Brochure e-GCR Biopharma
•
2 likes•506 views
Most of clinical trials are delayed because recruitment rates do not meet expectations, due to the growing complexity of protocols. North Africa possesses all the features to be an interesting area for numerous clinical trials….. La plupart des essais cliniques sont annulés, à cause d’un taux de recrutement bas, qui ne satisfait pas les attentes. Cette baisse est due à une croissance de la complexité des projets de recherche. L’Afrique du Nord possède des atouts intéressants favorables pour le déroulement des essais cliniques….. http://www.e-gcr.com/
Report
Share
Report
Share
Download to read offline
Recommended
FDA Guidance and Clinical Trials
The Food and Drug Administration (FDA) released Clinical Trial Imaging Endpoint Process Standards guidance for clinical trials industry. Why? To standardize. To automate. To move closer to zero-delay clinical trials. Read AG Mednet's perspective on this FDA guidance.
Prosoft Clinical
Prosoft Clinical Services and Capabilities provides clinical trial services including CMC formulation development, biostatistics, data management, clinical operations, medical writing, and regulatory strategy and operations. They have experience across multiple therapeutic areas like allergy/respiratory, CNS, dermatology, heart failure, HIV, hypertension, oncology, pain, and women's health. Their team has extensive experience developing products through all phases of clinical trials and regulatory approval.
Actimus Biosciences
Actimus Biosciences Pvt Ltd is a clinical research organization founded in 2005 in Visakhapatnam, India. It is led by Chairman and Managing Director Ramnath Reddy, who has experience in the healthcare and pharmaceutical industries. The company has facilities for clinical trials including two clinics with 72 beds and laboratories equipped for bioanalytical work. It provides clinical trial services and has experience conducting over 350 studies.
Navigating Pharmacovigilance
1) Ashfield Pharmacovigilance provides pharmacovigilance services to ensure clients can focus on other areas of product development by smoothly navigating regulatory requirements.
2) The document outlines many regulatory changes to pharmacovigilance between 2012-2015 from organizations like EMA, FDA, and ICH.
3) Ashfield Pharmacovigilance has experts in compliance and regulatory solutions who monitor regulatory changes and provide services like case management, database hosting, and audit support across various therapeutic areas and product types.
Ashfield Pharmacovigilance
Ashfield Pharmacovigilance is a global leader in safety and risk management services supporting pharmaceutical, biotech, medical device, consumer health and animal health organizations.
Uniquely focused on pharmacovigilance, we provide outsourced solutions and modified services to augment existing safety departments.
Ashfield Pharmacovigilance has a unique advantage in drug safety and pharmacovigilance due to the high level of expertise across our case managers, project managers, quality and regulatory staff and database administrators. We allow you to focus on your core business, while we partner with you to promote patient safety and product longevity. We achieve this by fostering the open exchange of ideas among organizations throughout the pharmacovigilance community.
By delivering innovative approaches to global case management, aggregate report development, literature search services, signal detection and surveillance, risk management services, safety system implementation, and medical information and call center services, Ashfield Pharmacovigilance is helping to advance the practice of pharmacovigilance on a global scale.
Founded in 2000, we were acquired by UDG Healthcare in 2012 and are proud to be part of its Ashfield division.
Ashfield Pharmacovigilance is headquartered in Research Triangle Park, North Carolina. Learn more about us at www.ashfieldhealthcare.com and follow us on Twitter, @DSA_PV and LinkedIn.
About Ashfield Healthcare
Ashfield Commercial & Medical Services is the sales, marketing and medical arm of UDG Healthcare plc. Established in the UK in 1997, the division is comprised of eight areas of expertise with a history of providing outstanding, client-focused services.
These eight areas of expertise include medical information, pharmacovigilance, healthcare communications, contract sales, market research, leadership training, market access strategy and meeting and event planning. The division consists of more than 5,500 staff in 20 countries.
About UDG Healthcare
Headquartered in Dublin, Ireland, UDG Healthcare plc is a diverse, global healthcare solutions company with interests in healthcare supply chain management, special packaging, sales and marketing and medical services for life science companies.
Find out more http://www.ashfieldhealthcare.com
Just the Facts- Meaningful Use Stage 2 & ICD 10
Attend this hard hitting session where Rebecca Wiedmeyer, President of Vela Consulting Group will share her experiences helping hundreds of covered entities understand and address MU 2. In addition she will provide answers to the complexity of addressing ICD 10.
Panelists:
Rebecca Wiedmeyer, President of Vela Consulting Group
Moderator:
Marc Haskelson, President, The Compliancy Group LLC.
Sukraa lab presentation 2021-v1
Sukraa provides integrated business applications for hospitals and diagnostic centers around the world. It has over 15 years of experience in the healthcare industry and offices in Chennai, India housing over 30 software consultants. Sukraa's Laboratory Information System (SLIMS) is a web-based LIS that integrates all laboratory modules and interfaces with over 350 medical devices to generate 14 million patient records annually for its 250 clients globally.
CHRS Animal Health Brochure
This document discusses services for animal health product development provided by Cardinal Health Regulatory Sciences. They offer integrated scientific and regulatory strategies to help animal health companies get products to market faster and earn greater returns on investments. Their services include product development consulting, managing regulatory submissions and documentation, facility inspections, and post-approval support. With decades of experience in scientific and regulatory consulting, they can provide continuity of service from product development through approval and marketing.
