cystic fibrosis etc.
• Published author 2011, Respiratory – Positive Ventilation Delivery Systems.
• Experience of research into COPD
Capabilities:
• We can manage respiratory research projects across 26 countries and have access
to diagnostic medical imaging
• We have access to key opinion leaders across UK and internationally
22. Vaccines
Expertise:
• Experience of clinical trials with flu vaccines including Hib – bacteria causing
pneumonia and meningitis, H. influenzae disease – the main cause of meningitis,
Haemophilus Influenzae - Gram Negative coccobacillus causing serious invasive
disease in paediatrics & adults and non encapsulated ncHi – (non-typeable)
causes respiratory tract infections.
Capabilities:
• We have access to private isolation rooms in early phase clinical trial units
• Onorach China facility (proposed) will have specific vaccine study rooms
• We have good relationships with key opinion leaders and links with local and
Australian vaccine researchers
23. Renal Impairment
Expertise:
• Experience in clinical diagnostics, medical imaging and clinical research
• Involved in studies relating to continuous and intermittent dialysis for ARF and
use of dopamine in patients with renal dysfunction.
• Knowledge of peritoneal dialysis
Capabilities:
• Onorach have access to key opinion leaders UK and internationally
• We have access to haemodialysis and peritoneal dialysis patients for clinical trials
• Dundee has a large Renal unit and are very active in research studies
24. Medical Devices
Expertise:
• Involved for many years in a large range of medical device studies
• Theatre instruments, glucometers, filters for haemodialysis and plasmaphoresis,
sutures, wound-care products, ultrasound machines etc.
• Co-developed positive ventilation delivery system for lung scanning intensive care
patients
• Experience of medical device clinical trials in the US and UK
Capabilities:
• Onorach have access to a range of hospitals in the UK and internationally who
can participate in medical device clinical trials
25. Stem Cells
Expertise:
• Sits on the Scottish Stem Cell Special Interest Group and SRMIC who influence
Government policy & bid for stem cell research funding
• Acted as UK Medical Liaison for a German stem cell company and conducted
CTs with hospitals in the UK and Germany
• Experienced in setting up stem cell studies
• Member of the EUSTM (European Society for Translational Medicine)
• Senior CRA with 10 years experience including stem cell studies
Capabilities:
• We can offer specialist regulatory consultancy and stem cell study sites
in the UK
• We have access to both leading Scottish experts in stem cell studies as well as
other international research specialists
26. Other
We also have expertise across other areas including:
•Cardiac metabolic studies
•MS studies
•Rare diseases
•Orphan drugs
•Biomarker studies
•Vascular flow studies
•Opthalmics
•Dentistry
•Psychiatry
•Demographic studies
•Stability studies
28. Benefits to clients
• Improved clinical trials design using innovative services
• Internalizing of knowledge of how to meet FDA and other regulatory requirements
• Higher degree of confidence in preparation for GxP audits
• Accelerated patient/subject recruitment
• More effective conduct of clinical research studies
• Delivery of clinically relevant results
• Achieve faster completion of clinical trials than in-house CROs
• Better management of risk (clinical development & financial)
• More highly informed position regarding ‘go/no go’ for CT projects
29. Who we are (Onorach Management Team)
Managing Director
Professor Christene Leiper
Founding member of Onorach®
•Currently holds the position of Managing Director and is a major shareholder
•Professor in Medicine and Health Sciences at Bond University, Queensland, Australia
•Holds a PhD for research in Nuclear Medicine, awarded by the University of
Melbourne, Australia
•30-year career in the health industry, holding a variety of senior positions in contract
and clinical research organisations including GM Clinical, Glasgow; The University of
Edinburgh; Vita Medical, Australia
•Worked at Ninewells Hospital in Drug Development Solutions and played a key role
(at Scottish Government level) in Quality Assurance for the first Scottish National
Stroke Services Audit
•Senior Associate of the Royal Society of Medicine
• Member of the EUSTM (European Society for Translational Medicine)
30. Who we are
Chief Executive Officer
Stephen Leiper, B.Sc.
Co-founder of Onorach®
•Currently CEO and Director and a major shareholder
•Bachelor of Science degree from the University of Sydney, majoring in histology
•Senior Associate of the Royal Society of Medicine
•Proven track record of over 30 years success in sales and marketing to life sciences
organisations
•Areas of expertise include specialist sales of medical devices to surgeons in cardiac
operating theatres; enterprise level IT solutions for life science companies; cutting
edge molecular biology and tissue culture products
•Prior to setting up Onorach, Stephen was global business development manager for
GM Clinical, Glasgow
31. Who we are
Senior Projects Manager
Mandy Peden
Mandy Peden is a Pharmacist with 25 years’ experience in the pharmaceutical/biotech
industry and holds a Dip Clin Sci from Cardiff University, a postgraduate qualification
specifically for clinical research.
Mandy has extensive clinical monitoring experience, from Principal, Lead and Senior
Clinical Research Associate roles with skills in management and co-ordination of
clinical trials with both International Pharma and CRO companies.
Mandy has experience in training, protocol development, site management, data
monitoring, electronic data capture, auditing and reporting as well as being
accustomed to working and managing projects in highly regulated and fast-paced
environments.
32. Who we are
Global Marketing Manager
Martin E. Hunt, BSc (Hons)
Directing the branding, marketing and promotion of Onorach®
and it’s subsidiaries
world-wide.
•Career spanning 20 years, involving Quality Management, Organisational
Development and International Marketing disciplines.
•Worked in organisations from SMEs of less than 10 employees up to multi-national
blue-chip global entities.
•Diverse background in industries including Academia, Oil & Gas, Electronics,
Pharmaceutical Manufacturing, Clinical Trial Manufacturing and CRO.
•Experienced in the creation and management of new business start-up for a top 10
Pharmaceutical CMO.
•High degree of experience working in high-value, regulated industrial sectors.
•Other areas of expertise include quality auditing and employee performance system
design.