Recommended
FDA Guidance and Clinical Trials
The Food and Drug Administration (FDA) released Clinical Trial Imaging Endpoint Process Standards guidance for clinical trials industry. Why? To standardize. To automate. To move closer to zero-delay clinical trials. Read AG Mednet's perspective on this FDA guidance.
Prosoft Clinical
Prosoft Clinical Services and Capabilities provides clinical trial services including CMC formulation development, biostatistics, data management, clinical operations, medical writing, and regulatory strategy and operations. They have experience across multiple therapeutic areas like allergy/respiratory, CNS, dermatology, heart failure, HIV, hypertension, oncology, pain, and women's health. Their team has extensive experience developing products through all phases of clinical trials and regulatory approval.
Actimus Biosciences
Actimus Biosciences Pvt Ltd is a clinical research organization founded in 2005 in Visakhapatnam, India. It is led by Chairman and Managing Director Ramnath Reddy, who has experience in the healthcare and pharmaceutical industries. The company has facilities for clinical trials including two clinics with 72 beds and laboratories equipped for bioanalytical work. It provides clinical trial services and has experience conducting over 350 studies.
Navigating Pharmacovigilance
1) Ashfield Pharmacovigilance provides pharmacovigilance services to ensure clients can focus on other areas of product development by smoothly navigating regulatory requirements.
2) The document outlines many regulatory changes to pharmacovigilance between 2012-2015 from organizations like EMA, FDA, and ICH.
3) Ashfield Pharmacovigilance has experts in compliance and regulatory solutions who monitor regulatory changes and provide services like case management, database hosting, and audit support across various therapeutic areas and product types.
Ashfield Pharmacovigilance
Ashfield Pharmacovigilance is a global leader in safety and risk management services supporting pharmaceutical, biotech, medical device, consumer health and animal health organizations.
Uniquely focused on pharmacovigilance, we provide outsourced solutions and modified services to augment existing safety departments.
Ashfield Pharmacovigilance has a unique advantage in drug safety and pharmacovigilance due to the high level of expertise across our case managers, project managers, quality and regulatory staff and database administrators. We allow you to focus on your core business, while we partner with you to promote patient safety and product longevity. We achieve this by fostering the open exchange of ideas among organizations throughout the pharmacovigilance community.
By delivering innovative approaches to global case management, aggregate report development, literature search services, signal detection and surveillance, risk management services, safety system implementation, and medical information and call center services, Ashfield Pharmacovigilance is helping to advance the practice of pharmacovigilance on a global scale.
Founded in 2000, we were acquired by UDG Healthcare in 2012 and are proud to be part of its Ashfield division.
Ashfield Pharmacovigilance is headquartered in Research Triangle Park, North Carolina. Learn more about us at www.ashfieldhealthcare.com and follow us on Twitter, @DSA_PV and LinkedIn.
About Ashfield Healthcare
Ashfield Commercial & Medical Services is the sales, marketing and medical arm of UDG Healthcare plc. Established in the UK in 1997, the division is comprised of eight areas of expertise with a history of providing outstanding, client-focused services.
These eight areas of expertise include medical information, pharmacovigilance, healthcare communications, contract sales, market research, leadership training, market access strategy and meeting and event planning. The division consists of more than 5,500 staff in 20 countries.
About UDG Healthcare
Headquartered in Dublin, Ireland, UDG Healthcare plc is a diverse, global healthcare solutions company with interests in healthcare supply chain management, special packaging, sales and marketing and medical services for life science companies.
Find out more http://www.ashfieldhealthcare.com
Just the Facts- Meaningful Use Stage 2 & ICD 10
Attend this hard hitting session where Rebecca Wiedmeyer, President of Vela Consulting Group will share her experiences helping hundreds of covered entities understand and address MU 2. In addition she will provide answers to the complexity of addressing ICD 10.
Panelists:
Rebecca Wiedmeyer, President of Vela Consulting Group
Moderator:
Marc Haskelson, President, The Compliancy Group LLC.
Sukraa lab presentation 2021-v1
Sukraa provides integrated business applications for hospitals and diagnostic centers around the world. It has over 15 years of experience in the healthcare industry and offices in Chennai, India housing over 30 software consultants. Sukraa's Laboratory Information System (SLIMS) is a web-based LIS that integrates all laboratory modules and interfaces with over 350 medical devices to generate 14 million patient records annually for its 250 clients globally.
CHRS Animal Health Brochure
This document discusses services for animal health product development provided by Cardinal Health Regulatory Sciences. They offer integrated scientific and regulatory strategies to help animal health companies get products to market faster and earn greater returns on investments. Their services include product development consulting, managing regulatory submissions and documentation, facility inspections, and post-approval support. With decades of experience in scientific and regulatory consulting, they can provide continuity of service from product development through approval and marketing.
Sharing Knowledge - Lab outsourcing/Managemeent
Tarek Shaker PMP, CPHQ is the Development & Training manager at Al Borg Laboratories in GCC and Africa. The document discusses laboratory outsourcing and its benefits. It notes that outsourcing laboratory management can reduce costs by up to 20% through efficiencies and economies of scale. Outsourcing also improves quality by applying international standards and gives access to advanced technology and capabilities. The Saudi Arabia Ministry of Health is increasing private sector participation in healthcare delivery through public-private partnerships to address challenges around access, quality, workforce and financial sustainability.
Final Slide Show - Ready for EquityNet
The document describes a company that has developed an automated glucose monitoring technology through 20 years of research. It has proven effective in clinical trials and holds several patents. The company is now seeking to license the technology to others to develop market solutions and bring the product to the global point-of-care monitoring market, which is in high demand and valued at $3 billion annually. The technology aims to improve patient outcomes and reduce healthcare costs by providing continuous, real-time glucose monitoring for critically ill patients. Investors are invited to help bring this solution to market by funding the company's marketing and licensing efforts.
DSA_Infographic_Final
The document discusses the complex regulatory landscape of pharmacovigilance and how DSA ensures a smooth journey for clients to focus on other crucial areas of product development. It lists several regulatory changes between 2012-2015 from agencies like EMA, FDA, and ICH. DSA provides compliance, regulation, and implementation solutions including a pharmacovigilance database hosted on Oracle platforms in a tier 3 data center. DSA employees are tenured life science or healthcare professionals with experience across therapeutic areas, products, and supporting over 11 global regulatory inspections.
A Pharma/CRO Partnership in the Design and Execution of Paperless Clinical Tr...
DIA 2019 presentation by Dr. Jules Mitchel with Michelle Eli (Lilly) and Tom Haag (ex-Novartis) based on their experience with Lilly collaborating on Target Health's paperless clinical trial system.
How eSource Solutions are Impacting Clinical Research Sites, Patients, Regula...
1) eSource solutions like electronic data capture and medical devices that directly transmit data are improving clinical trials by allowing real-time data review, fewer errors and violations, and remote monitoring. This benefits sites, patients, sponsors and regulators.
2) Metrics from several studies show that most data is entered within a few days and that centralized monitoring can review data very quickly, within hours. Few queries are needed and most involve simple corrections.
3) Presenters conclude that paperless trials using validated systems provide significant efficiencies and higher data quality and integrity for all stakeholders when properly implemented.
FDA Electronic Health Record Data in Clinical Research
Dr. Jules Mitchel, President of Target Health, delivered this presentation on the new FDA Guidance on the use of the electronic health record for clinical research at the North American eClinical Forum Autumn Meeting on October 2, 2018.
CHRS Biotechnology Brochure
Biotechnology, pharmaceutical, and medical device companies can partner with Cardinal Health Regulatory Sciences for additional resources and expertise throughout the biologics development process. Cardinal Health offers services including product development strategies, regulatory documentation preparation, facility inspections, and global regulatory strategies. Their experience includes over 100 product approvals across therapeutic areas. Partnering with Cardinal Health can help companies facilitate multinational approvals and achieve greater returns on development investments.
HospitalSoftwareShop - Laboratory Information System LIS
HospitalSoftwareShop provides exhaustive LIS Software - Laboratory Information System -for Pathology Labs. Being web-based makes lab software globally accessible. Software for labs offers widest range of pathology tests, direct integration with lab equipment without manual intervention reduces errors and time
4 benefits of a mobile app for the healthcare industry
This document outlines 4 key benefits of mobile apps for the healthcare industry: 1) Reduced risks of diagnostic errors by leveraging intelligent data and cloud storage of patient records, 2) Streamlining clinical processes by giving healthcare professionals access to patient information and data on smart devices, 3) Enabling immediate access to care by allowing patients to order medications remotely via mobile apps for delivery, 4) Catering to patient customization by allowing healthcare providers to quickly access patient health histories and customize treatment through customized mobile apps.
Javali
Javali is a technology that utilizes advanced text searching and data aggregation to improve clinical coding accuracy and completeness. It automatically scans patient records to identify missed complications, comorbidities, and procedures that would result in higher reimbursements. By more accurately identifying these codes, Javali helped one hospital increase inpatient revenues by £9 million in one year. It provides a unique solution that is able to extract additional coding opportunities even after other coding technologies and processes have been implemented.
Engineering for Connected Patients in the IoT Era
This document summarizes Anurag Singhal's presentation on engineering for connected patients in the IoT era. Singhal is the director of engineering at Clinical Ink, which provides mobile apps and a platform called CentrosHealth to enable clinical trials to capture data from patients using connected devices and sensors. The presentation discusses how Clinical Ink uses MongoDB to store diverse clinical trial and sensor data, ensuring data security, audit trails, and compliance with regulations. It also describes challenges around processing large volumes of data from wearable sensors and finding solutions to issues like data deduplication and streaming.
GS1 standards to save Barking, Havering & Redbridge University NHS Trust over...
Find out how they implemented GS1 standards for health records tracking.
http://www.gs1uk.org/healthcare
Corey Makes Healthcare - Coordinate, Efficient and Mobile
Core Mobile offers the Corey suite of products to coordinate healthcare activities in real-time and make them more efficient. The Corey products allow providers to update tasks on mobile devices, notify families of patient status, and access analytics and relevant patient information remotely. This increases OR utilization by 15-30% and reduces patient turnover times by 5-15 minutes, saving hospitals $1-10 million annually. Core Mobile's patented solutions integrate with existing IT systems and workflows to optimize provider coordination without disruption.
Healtho5 supported Medical Tele Consultation Centers in Bangladesh
Healtho5 Solutions is the technology partner for successfully running telemedicine projects with Border Guard Bangladesh. Here's a background on how our cloud based secure health information management system helps power telemedicine consultations for hundreds of thousands of patients in Bangladesh.
Cell & Gene Therapy Post-Approval Solutions
Cell & Gene Therapy post-approval solutions to reduce scientific, regulatory and commercial risks, and accelerate development wherever you are in your product's development.
Customer Needs
The SecureReg solution from LifeMed ID aims to improve the patient experience, operating efficiencies, and patient identification security. It has been implemented across multiple healthcare providers to 1) enhance the registration process at all points of care, 2) eliminate manual processes that can cause record errors or duplicates, and 3) guarantee the right patient is connected to the correct medical records each visit. A case study found one 25-bed hospital achieved over $300,000 in annual savings with an 8-month payback period through increased satisfaction, reduced admission times, diminished errors, lower accounts receivable, and staff reductions.
Ready, Set, Launch Invitation
This invitation-only conference focuses on pharmacovigilance challenges associated with successful product launches. It will provide industry experts discussing changes in regulatory requirements pre- and post-approval, organizational frameworks for post-marketing pharmacovigilance, and pharmacovigilance and market access considerations prior to product acquisition. The event is designed to enhance knowledge of differences in pharmacovigilance requirements when transitioning from clinical to post-approval stages or launching newly acquired products. It will take place on November 3, 2015 in Durham, North Carolina and is aimed at heads of medical affairs, regulatory professionals, chief safety and medical officers, and those with pharmacovigilance or product launch responsibilities.
Real-Time Data. Real-World Impact Brochure
Find eligible patients that fit your protocol faster, identify and secure proven and/or new sites, forecast and measure progress more efficiency. With Covance's proprietary data, your program hits its mark.
2019-DMFR PPTeeeeeeeeeeeeeeeeeeeeeee.pptx
Worldclass Diagnostic Healthcare provides pathology, cardiology, radiology, and wellness services using next generation technology. It aims to deliver accurate diagnostic reports through expert assistance and a scientific logistics approach. The company utilizes state-of-the-art technology and quality control programs to provide error-free diagnosis and reduce treatment time. It has various specialized experts and infrastructure to improve patient care.
Popsi Cube 2011
We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications specific to the pharmaceutical industry.
BioKinetic Profile.docx
BioKinetic Europe is a clinical research organization celebrating its 20th anniversary of conducting clinical trials in Northern Ireland. It has significant experience managing Phase I-III trials for pharmaceutical companies. Recently, BioKinetic invested in a new electronic data capture system called ALPHADAS to improve efficiency and reduce monitoring costs. As an experienced CRO located in Northern Ireland with strong university partnerships, BioKinetic provides flexible and high-quality clinical trial services to pharmaceutical and biotech clients.
Cns clinical trials (2010)
This document provides information about the "CNS Clinical Trials" conference taking place on September 16-17, 2010 in London. The conference will examine strategies for successful CNS drug development and overcoming challenges in clinical trial design, management, and recruitment. Key topics will include novel cognitive assessment methods, advances in neuroimaging, adaptive trial design, and the use of biomarkers to demonstrate early drug effects in CNS trials. Speakers will include representatives from pharmaceutical and biotechnology companies as well as academic institutions. Attendees will gain insights on improving various aspects of CNS clinical trials from development through regulatory approval. The conference also provides sponsorship and exhibition opportunities for companies to promote their products and services.
More Related Content
What's hot
Sharing Knowledge - Lab outsourcing/Managemeent
Tarek Shaker PMP, CPHQ is the Development & Training manager at Al Borg Laboratories in GCC and Africa. The document discusses laboratory outsourcing and its benefits. It notes that outsourcing laboratory management can reduce costs by up to 20% through efficiencies and economies of scale. Outsourcing also improves quality by applying international standards and gives access to advanced technology and capabilities. The Saudi Arabia Ministry of Health is increasing private sector participation in healthcare delivery through public-private partnerships to address challenges around access, quality, workforce and financial sustainability.
Final Slide Show - Ready for EquityNet
The document describes a company that has developed an automated glucose monitoring technology through 20 years of research. It has proven effective in clinical trials and holds several patents. The company is now seeking to license the technology to others to develop market solutions and bring the product to the global point-of-care monitoring market, which is in high demand and valued at $3 billion annually. The technology aims to improve patient outcomes and reduce healthcare costs by providing continuous, real-time glucose monitoring for critically ill patients. Investors are invited to help bring this solution to market by funding the company's marketing and licensing efforts.
DSA_Infographic_Final
The document discusses the complex regulatory landscape of pharmacovigilance and how DSA ensures a smooth journey for clients to focus on other crucial areas of product development. It lists several regulatory changes between 2012-2015 from agencies like EMA, FDA, and ICH. DSA provides compliance, regulation, and implementation solutions including a pharmacovigilance database hosted on Oracle platforms in a tier 3 data center. DSA employees are tenured life science or healthcare professionals with experience across therapeutic areas, products, and supporting over 11 global regulatory inspections.
A Pharma/CRO Partnership in the Design and Execution of Paperless Clinical Tr...
DIA 2019 presentation by Dr. Jules Mitchel with Michelle Eli (Lilly) and Tom Haag (ex-Novartis) based on their experience with Lilly collaborating on Target Health's paperless clinical trial system.
How eSource Solutions are Impacting Clinical Research Sites, Patients, Regula...
1) eSource solutions like electronic data capture and medical devices that directly transmit data are improving clinical trials by allowing real-time data review, fewer errors and violations, and remote monitoring. This benefits sites, patients, sponsors and regulators.
2) Metrics from several studies show that most data is entered within a few days and that centralized monitoring can review data very quickly, within hours. Few queries are needed and most involve simple corrections.
3) Presenters conclude that paperless trials using validated systems provide significant efficiencies and higher data quality and integrity for all stakeholders when properly implemented.
FDA Electronic Health Record Data in Clinical Research
Dr. Jules Mitchel, President of Target Health, delivered this presentation on the new FDA Guidance on the use of the electronic health record for clinical research at the North American eClinical Forum Autumn Meeting on October 2, 2018.
CHRS Biotechnology Brochure
Biotechnology, pharmaceutical, and medical device companies can partner with Cardinal Health Regulatory Sciences for additional resources and expertise throughout the biologics development process. Cardinal Health offers services including product development strategies, regulatory documentation preparation, facility inspections, and global regulatory strategies. Their experience includes over 100 product approvals across therapeutic areas. Partnering with Cardinal Health can help companies facilitate multinational approvals and achieve greater returns on development investments.
HospitalSoftwareShop - Laboratory Information System LIS
HospitalSoftwareShop provides exhaustive LIS Software - Laboratory Information System -for Pathology Labs. Being web-based makes lab software globally accessible. Software for labs offers widest range of pathology tests, direct integration with lab equipment without manual intervention reduces errors and time
4 benefits of a mobile app for the healthcare industry
This document outlines 4 key benefits of mobile apps for the healthcare industry: 1) Reduced risks of diagnostic errors by leveraging intelligent data and cloud storage of patient records, 2) Streamlining clinical processes by giving healthcare professionals access to patient information and data on smart devices, 3) Enabling immediate access to care by allowing patients to order medications remotely via mobile apps for delivery, 4) Catering to patient customization by allowing healthcare providers to quickly access patient health histories and customize treatment through customized mobile apps.
Javali
Javali is a technology that utilizes advanced text searching and data aggregation to improve clinical coding accuracy and completeness. It automatically scans patient records to identify missed complications, comorbidities, and procedures that would result in higher reimbursements. By more accurately identifying these codes, Javali helped one hospital increase inpatient revenues by £9 million in one year. It provides a unique solution that is able to extract additional coding opportunities even after other coding technologies and processes have been implemented.
Engineering for Connected Patients in the IoT Era
This document summarizes Anurag Singhal's presentation on engineering for connected patients in the IoT era. Singhal is the director of engineering at Clinical Ink, which provides mobile apps and a platform called CentrosHealth to enable clinical trials to capture data from patients using connected devices and sensors. The presentation discusses how Clinical Ink uses MongoDB to store diverse clinical trial and sensor data, ensuring data security, audit trails, and compliance with regulations. It also describes challenges around processing large volumes of data from wearable sensors and finding solutions to issues like data deduplication and streaming.
GS1 standards to save Barking, Havering & Redbridge University NHS Trust over...
Find out how they implemented GS1 standards for health records tracking.
http://www.gs1uk.org/healthcare
Corey Makes Healthcare - Coordinate, Efficient and Mobile
Core Mobile offers the Corey suite of products to coordinate healthcare activities in real-time and make them more efficient. The Corey products allow providers to update tasks on mobile devices, notify families of patient status, and access analytics and relevant patient information remotely. This increases OR utilization by 15-30% and reduces patient turnover times by 5-15 minutes, saving hospitals $1-10 million annually. Core Mobile's patented solutions integrate with existing IT systems and workflows to optimize provider coordination without disruption.
Healtho5 supported Medical Tele Consultation Centers in Bangladesh
Healtho5 Solutions is the technology partner for successfully running telemedicine projects with Border Guard Bangladesh. Here's a background on how our cloud based secure health information management system helps power telemedicine consultations for hundreds of thousands of patients in Bangladesh.
Cell & Gene Therapy Post-Approval Solutions
Cell & Gene Therapy post-approval solutions to reduce scientific, regulatory and commercial risks, and accelerate development wherever you are in your product's development.
Customer Needs
The SecureReg solution from LifeMed ID aims to improve the patient experience, operating efficiencies, and patient identification security. It has been implemented across multiple healthcare providers to 1) enhance the registration process at all points of care, 2) eliminate manual processes that can cause record errors or duplicates, and 3) guarantee the right patient is connected to the correct medical records each visit. A case study found one 25-bed hospital achieved over $300,000 in annual savings with an 8-month payback period through increased satisfaction, reduced admission times, diminished errors, lower accounts receivable, and staff reductions.
Ready, Set, Launch Invitation
This invitation-only conference focuses on pharmacovigilance challenges associated with successful product launches. It will provide industry experts discussing changes in regulatory requirements pre- and post-approval, organizational frameworks for post-marketing pharmacovigilance, and pharmacovigilance and market access considerations prior to product acquisition. The event is designed to enhance knowledge of differences in pharmacovigilance requirements when transitioning from clinical to post-approval stages or launching newly acquired products. It will take place on November 3, 2015 in Durham, North Carolina and is aimed at heads of medical affairs, regulatory professionals, chief safety and medical officers, and those with pharmacovigilance or product launch responsibilities.
Real-Time Data. Real-World Impact Brochure
Find eligible patients that fit your protocol faster, identify and secure proven and/or new sites, forecast and measure progress more efficiency. With Covance's proprietary data, your program hits its mark.
What's hot (18)
A Pharma/CRO Partnership in the Design and Execution of Paperless Clinical Tr...
A Pharma/CRO Partnership in the Design and Execution of Paperless Clinical Tr...
How eSource Solutions are Impacting Clinical Research Sites, Patients, Regula...
How eSource Solutions are Impacting Clinical Research Sites, Patients, Regula...
FDA Electronic Health Record Data in Clinical Research
FDA Electronic Health Record Data in Clinical Research
HospitalSoftwareShop - Laboratory Information System LIS
HospitalSoftwareShop - Laboratory Information System LIS
4 benefits of a mobile app for the healthcare industry
4 benefits of a mobile app for the healthcare industry
GS1 standards to save Barking, Havering & Redbridge University NHS Trust over...
GS1 standards to save Barking, Havering & Redbridge University NHS Trust over...
Corey Makes Healthcare - Coordinate, Efficient and Mobile
Corey Makes Healthcare - Coordinate, Efficient and Mobile
Healtho5 supported Medical Tele Consultation Centers in Bangladesh
Healtho5 supported Medical Tele Consultation Centers in Bangladesh
Similar to Brochure e-GCR Biopharma
2019-DMFR PPTeeeeeeeeeeeeeeeeeeeeeee.pptx
Worldclass Diagnostic Healthcare provides pathology, cardiology, radiology, and wellness services using next generation technology. It aims to deliver accurate diagnostic reports through expert assistance and a scientific logistics approach. The company utilizes state-of-the-art technology and quality control programs to provide error-free diagnosis and reduce treatment time. It has various specialized experts and infrastructure to improve patient care.
Popsi Cube 2011
We have a unique profile for a CRO providing distinctive and innovative dual expertise by combining clinical research implementation with the development of customized IT applications specific to the pharmaceutical industry.
BioKinetic Profile.docx
BioKinetic Europe is a clinical research organization celebrating its 20th anniversary of conducting clinical trials in Northern Ireland. It has significant experience managing Phase I-III trials for pharmaceutical companies. Recently, BioKinetic invested in a new electronic data capture system called ALPHADAS to improve efficiency and reduce monitoring costs. As an experienced CRO located in Northern Ireland with strong university partnerships, BioKinetic provides flexible and high-quality clinical trial services to pharmaceutical and biotech clients.
Cns clinical trials (2010)
This document provides information about the "CNS Clinical Trials" conference taking place on September 16-17, 2010 in London. The conference will examine strategies for successful CNS drug development and overcoming challenges in clinical trial design, management, and recruitment. Key topics will include novel cognitive assessment methods, advances in neuroimaging, adaptive trial design, and the use of biomarkers to demonstrate early drug effects in CNS trials. Speakers will include representatives from pharmaceutical and biotechnology companies as well as academic institutions. Attendees will gain insights on improving various aspects of CNS clinical trials from development through regulatory approval. The conference also provides sponsorship and exhibition opportunities for companies to promote their products and services.
CPGR - Service provision, innovation eco-system creation, translational resea...
The CPGR provides genomic and proteomic services and conducts translational research and development. It was established in 2006 in Cape Town, South Africa to support the development of an internationally competitive bioeconomy. The CPGR maintains state-of-the-art genomic and proteomic technologies and bioinformatics capabilities to provide services and collaborate on research projects. It aims to stimulate life science innovation in Africa through creating an innovation ecosystem and building genomic and proteomic capacity.
Enterprise Clinical Solutions
Clinical trials have become more complex over the years as therapies and development models have evolved. The costs of delayed and prolonged clinical trials can be high. Digital adoption in trials has increased but there are still challenges to widespread adoption. Indegene aims to simplify clinical development lifecycles in order to drive faster decisions, predictable success, and bring innovative therapies to patients more quickly through proven trial acceleration solutions and end-to-end management of trial operations.
Customized Oncology Development Solutions: Clinical Trials Designed Around You®
Covance provides customized clinical trial solutions and services for oncology drug development. Their services include utilizing patient lab data to assess trial feasibility and identify eligible patients, scientific consultation in precision medicine areas, and selecting investigator sites with the right patients and experience. Covance aims to help clients accelerate development timelines, improve the probability of success, and deliver trials on budget.
Healthcare IT@ACGIL.ppt
"Electra HIS" is developed & promoted by ACG Infotech Limited, a NASSCOM Company under the guidance of professional medical doctors. Electra HIS, is fully integrated and possesses the ability to share and exchange information across the platforms in real time and make the hospital paperless. Electra HIS is multi-location application complied with following Standards.
Brochure
Farm is an ISO 13485-certified and FDA-compliant product development consultancy with over 40 years of experience helping medical, life sciences, and consumer healthcare companies. It offers expertise in areas like user research, engineering, design, and regulatory compliance. Farm helps clients design devices that are safe, easy to use and effective by employing research, usability testing, and a process-driven development approach.
Image Core Lab _ www.imagecorelab.com
Corporate Deck . Image Core Lab . Image Management Services. Protocol Development, Core Image Labs, Clinical Trial Technologies, RECIST 11.1 , CHESON, Volumetric Analysis, Medical Expertise and Consultation,Study and Read Design,Site Identification,Site Training and Management
Clinical Monitoring imaging aspects,Image Management
Reliable and Secure Data Management,Read Execution
Data Delivery,Medical Writing. Multi Modality. Multi Specialty - Oncology,Cardiology,Neurology,Rheumatology,Pulmonary
Cliniminds- Skill Development Program in Pharmacovigilance
CLINIMINDS brings to you an intensive course covering all the aspects of case processing, specially designed for Pharmacovigilance professional.
Our training program involves:
1. Fresher training for Drug Safety Associate with Hands On experience on safety database
2. Training on Case Processing
3. Training on Aggregate Reporting with Hands On
experience in PSUR/ PBRER writing
4. Training on Signal Detection and Risk Management
5. Training on Regulatory Affairs on Audits
6. Training Medical and Scientific Content Writing
7. Customized Training on Pharmacovigilance (Designed exclusively for Corporate who need domain knowledge on specific area (s) of pharmacovigilance)
Brochure
Genelife Clinical Research is a technologically advanced CRO that aims to reduce drug development timelines through high quality services. It provides comprehensive clinical trial services from early phase to late phase trials across multiple therapeutic areas globally. Genelife utilizes experienced professionals and innovative tools to efficiently manage projects and ensure quality and regulatory compliance. Its goal is to become the most respected partner in providing product development and meeting unmet clinical research needs.
Content for PPT.docx
Amit Sharma
Role: Founder & CEO
Qualifications: MBA in Technology Management
Brief Bio: With over 15 years in healthcare technology, Amit founded DigiPath Solutions to revolutionize anatomical pathology through digital innovation. His visionary leadership has driven the company's growth and commitment to excellence.
Priya Kapoor
Role: Chief Operating Officer
Qualifications: MSc in Operations Management
Brief Bio: Priya brings extensive experience in operational excellence, ensuring seamless implementation of digital pathology solutions. Her strategic insights and commitment to efficiency contribute to the company's success.
Rajiv Verma
Role: Chief Technology Officer
Qualifications: PhD in Computer Science
Brief Bio: Rajiv leads our technology initiatives, leveraging his expertise in artificial intelligence and pathology informatics. His innovative approach drives the development of cutting-edge solutions for improved diagnostic precision.
Title: Key Contributors
1. Sneha Desai
Role: Lead Pathologist
Qualifications: MD in Pathology
Brief Bio: Dr. Sneha brings a wealth of clinical experience, ensuring the alignment of our digital solutions with the needs of pathologists. Her dedication to advancing pathology practices enhances the impact of our services.
2. Vivek Patel
Role: Senior Software Engineer
Qualifications: BTech in Computer Science
Brief Bio: Vivek is a key member of our software development team, contributing his technical expertise to create robust and user-friendly digital pathology solutions. His passion for innovation drives our technological advancements.
Title: Advisory Board
1. Dr. Meera Kapoor
Role: Medical Advisor
Qualifications: MD, Pathology
Brief Bio: Dr. Meera Kapoor provides invaluable medical insights, ensuring the clinical relevance of our solutions. Her distinguished career in pathology enhances our commitment to delivering high-quality healthcare technology.
2. Rahul Singhania
Role: Business Strategy Advisor
Qualifications: MBA in Strategy and Marketing
Brief Bio: Rahul guides our business strategies with a focus on market trends and customer needs. His expertise in strategic planning contributes to the company's sustainable growth.
lyscaut_corp leaflet_06-2016_v3_LR
Clinical trial imaging involves highly regulated and complex processes from image acquisition to analysis. Poor image quality can exclude patients who otherwise meet study criteria. Imaging allows evaluation of drug behavior in vivo including pharmacokinetics. An independent imaging company like Lyscaut provides uniform image handling, expert reader selection and adjudication, and resolves issues. Lyscaut offers both imaging and clinical support to integrate data efficiently and lower costs compared to using multiple companies.
Progamma Us
ProGammaScience Corporation is a consulting firm based in Montreal that has been providing quality assurance, regulatory affairs, and technical operations services to the pharmaceutical industry since 1985, including assistance with submissions, GMP compliance, analytical method validation, product development, and technical training. The company aims to deliver excellent client service and documentation support at the best possible cost through its team of qualified professionals. Some of ProGammaScience's clients include major pharmaceutical companies like Abbott, AstraZeneca, Merck, Novartis, and Pfizer.
Corporate Profile and Integrated Health Network
Pragmedic aims to transform healthcare through information management technology by creating a seamless continuum of care. Its mission is to become a market leader in healthcare software through leveraging IT to integrate consumers and providers. Pragmedic offers various solutions including an electronic health record, practice management, transcription services, and a healthcare community management solution to improve operational performance with minimal implementation and training requirements.
Kuantum Cro St V021
This document provides an overview of Kuantum, a clinical research organization in Turkey. It outlines the company's mission, values, goals, organizational structure, teams, therapeutic areas of expertise, and current projects. The mission is to become a leading clinical research service provider in Turkey and neighboring regions. Key values include integrity, respect, customer focus, innovation, and quality. Goals include meeting customer expectations, improving efficiency, and developing the company. The organizational structure includes clinical trials, logistics, administrative, and quality assurance groups. Current ongoing projects cover therapeutic areas such as oncology, cardiology, and immunology. Future plans include expanding facilities and services.
Group4_Week10_Final_Business_Plan_VERSION_8(1)
Nommas Life Sciences is developing diagnostic tests using proprietary lambody technology to detect various cancers. Their first product, NCDK, will be a point-of-care ELISA-like kit that can detect multiple cancers from a single patient sample. Nommas aims to raise $750,000 over 2 years to further develop their platform and commercialize NCDK. If successful, NCDK will fulfill an unmet need in cancer diagnostics and help Nommas become a leader in the field of precision oncology diagnostics. However, Nommas faces competition from large companies and must overcome regulatory hurdles to achieve commercial success.
DEC 3 2015 Mats Sundgren
1) The EHR4CR project developed a platform to facilitate clinical research by enabling access to de-identified patient health records across countries, systems, and sites.
2) The platform supports protocol feasibility testing, patient recruitment, and data capture/exchange through a network of hospitals in multiple European countries.
3) Going forward, the EHR4CR Champion Program aims to further validate and scale up the platform through partnerships with additional hospitals and research organizations, overseen by the newly formed European Institute for Innovation through Health Data.
The Rose Research Center Brochure
The Rose Research Center is a state-of-the-art clinical research facility with two locations in North Carolina specializing in tobacco dependence research. Led by Dr. Jed Rose, the Center employs experienced staff and uses advanced technology and equipment to conduct smoking, nicotine, and cessation clinical trials from early phase to late phase. The Center aims to develop alternatives to cigarette smoking and eliminate tobacco-related disease through innovative research.
Similar to Brochure e-GCR Biopharma (20)
CPGR - Service provision, innovation eco-system creation, translational resea...
CPGR - Service provision, innovation eco-system creation, translational resea...
Customized Oncology Development Solutions: Clinical Trials Designed Around You®
Customized Oncology Development Solutions: Clinical Trials Designed Around You®
Cliniminds- Skill Development Program in Pharmacovigilance
Cliniminds- Skill Development Program in Pharmacovigilance
Recently uploaded
Journal Article Review on Rasamanikya
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central
Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa CentralClinic ^%[+27633867063*Abortion Pills For Sale In Tembisa CentralClinic ^%[+27633867063*Abortion Pills For Sale In Tembisa CentralClinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central
Osteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Top 10 Best Ayurvedic Kidney Stone Syrups in India
we have mentioned the best 10 ayurvedic Kidney Stone Syrups. You can check all these products and choose the best one for yourself.
Top-Vitamin-Supplement-Brands-in-India List
Swisschem Dermacare provides the Top 10 Vitamin Supplement Brands in India. To know more about us give us call at our official number
Ketone bodies and metabolism-biochemistry
This slide consists of all the topics of ketone . This can be used for exam purpose for writing about Diabetic keto acidosis etc . Thank you
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by Stamler, Verified Chapters 1 - 33, Complete Newest Version Community Health Nursing A Canadian Perspective, 5th Edition by Stamler, Verified Chapters 1 - 33, Complete Newest Version Community Health Nursing A Canadian Perspective, 5th Edition by Stamler Community Health Nursing A Canadian Perspective, 5th Edition TEST BANK by Stamler Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Pdf Chapters Download Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Pdf Download Stuvia Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Study Guide Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Ebook Download Stuvia Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Questions and Answers Quizlet Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Studocu Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Quizlet Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Pdf Chapters Download Community Health Nursing A Canadian Perspective, 5th Edition Pdf Download Course Hero Community Health Nursing A Canadian Perspective, 5th Edition Answers Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Ebook Download Course hero Community Health Nursing A Canadian Perspective, 5th Edition Questions and Answers Community Health Nursing A Canadian Perspective, 5th Edition Studocu Community Health Nursing A Canadian Perspective, 5th Edition Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Pdf Chapters Download Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Pdf Download Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Study Guide Questions and Answers Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Ebook Download Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Questions Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Studocu Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Stuvia
Top Effective Soaps for Fungal Skin Infections in India
Swisschem Dermacare has mentioned the List of The Best Antifungal Soap In India 2022. All of these soaps are trusted by various Dermatology Experts.
A Classical Text Review on Basavarajeeyam
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Role of Mukta Pishti in the Management of Hyperthyroidism
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
In some case, your chronic prostatitis may be related to over-masturbation. Generally, natural medicine Diuretic and Anti-inflammatory Pill can help mee get a cure.
Histololgy of Female Reproductive System.pptx
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
Recently uploaded (20)
Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central
Clinic ^%[+27633867063*Abortion Pills For Sale In Tembisa Central
Osteoporosis - Definition , Evaluation and Management .pdf
Osteoporosis - Definition , Evaluation and Management .pdf
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
Hemodialysis: Chapter 4, Dialysate Circuit - Dr.Gawad
Top 10 Best Ayurvedic Kidney Stone Syrups in India
Top 10 Best Ayurvedic Kidney Stone Syrups in India
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
Ear and its clinical correlations By Dr. Rabia Inam Gandapore.pptx
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...
Top Effective Soaps for Fungal Skin Infections in India
Top Effective Soaps for Fungal Skin Infections in India
Role of Mukta Pishti in the Management of Hyperthyroidism
Role of Mukta Pishti in the Management of Hyperthyroidism
Vestibulocochlear Nerve by Dr. Rabia Inam Gandapore.pptx
Vestibulocochlear Nerve by Dr. Rabia Inam Gandapore.pptx
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...
Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
Does Over-Masturbation Contribute to Chronic Prostatitis.pptx
Brochure e-GCR Biopharma
- 2. Our Vision Most of clinical trials are delayed because recruitment rates do not meet expectations, due to the growing complexity of protocols. North Africa possesses all the features to be an intersting area for numerous clinical trials: Potential of recruitment in different therapeutic areas Reduced cost for the development Quality of its centres and investigators Geographical location close to European laboratories Internet is the main solution to attract the patients, who are looking for explanation about their diseases, eventually the results of clinical trials. e-GCR Biopharma put internet as his backbone, to popularize the clinical trial information for the patients and fast of execution for the professionals. For more information: info@e-gcr.com
- 3. Our Mission e-GCR Biopharma, your optimum partner is a Contract Research Organisation (CRO), located in Algeria. e-GCR Biopharma provides a complete range of clinical trials services to the medical institutions, pharmaceutical and biotechnology companies. By its Know-How techniques and outstanding services quality, e-GCR Biopharma helps you to reduce time, risk ans cost associated with the development and marketing of your new products. Our Services Study feasibility Project Management Clinical Operations Pharmacovigilance Medical Writing Document Management Clinical Monitoring Data Management Information Technology Quality Assurance Electronic Publishing Regulatory Affairs Logistic Assistance Patient Management For more information: info@e-gcr.com
- 4. w wegro w . ccm - . i o egro n @ -ccm f .